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TBL1X 抗体 (AA 100-200)

This anti-TBL1X antibody is a 兔 多克隆 antibody detecting TBL1X in WB. Suitable for 人.
产品编号 ABIN7270901
发货至: 中国

Quick Overview for TBL1X 抗体 (AA 100-200) (ABIN7270901)

抗原

See all TBL1X 抗体
TBL1X (Transducin (Beta)-Like 1X-Linked (TBL1X))

适用

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宿主

  • 18
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  • 1

克隆类型

  • 20
  • 2
多克隆

标记

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  • 1
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  • 1
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This TBL1X antibody is un-conjugated

应用范围

  • 11
  • 10
  • 3
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Western Blotting (WB)
  • 抗原表位

    • 6
    • 3
    • 2
    • 1
    • 1
    AA 100-200

    原理

    TBL1X Rabbit pAb

    序列

    LISILQKGLQ YVEAEISINE DGTVFDGRPI ESLSLIDAVM PDVVQTRQQA FREKLAQQQA SAAAAAAAAT AAATAATTTS AGVSHQNPSK NREATVNGEE N

    交叉反应

    人, 小鼠, 大鼠

    产品特性

    Polyclonal Antibodies

    纯化方法

    Affinity purification

    免疫原

    A synthetic peptide corresponding to a sequence within amino acids 100-200 of human TBL1X (NP_005638.1).

    亚型

    IgG
  • 应用备注

    WB,1:500 - 1:2000

    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

    TBL1X (Transducin (Beta)-Like 1X-Linked (TBL1X))

    别名

    TBL1X

    背景

    The protein encoded by this gene has sequence similarity with members of the WD40 repeat-containing protein family. The WD40 group is a large family of proteins, which appear to have a regulatory function. It is believed that the WD40 repeats mediate protein-protein interactions and members of the family are involved in signal transduction, RNA processing, gene regulation, vesicular trafficking, cytoskeletal assembly and may play a role in the control of cytotypic differentiation. This encoded protein is found as a subunit in corepressor SMRT (silencing mediator for retinoid and thyroid receptors) complex along with histone deacetylase 3 protein. This gene is located adjacent to the ocular albinism gene and it is thought to be involved in the pathogenesis of the ocular albinism with late-onset sensorineural deafness phenotype. Four transcript variants encoding two different isoforms have been found for this gene. This gene is highly similar to the Y chromosome TBL1Y gene.,TBL1X,EBI,SMAP55,TBL1,Epigenetics & Nuclear Signaling,Nuclear Receptor Signaling,Cancer,Endocrine & Metabolism,Lipid Metabolism,Endocrine and metabolic diseases,Diabetes,Metabolic disorders,Obesity,Neuroscience,TBL1X

    分子量

    57kDa/62kDa

    基因ID

    6907

    UniProt

    O60907

    途径

    Sensory Perception of Sound, Regulation of Lipid Metabolism by PPARalpha
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