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SOX3 抗体

The 兔 多克隆 anti-SOX3 antibody (ABIN7231462) specifically detects SOX3 in WB 和 ELISA. The antibody is reactive with 人 和 小鼠 samples.
产品编号 ABIN7231462
发货至: 中国
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Quick Overview for SOX3 抗体 (ABIN7231462)

抗原

See all SOX3 抗体
SOX3 (SRY (Sex Determining Region Y)-Box 3 (SOX3))

适用

  • 39
  • 20
  • 6
  • 6
  • 5
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
人, 小鼠

宿主

  • 39
  • 1
  • 1

克隆类型

  • 40
  • 1
多克隆

标记

  • 25
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SOX3 antibody is un-conjugated

应用范围

  • 29
  • 21
  • 5
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • 原理

    Rabbit Anti-SOX3 Polyclonal Antibody

    特异性

    The antibody detects endogenous levels of SOX3 protein

    纯化方法

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    免疫原

    Synthesized peptide derived from part region of human SOX3 protein

    亚型

    IgG
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

    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

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

    有效期

    12 months
  • 抗原

    SOX3 (SRY (Sex Determining Region Y)-Box 3 (SOX3))

    别名

    SOX3

    背景

    Transcription factor SOX-3SOX3 encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. SRY-Box 3 may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene have been associated with X-linked cognitive disability with growth hormone deficiency.

    分子量

    49kD

    基因ID

    6658

    UniProt

    P41225
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