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ASXL1 抗体 (AA 521-549)

This anti-ASXL1 antibody is a 兔 多克隆 antibody detecting ASXL1 in WB, FACS, IF 和 IHC (p). Suitable for 小鼠.
产品编号 ABIN655084
发货至: 中国

Quick Overview for ASXL1 抗体 (AA 521-549) (ABIN655084)

抗原

See all ASXL1 抗体
ASXL1 (Additional Sex Combs Like 1 (ASXL1))

适用

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  • 1
小鼠

宿主

  • 26
  • 3

克隆类型

  • 26
  • 3
多克隆

标记

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This ASXL1 antibody is un-conjugated

应用范围

  • 19
  • 13
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  • 10
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Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

克隆位点

RB24070
  • 抗原表位

    • 8
    • 3
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    AA 521-549

    纯化方法

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    免疫原

    This ASXL1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 521-549 amino acids from the Central region of human ASXL1.

    亚型

    Ig Fraction
  • 应用备注

    IF: 1:10~50. WB: 1:1000. IHC-P: 1:50~100. FC: 1:10~50

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    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

    4 °C,-20 °C

    储存方法

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    有效期

    6 months
  • 抗原

    ASXL1 (Additional Sex Combs Like 1 (ASXL1))

    别名

    ASXL1

    背景

    This gene is similar to the Drosophila additional sex combs gene, which encodes a chromatin-binding protein required for normal determination of segment identity in the developing embryo. The protein is a member of the Polycomb group of proteins, which are necessary for the maintenance of stable repression of homeotic and other loci. The protein is thought to disrupt chromatin in localized areas, enhancing transcription of certain genes while repressing the transcription of other genes. The protein encoded by this gene functions as a ligand-dependent co-activator for retinoic acid receptor in cooperation with nuclear receptor coactivator 1. Mutations in this gene are associated with myelodysplastic syndromes and chronic myelomonocytic leukemia. Alternative splicing results in multiple transcript variants.

    分子量

    165432

    基因ID

    171023

    NCBI登录号

    NP_056153

    UniProt

    Q8IXJ9

    途径

    Retinoic Acid Receptor Signaling Pathway
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