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SHOX2 抗体

SHOX2 适用: 人, 大鼠, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7264337
发货至: 中国
  • 抗原 See all SHOX2 抗体
    SHOX2 (Short Stature Homeobox 2 (SHOX2))
    适用
    • 17
    • 9
    • 7
    • 5
    • 5
    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    人, 大鼠, 小鼠
    宿主
    • 10
    • 7
    克隆类型
    • 13
    • 4
    多克隆
    标记
    • 17
    This SHOX2 antibody is un-conjugated
    应用范围
    • 14
    • 8
    • 2
    • 1
    • 1
    Western Blotting (WB)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human SHOX2 (NP_003021.3).
    亚型
    IgG
    Top Product
    Discover our top product SHOX2 Primary Antibody
  • 应用备注
    WB 1:500-1:2000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    SHOX2 (Short Stature Homeobox 2 (SHOX2))
    别名
    SHOX2 (SHOX2 产品)
    别名
    SHOX2 antibody, og12 antibody, shot antibody, og12x antibody, ogi2x antibody, OG12 antibody, OG12X antibody, SHOT antibody, 6330543G17Rik antibody, Og12x antibody, Prx3 antibody, zgc:65884 antibody, zgc:77344 antibody, short stature homeobox 2 antibody, SHOX2 antibody, shox2 antibody, Shox2 antibody
    背景
    This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants.
    分子量

    Observed_MW: 30 kDa

    Calculated_MW: 33 kDa/34 kDa/37 kDa

    基因ID
    6474
    UniProt
    O60902
    途径
    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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