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SOX9 抗体 (AA 351-450) (FITC)

This FITC-conjugated 兔 多克隆 anti-SOX9 antibody specifically detects SOX9 in WB, FACS, IF (cc) 和 IF (p). The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN6945020
发货至: 中国
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Quick Overview for SOX9 抗体 (AA 351-450) (FITC) (ABIN6945020)

抗原

See all SOX9 抗体
SOX9 (SRY (Sex Determining Region Y)-Box 9 (SOX9))

适用

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人, 小鼠, 大鼠

宿主

  • 133
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克隆类型

  • 98
  • 89
多克隆

标记

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This SOX9 antibody is conjugated to FITC

应用范围

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Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

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    AA 351-450

    交叉反应

    人, 小鼠, 大鼠

    预测反应

    Pig,Horse,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human SOX9

    亚型

    IgG
  • 应用备注

    FCM 1:20-100
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    SOX9 (SRY (Sex Determining Region Y)-Box 9 (SOX9))

    别名

    SOX9

    背景

    Synonyms: CMD 1, CMD1, CMPD 1, CMPD1, SOX 9, Sox9, SOX9_HUMAN, SRA 1, SRA1 antibody SRY (sex determining region Y) box 9 (campomelic dysplasia autosomal, SRY (sex determining region Y) box 9, SRY (sex determining region Y)-box 9, SRY (sex-determining region Y)-box 9 protein, Transcription factor SOX 9, Transcription factor SOX-9, transcription factor SOX9, campomelic dysplasia autosomal sex reversal.

    Background: The protein encoded by this gene recognizes the sequence CCTTGAG along with other members of the HMG-box class DNA-binding proteins. It acts during chondrocyte differentiation and, with steroidogenic factor 1, regulates transcription of the anti-Muellerian hormone (AMH) gene. Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia, frequently with sex reversal. [provided by RefSeq].

    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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