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- Home > Products > Ab Pairs/Kits > Ab Pairs for IP-WB > Plasma/Serum > PYGL (Human) IP-WB Antibody Pair
PYGL (Human) IP-WB Antibody Pair
- 目录号 # : H00005836-PW1
- 访问频率 :
- 尺寸
- 价格
- 库存
- 可得性
- 购物车
- 1 Set
- USD $ 589
- order now, ship in 3 days
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- Specification
- Product Description:
- This IP-WB antibody pair set comes with one antibody for immunoprecipitation and another to detect the precipitated protein in western blot.
- Reactivity:
- Human
- Quality Control Testing:
- Immunoprecipitation-Western Blot (IP-WB)
Immunoprecipitation of PYGL transfected lysate using rabbit polyclonal anti-PYGL and Protein A Magnetic Bead (U0007), and immunoblotted with rabbit polyclonal anti-PYGL.
- Supplied Product:
- Antibody pair set content:
1. Antibody pair for IP: rabbit polyclonal anti-PYGL (300 ul)
2. Antibody pair for WB: rabbit polyclonal anti-PYGL (50 ul)
- Storage Instruction:
- Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.
- MSDS:
Download
- Applications
- Immunoprecipitation-Western Blot
- Protocol Download
- Application Image
- Immunoprecipitation-Western Blot
- Entrez GeneID:
- 5836
- Gene Name:
- PYGL
- Gene Alias:
- GSD6
- Gene Description:
- phosphorylase, glycogen, liver
- Omim ID:
- 232700
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes a homodimeric protein that catalyses the cleavage of alpha-1,4-glucosidic bonds to release glucose-1-phosphate from liver glycogen stores. This protein switches from inactive phosphorylase B to active phosphorylase A by phosphorylation of serine residue 15. Activity of this enzyme is further regulated by multiple allosteric effectors and hormonal controls. Humans have three glycogen phosphorylase isozymes that are primarily expressed in liver, brain and muscle, respectively. The liver isozyme serves the glycemic demands of the body in general while the brain and muscle isozymes supply just those tissues. In glycogen storage disease type VI, or Hers disease, mutations in liver glycogen phosphorylase inhibit the conversion of glycogen to glucose and results in moderate hypoglycemia, mild ketosis, growth retardation and hepatomegaly. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq
- Other Designations:
- Hers disease,glycogen phosphorylase, liver,glycogen storage disease type VI,phosphorylase, glycogen; liver (Hers disease, glycogen storage disease type VI)
- Related Disease
