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BEND2 抗体 (AbBy Fluor® 555)

This anti-BEND2 antibody is a 兔 多克隆 antibody detecting BEND2 in WB 和 IF (p). Suitable for 人.
产品编号 ABIN1403375
发货至: 中国
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Room 801-803
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Quick Overview for BEND2 抗体 (AbBy Fluor® 555) (ABIN1403375)

抗原

See all BEND2 抗体
BEND2 (BEN Domain Containing 2 (BEND2))

适用

  • 20
  • 1

宿主

  • 18
  • 2

克隆类型

  • 20
多克隆

标记

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This BEND2 antibody is conjugated to AbBy Fluor® 555

应用范围

  • 20
  • 12
  • 4
  • 1
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 交叉反应

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human BEND2/CXorf56

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    BEND2 (BEN Domain Containing 2 (BEND2))

    别名

    BEND2

    背景

    Synonyms: BEN domain-containing protein 2, BEN domain containing 2, BEND 2, BEND2, BEND-2, Chromosome X open reading frame 20, MGC33653, BEND2_HUMAN, CXorf56.

    Background: BEND2 is a 799 amino acid protein that contains two BEN domains. BEND2 exists as two alternatively spliced isoforms and is considered a complete proteome. BEN domain mediates proteinDNA and proteinprotein interactions during chromatin organization and transcription. BEN domain may play a role in organization of viral DNA during replication or transcription. The BEND2 gene maps to human chromosome Xp22.13. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The X and Y chromosomes are the human sex chromosomes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.

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