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BZW2 抗体 (FITC)

BZW2 适用: 人, 小鼠, 大鼠 WB, IF (p) 宿主: 兔 Polyclonal FITC
产品编号 ABIN1400240
发货至: 中国
  • 抗原 See all BZW2 抗体
    BZW2 (Basic Leucine Zipper and W2 Domains 2 (BZW2))
    适用
    • 31
    • 18
    • 17
    • 2
    • 2
    • 2
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    • 1
    人, 小鼠, 大鼠
    宿主
    • 29
    • 2
    克隆类型
    • 31
    多克隆
    标记
    • 12
    • 1
    • 1
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    • 1
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    This BZW2 antibody is conjugated to FITC
    应用范围
    • 24
    • 12
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    交叉反应
    人, 小鼠, 大鼠
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human BZW2
    亚型
    IgG
    Top Product
    Discover our top product BZW2 Primary Antibody
  • 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
    BZW2 (Basic Leucine Zipper and W2 Domains 2 (BZW2))
    别名
    BZW2 (BZW2 产品)
    别名
    HSPC028 antibody, MGC84347 antibody, MST017 antibody, MSTP017 antibody, 1110001I24Rik antibody, Bdm2 antibody, Hfb2 antibody, zgc:55580 antibody, basic leucine zipper and W2 domains 2 antibody, basic leucine zipper and W2 domains 2 L homeolog antibody, BZW2 antibody, bzw2.L antibody, Bzw2 antibody, bzw2 antibody
    背景

    Synonyms: HSPC028, MSTP017 antibody Basic leucine zipper and W2 domain containing protein 2, Basic leucine zipper and W2 domains 2, BZW 2, MST017, BZW2_HUMAN.

    Background: BZW2, also known as HSPC028 or MSTP017, is a 419 amino acid protein that contains one W2 domain and is thought to be involved in neuronal differentiation. The gene encoding BZW2 maps to human chromosome 7. Chromosome 7 houses over 1,000 genes and comprises nearly 5 % of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders, including cases of acute myelogenous leukemia and myelodysplasia.

    基因ID
    28969
    途径
    SARS-CoV-2 Protein Interactome
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