PHKG2 抗体
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- 抗原 See all PHKG2 抗体
- PHKG2 (phosphorylase Kinase, gamma 2 (Testis) (PHKG2))
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适用
- 人, 小鼠, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This PHKG2 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)
- 免疫原
- phosphorylase kinase, gamma 2 (testis)
- 亚型
- IgG
- Top Product
- Discover our top product PHKG2 Primary Antibody
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- 应用备注
- Optimal working dilution should be determined by the investigator.
- 说明
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mouse testis tissue were subjected to SDS PAGE followed by western blot with FNab06395(PHKG2 antibody) at dilution of 1:300
- 限制
- 仅限研究用
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- 缓冲液
- PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 注意事项
- Avoid repeated freeze / thaw cycles.
- 储存条件
- -20 °C
- 有效期
- 12 months
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- 抗原
- PHKG2 (phosphorylase Kinase, gamma 2 (Testis) (PHKG2))
- 别名
- PHKG2 (PHKG2 产品)
- 别名
- PHKG2 antibody, MGC145608 antibody, zgc:55863 antibody, GSD9C antibody, 1500017I02Rik antibody, phosphorylase kinase catalytic subunit gamma 2 antibody, phosphorylase kinase, gamma 2 (testis) antibody, phosphorylase kinase, gamma 2 (testis) L homeolog antibody, PHKG2 antibody, phkg2 antibody, phkg2.L antibody, Phkg2 antibody
- 背景
- Synonyms: Background:Phosphorylase kinase is a polymer of 16 subunits, four each of alpha, beta, gamma and delta. The alpha subunit includes the skeletal muscle and hepatic isoforms, encoded by two different genes. The beta subunit is the same in both the muscle and hepatic isoforms, and encoded by one gene. The gamma subunit also includes the skeletal muscle and hepatic isoforms, and the hepatic isoform is encoded by this gene. The delta subunit is a calmodulin and can be encoded by three different genes. The gamma subunits contain the active site of the enzyme, whereas the alpha and beta subunits have regulatory functions controlled by phosphorylation. The delta subunit mediates the dependence of the enzyme on calcium concentration. Mutations in this gene cause glycogen storage disease type 9C, also known as autosomal liver glycogenosis. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.
- 基因ID
- 5261
- UniProt
- P15735
- 途径
- Cellular Glucan Metabolic Process, Regulation of Carbohydrate Metabolic Process
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