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>   home   >   Products   >   Primary Antibodies   >   Signal Transduction   >    Parathyroid Hormone (PTH) (N-Terminal) Antibody - With BSA and Azide   

Parathyroid Hormone (PTH) (N-Terminal) Antibody - With BSA and Azide

Mouse Monoclonal Antibody [Clone 3H9 ]

  • IHC -  Parathyroid Hormone (PTH) (N-Terminal) Antibody - With BSA and Azide AH12143
    Formalin-fixed, paraffin-embedded human Parathyroid stained with PTH Monoclonal Antibody (3H9).
Product Information
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Primary Accession P01270
Other Accession 5741, 37045
Reactivity Human, Mouse, Rat, Rabbit, Pig, Cow, Dog
Host Mouse
Clonality Monoclonal
Isotype Mouse / IgG2b, kappa
Clone Names 3H9
Calculated MW 9kDa
Additional Information
Gene ID 5741
Other Names Parathyroid hormone, PTH, Parathormone, Parathyrin, PTH
StorageStore at 2 to 8°C.Antibody is stable for 24 months.
Precautions Parathyroid Hormone (PTH) (N-Terminal) Antibody - With BSA and Azide is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name PTH
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.
Cellular Location Secreted.
Research Areas
Citations (0)

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Epitope of this MAb maps in between aa 1-34. 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.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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$ 124.00
$ 324.00
$ 454.00
Cat# AH12143
(40 western blots)
Availability: 2-3 days
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