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HOXA13 抗体

HOXA13 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2460332
发货至: 中国
  • 抗原 See all HOXA13 抗体
    HOXA13 (Homeobox A13 (HOXA13))
    适用
    • 37
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    宿主
    • 37
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    克隆类型
    • 37
    • 1
    多克隆
    标记
    • 14
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    This HOXA13 antibody is un-conjugated
    应用范围
    • 37
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    • 3
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    Western Blotting (WB), ELISA
    纯化方法
    Antibody is purified by peptide affinity chromatography method.
    免疫原
    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human HOXA13.
    Top Product
    Discover our top product HOXA13 Primary Antibody
  • 应用备注
    HOXA13 antibody can be used for detection of HOXA13 by ELISA at 1:312500. HOXA13 antibody can be used for detection of HOXA13 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
    浓度
    1 mg/mL
    缓冲液
    Antibody is lyophilized in PBS buffer with 2 % sucrose.
    注意事项
    As with any antibody avoid repeat freeze-thaw cycles.
    储存条件
    4 °C/-20 °C
    储存方法
    For short periods of storage (days) store at 4 °C. For longer periods of storage, store HOXA13 antibody at -20 °C.
  • 抗原
    HOXA13 (Homeobox A13 (HOXA13))
    别名
    HOXA13 (HOXA13 产品)
    别名
    HOXA13 antibody, RGD1562483 antibody, HOX1 antibody, HOX1J antibody, Hd antibody, Hox-1.10 antibody, homeobox A13 antibody, homeo box A13 antibody, HOXA13 antibody, Hoxa13 antibody
    背景
    In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. Expansion of a polyalanine tract in the encoded protein can cause hand-foot-uterus syndrome, also known as hand-foot-genital syndrome. In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. Expansion of a polyalanine tract in the encoded protein can cause hand-foot-uterus syndrome, also known as hand-foot-genital syndrome. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
    分子量
    40 kDa
    基因ID
    3209
    NCBI登录号
    NP_000513
    UniProt
    P31271
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