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SATB2 抗体 (AA 377-499)

SATB2 适用: 人 ELISA, IHC, FACS 宿主: 小鼠 Monoclonal 7B2E11 unconjugated
产品编号 ABIN7193354
发货至: 中国
  • 抗原 See all SATB2 抗体
    SATB2 (SATB Homeobox 2 (SATB2))
    抗原表位
    • 16
    • 8
    • 7
    • 7
    • 6
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 377-499
    适用
    • 64
    • 34
    • 29
    • 1
    • 1
    • 1
    • 1
    宿主
    • 57
    • 7
    小鼠
    克隆类型
    • 46
    • 18
    单克隆
    标记
    • 29
    • 5
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This SATB2 antibody is un-conjugated
    应用范围
    • 46
    • 22
    • 15
    • 14
    • 14
    • 8
    • 8
    • 7
    • 5
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS)
    原理
    SATB2 Antibody
    纯化方法
    Purified antibody
    免疫原
    Purified recombinant fragment of human SATB2 (AA: 377-499) expressed in E. Coli.
    克隆位点
    7B2E11
    亚型
    IgG1
    Top Product
    Discover our top product SATB2 Primary Antibody
  • 应用备注

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Purified antibody in PBS with 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 at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • 抗原
    SATB2 (SATB Homeobox 2 (SATB2))
    别名
    SATB2 (SATB2 产品)
    别名
    RGD1562369 antibody, mKIAA1034 antibody, SATB homeobox 2 antibody, special AT-rich sequence binding protein 2 antibody, SATB2 antibody, satb2 antibody, Satb2 antibody
    背景

    Description:

    This gene encodes a DNA binding protein that specifically binds nuclear matrix attachment regions. The encoded protein is involved in transcription regulation and chromatin remodeling. Defects in this gene are associated with isolated cleft palate and cognitive disability. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Feb 2010]

    Aliases: GLSS

    分子量
    82.6kDa
    基因ID
    23314
    UniProt
    Q9UPW6
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