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Short Stature Homeobox 2 (SHOX2) (N-Term) Peptide

SHOX2 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN983719
发货至: 中国
  • 抗原 See all SHOX2 products
    SHOX2 (Short Stature Homeobox 2 (SHOX2))
    蛋白结构域
    N-Term
    宿主
    资源
    • 2
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB)
    产品特性
    This is a synthetic peptide designed for use in combination with anti-SHOX2 antibody (Catalog #: ARP33285_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    纯化方法
    Purified
  • 应用备注
    Each Investigator should determine their own optimal working dilution for specific applications.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    浓度
    1 mg/mL
    缓冲液
    Final peptide concentration is 1 mg/mL in PBS.
    注意事项
    Avoid repeated freeze-thaw cycles.
    储存条件
    -20 °C
    储存方法
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • 抗原
    SHOX2 (Short Stature Homeobox 2 (SHOX2))
    别名
    SHOX2 Peptide, og12 Peptide, shot Peptide, og12x Peptide, ogi2x Peptide, OG12 Peptide, OG12X Peptide, SHOT Peptide, 6330543G17Rik Peptide, Og12x Peptide, Prx3 Peptide, zgc:65884 Peptide, zgc:77344 Peptide, short stature homeobox 2 Peptide, SHOX2 Peptide, shox2 Peptide, Shox2 Peptide
    背景
    SHOX2 is a member of the homeo box family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeo box 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 homeo box genes. SHOX is a pseudoautosomal homeo box gene that is thought to be responsible for idiopathic short stature and implicated to play a role in the short stature phenotype of Turner syndrome patients. This gene is a member of the homeo box family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeo box 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 homeo box genes. SHOX is a pseudoautosomal homeo box gene that is thought to be responsible for idiopathic short stature and implicated to play a role 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 has been observed at this locus and two variants, each encoding a distinct isoform, have been identified.

    Alias Symbols: OG12, OG12X, OGI2X, SHOT

    Protein Size: 331
    分子量
    35 kDa
    基因ID
    6474
    NCBI登录号
    NM_006884, NP_006875
    UniProt
    O60902
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