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Merck
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主要文件

SAB1300187

Sigma-Aldrich

Anti-PYGM (C-term) antibody produced in rabbit

Ig fraction of antiserum, buffered aqueous solution

别名:

Anti-Glycogen phosphorylase, Anti-Muscle form, Anti-Myophosphorylase, Anti-PYGM

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About This Item

分類程式碼代碼:
12352203
NACRES:
NA.41

生物源

rabbit

品質等級

共軛

unconjugated

抗體表格

Ig fraction of antiserum

抗體產品種類

primary antibodies

無性繁殖

polyclonal

形狀

buffered aqueous solution

物種活性

human

技術

indirect ELISA: 1:1000
western blot: 1:100-1:500

NCBI登錄號

UniProt登錄號

運輸包裝

dry ice

儲存溫度

−20°C

目標翻譯後修改

unmodified

基因資訊

human ... PYGM(5837)

一般說明

Glycogen phosphorylase, muscle associated (PYGM) encodes glycogen phosphorylase or myophosphorylase. In human chromosome, the gene PYGM is localized on 11q13.1.

免疫原

PYGM (NP_005600, 703-737)
This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the C-terminal region of human PYGM.

生化/生理作用

PYGM catalyses and regulates the breakdown of glycogen to glucose-1-phosphate. Defects in PYGM are the cause of Glycogenosis type V/ glycogen storage disease type 5 (GSD5), also known as McArdle disease/ myophosphorylase deficiency, is an autosomal recessive disorder. GSD5 is a metabolic disorder resulting in myopathy characterized by exercise intolerance, cramps, muscle weakness and recurrent myoglobinuria.

外觀

Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide.

免責聲明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

nwg

閃點(°F)

Not applicable

閃點(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Analysis of loss of heterozygosity on chromosome 11 and infrequent inactivation of the MEN1 gene in sporadic pituitary adenomas
Tanaka C, et al.
The Journal of Clinical Endocrinology and Metabolism, 83(8), 2631-2634 (1998)
Glycogen storage diseases: diagnosis, treatment and outcome
Chen MA and Weinstein DA
Translational Science of Rare Diseases, 1(1), 45-72 (2016)
Knock-in mice for the R50X mutation in the PYGM gene present with McArdle disease
Nogales-Gadea G, et al.
Brain, 135(7), 2048-2057 (2012)

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