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位置: 首页> 品牌> Sigma-Aldrich> 抗-SOX9 兔抗

Anti-SOX9 antibody produced in rabbit

抗-SOX9 兔抗

品牌
Sigma-Aldrich
货号
AV37986
规格纯度
affinity isolated antibody
价格
6305.78 *本价格含增值税费
促销
服务
  • 原厂保证
  • 包邮
  • 增值税票
数量
- +
半岛bd体育手机客户端 名称:
Anti-SOX9 antibody produced in rabbit
Anti-SRY (sex determining region Y)-box 9 (campomelic dysplasia, autosomal sex-reversal)
Anti-CMD1
Anti-CMPD1
Anti-SRA1
抗-SOX9 兔抗
半岛bd体育手机客户端 介绍:

半岛bd体育手机客户端 说明

一般描述

SRγ (sex determining region γ) (SOX) are HMG box containing transcription factors that bind to the minor groove of DNA. Sox proteins family members regulate a variety of aspects of development. SRγ (sex determining region γ)-box 9 (SOX9, CMD1, CMPD1, SRA1, SRγ) is a master regulator of chondrocyte differentiation and chondrogenesis, which results in the formation of cartilage.

特异性

Anti-SOX9 polyclonal antibody reacts with human, mouse, rat, canine, chicken, and pig SRγ (sex determining region γ)-box 9 proteins.

免疫原

Synthetic peptide directed towards the C terminal region of human SOX9

应用

Anti-SOX9 polyclonal antibody is used to tag SRγ (sex determining region γ)-box 9 for detection and quantitation by Western blotting and in plasma by immunohistochemical (IHC) techniques. It is used as a probe to determine the roles of SRγ (sex determining region γ)-box 9 in chondrocyte differentiation and cartilage formation.

生化/生理作用

SOX9 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.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. 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.

序列

Synthetic peptide located within the following region: AGQGTGLYSTFTYMNPAQRPMYTPIADTSGVPSIPQTHSPQHWEQPVYTQ

外形

Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.

免责声明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

半岛bd体育手机客户端 性质

生物来源 rabbit
质量水平 100
偶联物 unconjugated
抗体形式 affinity isolated antibody
antibody product type primary antibodies
克隆 polyclonal
形式 buffered aqueous solution
分子量 56 kDa
species reactivity rat, horse, human, pig, dog, mouse, rabbit
浓度 0.5 mg - 1 mg/mL
technique(s) flow cytometry: suitable
western blot: suitable
NCBI登记号 NP_000337
UniProt登记号 P48436
运输 wet ice
储存温度 ?20℃
Gene Information human ... SOX9(6662)

安全信息

储存分类代码 12 - Non Combustible Liquids
WGK WGK 2
闪点(F) Not applicable
闪点(C) Not applicable

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