PYGL Antibody
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货号:CSB-PA830394
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规格:¥1100
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图片:
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The image on the left is immunohistochemistry of paraffin-embedded Human thyroid cancer tissue using CSB-PA830394(PYGL Antibody) at dilution 1/35, on the right is treated with fusion protein. (Original magnification: ×200)
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The image on the left is immunohistochemistry of paraffin-embedded Human brain tissue using CSB-PA830394(PYGL Antibody) at dilution 1/35, on the right is treated with fusion protein. (Original magnification: ×200)
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Gel: 6%SDS-PAGE, Lysate: 40 μg, Lane 1-2: 231 cells, PC3 cells, Primary antibody: CSB-PA830394(PYGL Antibody) at dilution 1/400, Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution, Exposure time: 20 seconds
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其他:
产品详情
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Uniprot No.:P06737
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基因名:
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别名:Glycogen phosphorylase antibody; Glycogen phosphorylase L antibody; Glycogen phosphorylase liver antibody; Glycogen phosphorylase liver form antibody; GSD6 antibody; Hers disease; glycogen storage disease type VI antibody; liver form antibody; OTTHUMP00000233649 antibody; OTTHUMP00000233651 antibody; Phosphorylase glycogen liver antibody; Pygl antibody; PYGL_HUMAN antibody
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宿主:Rabbit
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反应种属:Human,Mouse,Rat
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免疫原:Fusion protein of Human PYGL
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
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抗体亚型:IgG
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纯化方式:Antigen affinity purification
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
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产品提供形式:Liquid
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应用范围:ELISA,WB,IHC
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推荐稀释比:
Application Recommended Dilution ELISA 1:2000-1:5000 WB 1:500-1:2000 IHC 1:30-1:150 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
相关产品
靶点详情
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功能:Allosteric enzyme that catalyzes the rate-limiting step in glycogen catabolism, the phosphorolytic cleavage of glycogen to produce glucose-1-phosphate, and plays a central role in maintaining cellular and organismal glucose homeostasis.
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基因功能参考文献:
- Susceptibility to excessive liver glycogen storage in patients with type 1 diabetes. PMID: 15223230
- Deficiency of liver glycogen phosphorylase is predominantly the result of missense mutations affecting enzyme activity. There are no common mutations and the severity of clinical symptoms varies significantly. PMID: 17705025
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相关疾病:Glycogen storage disease 6 (GSD6)
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亚细胞定位:Cytoplasm, cytosol.
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蛋白家族:Glycogen phosphorylase family
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数据库链接:
HGNC: 9725
OMIM: 232700
KEGG: hsa:5836
STRING: 9606.ENSP00000216392
UniGene: Hs.282417
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