PTH Polyclonal Antibody

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商品货号： PLA017766

适应性： 人,大鼠,小鼠,

￥600元

规格：

40μL 100μL 200μL

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说明书

商品描述

基因名称： PTH
蛋白名称： Parathyroid hormone
Human_gene_id： 5741
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5741
Human_swiss_prot_no： P01270
Human_swiss_link： http://www.uniprot.org/uniprotkb/P01270/entry
特异性： PTH Polyclonal Antibody detects endogenous levels of PTH protein.
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： WB 1:500-2000;IHC-p 1:50-300
纯化工艺： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度： 1 mg/ml
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
其他名称： PTH; Parathyroid hormone; PTH; Parathormone; Parathyrin
实测条带： 16kD
功能： disease: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.,
相关产品： YT3897,YM6471,YM6470,KA3352C
细胞定位： Secreted.
科研货号： PLA017766

PTH Polyclonal Antibody

Catalog No PLA017766

Product information

基因名称： PTH
蛋白名称： Parathyroid hormone
Human_gene_id： 5741
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5741
Human_swiss_prot_no： P01270
Human_swiss_link： http://www.uniprot.org/uniprotkb/P01270/entry
特异性： PTH Polyclonal Antibody detects endogenous levels of PTH protein.
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： WB 1:500-2000;IHC-p 1:50-300
纯化工艺： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度： 1 mg/ml
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
其他名称： PTH; Parathyroid hormone; PTH; Parathormone; Parathyrin
实测条带： 16kD
功能： disease: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.,
相关产品： YT3897,YM6471,YM6470,KA3352C
细胞定位： Secreted.
科研货号： PLA017766

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