SKU: WM1635 Categories: ,

Parathyroid Hormone [PTH] [PT0210] mouse mAb

Price range: $268.00 through $328.00

SKU: WM1635-50
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Product details

Background:
This gene encodes a member of the parathyroid family of proteins. The encoded preproprotein is proteolytically processed to generate a protein that binds to the parathyroid hormone/parathyroid hormone-related peptide receptor and regulates blood calcium and phosphate levels. Excess production of the encoded protein, known as hyperparathyroidism, can result in hypercalcemia and kidney stones. On the other hand, defective processing of the encoded protein may lead to hypoparathyroidism, which can result in hypocalcemia and numbness. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015],

Specifications

Size50μL/100μL
TargetParathyroid Hormone
ReactivityHuman
ApplicationsIHC, IF, ELISA
MW(Calculated)13kD
MW(Observed)
Host SpeciesMouse
IsotypeIgG1,Kappa
Conjugate/ModificationUnmodified
Recommended Dilution RatioIHC 1:200-400; IF 1:50-200; ELISA 1:500-5000 / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationPBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
PurificationThe antibody was affinity-purified from ascites by affinity-chromatography using specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
ClonalityMonoclonal
Clone NumberRMM0210
ImmunogenSynthesized peptide derived from human Parathyroid Hormone (PTH) AA range: 50-115
SpecificityThe antibody can specifically recognize human Parathyroid Hormone protein.
Gene NamePTH
Protein NameParathyroid hormone (PTH) (Parathormone) (Parathyrin)
Other Name
SpeciesHuman
Gene ID5741
UniprotP01270
Species.1
Gene ID.1
Uniprot.1
Species.2
Gene ID.2
Uniprot.2
Cellular LocalizationCytoplasmic, Membranous
Tissue Expression
Signaling_pathwayHuman Diseases >> Immune disease >> Rheumatoid arthritis
Research Areas>>Neuroactive ligand-receptor interaction; / >>Parathyroid hormone synthesis, secretion and action; / >>Endocrine and other factor-regulated calcium reabsorption; / >>Rheumatoid arthritis
FunctionDisease:Defects in PTH are a cause of familial isolated hypoparathyroidism (FIH) [MIM:146200]. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism.,Function:PTH elevates calcium level by dissolving the salts in bone and preventing their renal excretion.,online information:Parathyroid hormone entry,similarity:Belongs to the parathyroid hormone family.,
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