two N-terminal Tags, His-tag and T7-tag Antibody
two N-terminal Tags, His-tag and T7-tag Antibody
![]() pLanYFP-NT(N terminal tag) |
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ABP-FP-YNNCS | Allele Biotech | 5 ug | Ask for price |
![]() pmWasabi-NT(N terminal tag) |
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ABP-FP-WNNCS | Allele Biotech | 5 ug | Ask for price |
![]() pmTFP1-NT(N terminal tag)-PuroR |
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ABP-FP-TNNCSP | Allele Biotech | 5 ug | Ask for price |
![]() pLanRFP-NT(N terminal tag)-PuroR |
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ABP-FP-RNNCSP | Allele Biotech | 5 ug | Ask for price |
![]() pLanYFP-NT(N terminal tag)-PuroR |
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ABP-FP-YNNCSP | Allele Biotech | 5 ug | Ask for price |
![]() pmWasabi-NT(N terminal tag)-PuroR |
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ABP-FP-WNNCSP | Allele Biotech | 5 ug | Ask for price |
![]() pmTFP1-CT(C terminal tag) |
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ABP-FP-TCNCS | Allele Biotech | 5 ug | Ask for price |
![]() pLanRFP-CT(C terminal tag) |
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ABP-FP-RCNCS | Allele Biotech | 5 ug | Ask for price |
![]() pLanYFP-CT(C terminal tag) |
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ABP-FP-YCNCS | Allele Biotech | 5 ug | Ask for price |
![]() pmWasabi-CT(C terminal tag) |
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ABP-FP-WCNCS | Allele Biotech | 5 ug | Ask for price |
![]() pmTFP1-CT(C terminal tag)-PuroR |
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ABP-FP-TCNCSP | Allele Biotech | 5 ug | Ask for price |
![]() pLanRFP-CT(C terminal tag)-PuroR |
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ABP-FP-RCNCSP | Allele Biotech | 5 ug | Ask for price |
![]() pLanYFP-CT(C terminal tag)-PuroR |
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ABP-FP-YCNCSP | Allele Biotech | 5 ug | Ask for price |
![]() pmWasabi-CT(C terminal tag)-PuroR |
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ABP-FP-WCNCSP | Allele Biotech | 5 ug | Ask for price |
![]() Parathyroid Hormone Antibody / N Terminal |
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V3375-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: PTH/Parathyroid hormone is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V3375-20UG | NSJ Bioreagents | 20 ug | 153.3 EUR |
Description: PTH/Parathyroid hormone is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V3375SAF-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: PTH/Parathyroid hormone is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V3644-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: PTH/Parathyroid hormone is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V3644-20UG | NSJ Bioreagents | 20 ug | 153.3 EUR |
Description: PTH/Parathyroid hormone is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V3644IHC-7ML | NSJ Bioreagents | 7 ml | 349.3 EUR |
Description: PTH/Parathyroid hormone is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V3644SAF-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: PTH/Parathyroid hormone is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V3645-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: PTH/Parathyroid hormone is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V3645-20UG | NSJ Bioreagents | 20 ug | 153.3 EUR |
Description: PTH/Parathyroid hormone is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V3645IHC-7ML | NSJ Bioreagents | 7 ml | 349.3 EUR |
Description: PTH/Parathyroid hormone is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V3645SAF-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: PTH/Parathyroid hormone is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V3765-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Parathyroid hormone (PTH), parathormone or parathyrin, is secreted by the chief cells of the parathyroid glands as a polypeptide containing 84 amino acids, yet effective hormone-receptor interaction requires solely the 34-N-terminal amino acids. While PTH acts to increase the concentration of ionic calcium (Ca2+) in the blood, calcitonin, a hormone produced by the parafollicular cells (C cells) of the thyroid gland, acts to decrease ionic calcium concentration. [Wiki] |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V3765-20UG | NSJ Bioreagents | 20 ug | 153.3 EUR |
Description: Parathyroid hormone (PTH), parathormone or parathyrin, is secreted by the chief cells of the parathyroid glands as a polypeptide containing 84 amino acids, yet effective hormone-receptor interaction requires solely the 34-N-terminal amino acids. While PTH acts to increase the concentration of ionic calcium (Ca2+) in the blood, calcitonin, a hormone produced by the parafollicular cells (C cells) of the thyroid gland, acts to decrease ionic calcium concentration. [Wiki] |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V3765IHC-7ML | NSJ Bioreagents | 7 ml | 349.3 EUR |
Description: Parathyroid hormone (PTH), parathormone or parathyrin, is secreted by the chief cells of the parathyroid glands as a polypeptide containing 84 amino acids, yet effective hormone-receptor interaction requires solely the 34-N-terminal amino acids. While PTH acts to increase the concentration of ionic calcium (Ca2+) in the blood, calcitonin, a hormone produced by the parafollicular cells (C cells) of the thyroid gland, acts to decrease ionic calcium concentration. [Wiki] |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V3765SAF-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Parathyroid hormone (PTH), parathormone or parathyrin, is secreted by the chief cells of the parathyroid glands as a polypeptide containing 84 amino acids, yet effective hormone-receptor interaction requires solely the 34-N-terminal amino acids. While PTH acts to increase the concentration of ionic calcium (Ca2+) in the blood, calcitonin, a hormone produced by the parafollicular cells (C cells) of the thyroid gland, acts to decrease ionic calcium concentration. [Wiki] |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V7272-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: PTH/Parathyroid hormone is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V7272-20UG | NSJ Bioreagents | 20 ug | 153.3 EUR |
Description: PTH/Parathyroid hormone is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V7272IHC-7ML | NSJ Bioreagents | 7 ml | 349.3 EUR |
Description: PTH/Parathyroid hormone is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V7272SAF-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: PTH/Parathyroid hormone is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V2806-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: PTH is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V2806-20UG | NSJ Bioreagents | 20 ug | 153.3 EUR |
Description: PTH is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V2806IHC-7ML | NSJ Bioreagents | 7 ml | 349.3 EUR |
Description: PTH is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V2806SAF-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: PTH is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V2807-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Epitope of this mAb maps in the N-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V2807-20UG | NSJ Bioreagents | 20 ug | 153.3 EUR |
Description: Epitope of this mAb maps in the N-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V2807IHC-7ML | NSJ Bioreagents | 7 ml | 349.3 EUR |
Description: Epitope of this mAb maps in the N-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V2807SAF-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: Epitope of this mAb maps in the N-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V2808-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: PTH is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V2808-20UG | NSJ Bioreagents | 20 ug | 153.3 EUR |
Description: PTH is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V2808IHC-7ML | NSJ Bioreagents | 7 ml | 349.3 EUR |
Description: PTH is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody / N Terminal |
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V2808SAF-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: PTH is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Anti-Gasdermin D (N terminal) Antibody |
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ER1901-37 | HUABIO | 100ul | 189 EUR |
Description: Gasdermin-D, N-terminal: Promotes pyroptosis in response to microbial infection and danger signals. Produced by the cleavage of gasdermin-D by inflammatory caspases CASP1 or CASP4 in response to canonical, as well as non-canonical (such as cytosolic LPS) inflammasome activators. After cleavage, moves to the plasma membrane where it strongly binds to inner leaflet lipids, including monophosphorylated phosphatidylinositols, such as phosphatidylinositol 4-phosphate, bisphosphorylated phosphatidylinositols, such as phosphatidylinositol (4,5)-bisphosphate, as well as phosphatidylinositol (3,4,5)-bisphosphate, and more weakly to phosphatidic acid and phosphatidylserine. Homooligomerizes within the membrane and forms pores of 10 - 15 nanometers (nm) of inner diameter, possibly allowing the release of mature IL1B and triggering pyroptosis . Exhibits bactericidal activity. Gasdermin-D, N-terminal released from pyroptotic cells into the extracellular milieu rapidly binds to and kills both Gram-negative and Gram-positive bacteria, without harming neighboring mammalian cells, as it does not disrupt the plasma membrane from the outside due to lipid-binding specificity. |
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![]() T7 tag Antibody |
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39276-100ul | SAB | 100ul | 468 EUR |
![]() T7 tag Antibody |
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abx019171-100ug | Abbexa | 100 ug | 385.2 EUR |
![]() T7 tag Antibody |
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E300946 | EnoGene | 100ug | 275 EUR |
Description: Available in various conjugation types. |
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![]() Anti-Gasdermin D (N terminal) Antibody [PD00-18] |
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HA721144 | HUABIO | 100ul | 231 EUR |
Description: Gasdermin-D, N-terminal: Promotes pyroptosis in response to microbial infection and danger signals. Produced by the cleavage of gasdermin-D by inflammatory caspases CASP1 or CASP4 in response to canonical, as well as non-canonical (such as cytosolic LPS) inflammasome activators. After cleavage, moves to the plasma membrane where it strongly binds to inner leaflet lipids, including monophosphorylated phosphatidylinositols, such as phosphatidylinositol 4-phosphate, bisphosphorylated phosphatidylinositols, such as phosphatidylinositol (4,5)-bisphosphate, as well as phosphatidylinositol (3,4,5)-bisphosphate, and more weakly to phosphatidic acid and phosphatidylserine. Homooligomerizes within the membrane and forms pores of 10 - 15 nanometers (nm) of inner diameter, possibly allowing the release of mature IL1B and triggering pyroptosis . Exhibits bactericidal activity. Gasdermin-D, N-terminal released from pyroptotic cells into the extracellular milieu rapidly binds to and kills both Gram-negative and Gram-positive bacteria, without harming neighboring mammalian cells, as it does not disrupt the plasma membrane from the outside due to lipid-binding specificity. |
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![]() Parathyroid Hormone Antibody Cocktail / N + C Terminal |
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V2812-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: PTH is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody Cocktail / N + C Terminal |
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V2812-20UG | NSJ Bioreagents | 20 ug | 153.3 EUR |
Description: PTH is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody Cocktail / N + C Terminal |
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V2812IHC-7ML | NSJ Bioreagents | 7 ml | 349.3 EUR |
Description: PTH is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Parathyroid Hormone Antibody Cocktail / N + C Terminal |
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V2812SAF-100UG | NSJ Bioreagents | 100 ug | 349.3 EUR |
Description: PTH is a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. |
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![]() Perilipin (C terminal) antibody |
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20R-2599 | Fitzgerald | 100 uL | 685.2 EUR |
Description: Guinea Pig polyclonal Perilipin C terminal antibody |
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![]() Leptin amino terminal Antibody |
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abx023316-01ml | Abbexa | 0.1 ml | 1796.4 EUR |
![]() Leptin amino terminal Antibody |
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abx023317-01ml | Abbexa | 0.1 ml | 777.6 EUR |
![]() Adipophilin (C terminal) antibody |
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20R-2604 | Fitzgerald | 100 uL | 688.8 EUR |
Description: Guinea Pig polyclonal Adipophilin C terminal antibody |
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![]() Anti-T7 Tag Antibody |
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R1401-19 | HUABIO | 100ul | 189 EUR |
Description: The T7 tag is an epitope tag composed of an 11-residue peptide encoded from the leader sequence of the T7 bacteriophage gene10. This gene encodes a T7 major capsid protein whose function is not clear. The T7 tag has been used extensively as a general epitope tag in many expression vectors including the pET system that is based on T7 RNA polymerase expression systems. This antibody recognizes the T7-tag fused to either the amino- or carboxy-terminus of targeted proteins. |
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![]() Anti-T7 tag antibody |
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STJ140137 | St John's Laboratory | 150 µg | 489.6 EUR |
Description: Goat polyclonal antibody to T7 epitope tag. T7 epitope tag is useful for the labelling and detection of proteins by immunoprecipitation, immunostaining and immunoblotting techniques. Because of its small size, it is unlikely to affect the tagged protein's biochemical properties. |
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![]() PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175) Antibody |
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BNC941236-100 | Biotium | 100uL | 238.8 EUR |
Description: Primary antibody against PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175), CF594 conjugate, Concentration: 0.1mg/mL |
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![]() PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175) Antibody |
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BNC941236-500 | Biotium | 500uL | 652.8 EUR |
Description: Primary antibody against PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175), CF594 conjugate, Concentration: 0.1mg/mL |
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![]() PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175) Antibody |
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BNC801236-100 | Biotium | 100uL | 238.8 EUR |
Description: Primary antibody against PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175), CF680 conjugate, Concentration: 0.1mg/mL |
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![]() PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175) Antibody |
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BNC801236-500 | Biotium | 500uL | 652.8 EUR |
Description: Primary antibody against PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175), CF680 conjugate, Concentration: 0.1mg/mL |
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![]() PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175) Antibody |
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BNC811236-100 | Biotium | 100uL | 238.8 EUR |
Description: Primary antibody against PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175), CF680R conjugate, Concentration: 0.1mg/mL |
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![]() PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175) Antibody |
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BNC811236-500 | Biotium | 500uL | 652.8 EUR |
Description: Primary antibody against PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175), CF680R conjugate, Concentration: 0.1mg/mL |
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![]() PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175) Antibody |
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BNC701236-100 | Biotium | 100uL | 238.8 EUR |
Description: Primary antibody against PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175), CF770 conjugate, Concentration: 0.1mg/mL |
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![]() PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175) Antibody |
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BNC701236-500 | Biotium | 500uL | 652.8 EUR |
Description: Primary antibody against PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175), CF770 conjugate, Concentration: 0.1mg/mL |
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![]() PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175) Antibody |
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BNC881236-100 | Biotium | 100uL | 238.8 EUR |
Description: Primary antibody against PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175), CF488A conjugate, Concentration: 0.1mg/mL |
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![]() PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175) Antibody |
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BNC881236-500 | Biotium | 500uL | 652.8 EUR |
Description: Primary antibody against PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175), CF488A conjugate, Concentration: 0.1mg/mL |
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![]() PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175) Antibody |
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BNC051236-100 | Biotium | 100uL | 238.8 EUR |
Description: Primary antibody against PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175), CF405M conjugate, Concentration: 0.1mg/mL |
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![]() PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175) Antibody |
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BNC051236-500 | Biotium | 500uL | 652.8 EUR |
Description: Primary antibody against PTH (Parathyroid Hormone) (N & C Terminal) (3H9 + PTH/1175), CF405M conjugate, Concentration: 0.1mg/mL |