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ATRX 抗体

This 小鼠 单克隆 antibody specifically detects ATRX in ELISA. It exhibits reactivity toward 人.
产品编号 ABIN7880993
发货至: 中国
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Quick Overview for ATRX 抗体 (ABIN7880993)

抗原

See all ATRX 抗体
ATRX (helicase 2, X-linked (ATRX))

适用

  • 86
  • 20
  • 6
  • 3
  • 2
  • 2

宿主

  • 50
  • 38
  • 1
小鼠

克隆类型

  • 54
  • 35
单克隆

标记

  • 54
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ATRX antibody is un-conjugated

应用范围

  • 35
  • 32
  • 26
  • 21
  • 14
  • 13
  • 9
  • 9
  • 4
  • 3
  • 1
  • 1
  • 1
ELISA

克隆位点

23c
  • 原理

    ATRX Antibody / RAD54

    纯化方法

    Protein G affinity chromatography

    免疫原

    Recombinant human ATRX protein was used as the immunogen for this ATRX antibody.

    亚型

    IgG1, kappa
  • 应用备注

    The concentration stated for each application is a general starting point. Variations in protocols, secondaries and substrates may require the ATRX antibody to be titered up or down for optimal performance.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.2 mg/mL

    缓冲液

    0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced) and 0.05 % 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

    Store the ATRX antibody at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).
  • 抗原

    ATRX (helicase 2, X-linked (ATRX))

    别名

    ATRX

    背景

    ATRX is a member of the Snf2 family of helicase/ATPases, which contribute to the remodeling of the nucelosome structure in an ATP-dependent manner, and facilitate the initiation of transcription and replication. Structurally, it contains a PHD zinc finger motif. ATRX is regulated throughout the cell cycle where it is differentially distributed within the nucleus. During interphase, it predominately associates with the nuclear matrix, while during mitosis, ATRX localizes with condensed chromatin. At the onset of M phase, phosphorylation rapidly induces this redistribution of ATRX to the short arms of human acrocentric chromosomes, where it then specifically complexes with heterochromatin protein 1 i± to mediate chromosomal segregation. Mutations in the gene correlate with a high incidence of severe X-linked form of syndromal mental retardation associated with alpha-thalassemia or ATRX syndrome.

    UniProt

    P46100
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