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BEND2 抗体 (Biotin)

BEND2 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1403377
发货至: 中国
  • 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
    • 7
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This BEND2 antibody is conjugated to Biotin
    应用范围
    • 20
    • 13
    • 3
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (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
    Top Product
    Discover our top product BEND2 Primary Antibody
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    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 for 12 months.
    有效期
    12 months
  • 抗原
    BEND2 (BEN Domain Containing 2 (BEND2))
    别名
    BEND2 (BEND2 产品)
    别名
    CXorf20 antibody, BEN domain containing 2 antibody, BEND2 antibody
    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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