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SATB2 抗体 (AA 410-439)

SATB2 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN3032518
发货至: 中国
  • 抗原 See all SATB2 抗体
    SATB2 (SATB Homeobox 2 (SATB2))
    抗原表位
    • 16
    • 7
    • 7
    • 7
    • 6
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 410-439
    适用
    • 67
    • 35
    • 29
    • 1
    • 1
    • 1
    • 1
    宿主
    • 58
    • 9
    克隆类型
    • 45
    • 22
    多克隆
    标记
    • 32
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This SATB2 antibody is un-conjugated
    应用范围
    • 49
    • 22
    • 16
    • 14
    • 14
    • 11
    • 8
    • 8
    • 7
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA
    交叉反应 (详细)
    Expected species reactivity: Mouse
    纯化方法
    Antigen affinity purified
    免疫原
    A portion of amino acids 410-439 from the human protein was used as the immunogen for this SATB2 antibody.
    亚型
    Ig Fraction
    Top Product
    Discover our top product SATB2 Primary Antibody
  • 应用备注
    Titration of the SATB2 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    In 1X PBS, pH 7.4, with 0.09 % 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
    -20 °C
    储存方法
    Aliquot the SATB2 antibody and store frozen at -20°C or colder. Avoid repeated 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
    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 mental retardation. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq].
    UniProt
    Q9UPW6
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