Parathyroid Hormone (PTH) (N- & C-Terminal) Antibody - Without BSA and Azide
Mouse Monoclonal Antibody [Clone 3H9 + PTH/1175 ]
|Application ||IHC, IF, FC|
|Other Accession||5741, 37045|
|Isotype||Mouse / IgG's|
|Clone Names||3H9 + PTH/1175|
|Other Names||Parathyroid hormone, PTH, Parathormone, Parathyrin, PTH|
|Storage||Store at 2 to 8°C.Antibody is stable for 24 months.|
|Precautions||Parathyroid Hormone (PTH) (N- & C-Terminal) Antibody - Without BSA and Azide is for research use only and not for use in diagnostic or therapeutic procedures.|
|Function||PTH elevates calcium level by dissolving the salts in bone and preventing their renal excretion. Stimulates [1-14C]-2- deoxy-D-glucose (2DG) transport and glycogen synthesis in osteoblastic cells.|
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Provided below are standard protocols that you may find useful for product applications.
Epitope of this MAb maps in the C-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.ĀIt 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.
Watson, P.H. and Hanley, D.A. 1993. Parathyroid hormone: regulation of synthesis and secretion. Clin. Invest. Med. 16: 58-77
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