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PHKG2 抗体 (AA 237-406)

This anti-PHKG2 antibody is a 兔 多克隆 antibody detecting PHKG2 in WB 和 IF. Suitable for 人.
产品编号 ABIN6145563
发货至: 中国

Quick Overview for PHKG2 抗体 (AA 237-406) (ABIN6145563)

抗原

See all PHKG2 抗体
PHKG2 (phosphorylase Kinase, gamma 2 (Testis) (PHKG2))

适用

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宿主

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克隆类型

  • 53
  • 5
多克隆

标记

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This PHKG2 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunofluorescence (IF)
  • 抗原表位

    • 15
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    AA 237-406

    序列

    RQILMLRMIM EGQYQFSSPE WDDRSSTVKD LISRLLQVDP EARLTAEQAL QHPFFERCEG SQPWNLTPRQ RFRVAVWTVL AAGRVALSTH RVRPLTKNAL LRDPYALRSV RHLIDNCAFR LYGHWVKKGE QQNRAALFQH RPPGPFPIMG PEEEGDSAAI TEDEAVLVLG

    交叉反应

    人, 小鼠, 大鼠

    产品特性

    Polyclonal Antibodies

    免疫原

    Recombinant fusion protein containing a sequence corresponding to amino acids 237-406 of human PHKG2 (NP_000285.1).

    亚型

    IgG
  • 应用备注

    WB,1:500 - 1:2000,IF,1:50 - 1:200

    说明

    HIGH QUALITY

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    PBS with 0.02 % sodium azide,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.

    储存条件

    -20 °C

    储存方法

    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原

    PHKG2 (phosphorylase Kinase, gamma 2 (Testis) (PHKG2))

    别名

    PHKG2

    背景

    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.,PHKG2,GSD9C,Cancer,Signal Transduction,Kinase,Endocrine & Metabolism,Carbohydrate metabolism,PHKG2

    分子量

    43 kDa/46 kDa

    基因ID

    5261

    UniProt

    P15735

    途径

    Cellular Glucan Metabolic Process, Regulation of Carbohydrate Metabolic Process
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