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Recombinant SOX9 抗体

SOX9 适用: 人 ELISA, Coat 宿主: 兔 Monoclonal SOX9-2287R unconjugated Recombinant Antibody
产品编号 ABIN6935478
发货至: 中国
  • 抗原 See all SOX9 抗体
    SOX9 (SRY (Sex Determining Region Y)-Box 9 (SOX9))
    抗体类型
    Recombinant Antibody
    适用
    • 135
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    • 5
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    宿主
    • 116
    • 20
    • 2
    克隆类型
    • 104
    • 34
    单克隆
    标记
    • 70
    • 9
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    This SOX9 antibody is un-conjugated
    应用范围
    • 109
    • 62
    • 43
    • 36
    • 31
    • 27
    • 27
    • 19
    • 9
    • 8
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    • 4
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    • 1
    ELISA, Coating (Coat)
    纯化方法
    Purified by Protein A/G
    免疫原
    Recombinant human full-length SOX9 protein
    克隆位点
    SOX9-2287R
    亚型
    IgG
    Top Product
    Discover our top product SOX9 Primary Antibody
  • 应用备注

    Positive Control: Human Skin Hair follicles.

    Known Application: ELISA (For coating use Ab at 1-5 μg/mL, order Ab without BSA), Optimal dilution for a specific application should be determined.

    限制
    仅限研究用
  • 浓度
    200 μg/mL
    缓冲液
    10 mM PBS with 0.05 % BSA & 0.05 % 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,-80 °C
    储存方法
    Antibody with azide - store at 2 to 8°C. Antibody without azide - store at -20 to -80°C. Antibody is stable for 24 months. Non-hazardous. No MSDS required.
    有效期
    24 months
  • 抗原
    SOX9 (SRY (Sex Determining Region Y)-Box 9 (SOX9))
    别名
    SOX9 (SOX9 产品)
    别名
    CMD1 antibody, CMPD1 antibody, SRA1 antibody, LOC100227849 antibody, 2010306G03Rik antibody, AV220920 antibody, mKIAA4243 antibody, SOX-9 antibody, cmd1 antibody, cmpd1 antibody, sox-9 antibody, sox9 antibody, sox9-a antibody, sox9-b antibody, sox9b antibody, sra1 antibody, SRY-box 9 antibody, transcription factor SOX-9 antibody, SRY (sex determining region Y)-box 9 antibody, SRY box 9 antibody, SRY-box 9 L homeolog antibody, SOX9 antibody, LOC100227849 antibody, Sox9 antibody, sox9.L antibody
    背景
    The specificity of this monoclonal antibody to its intended target was validated by HuProtTM Array, containing more than 19,000, full-length human proteins. Plays an important role in the normal skeletal development. May regulate the expression of other genes involved in chondrogenesis by acting as a transcription factor for these genes. Nucleus (Potential). Campomelic dysplasia (CMD1) [MIM:114290]: Rare, often lethal, dominantly inherited, congenital osteo-chondrodysplasia, associated with male-to-female autosomal sex reversal in two-thirds of the affected karyotypic males. A disease of the newborn characterized by congenital bowing and angulation of long bones, unusually small scapulae, deformed pelvis and spine and a missing pair of ribs. Craniofacial defects such as cleft palate, micrognathia, flat face and hypertelorism are common.
    分子量
    56kDa
    基因ID
    6662
    UniProt
    P48436
    途径
    EGFR Signaling Pathway, Stem Cell Maintenance, Regulation of Muscle Cell Differentiation, Tube Formation, Skeletal Muscle Fiber Development
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