SOX2 purified MaxPab rabbit polyclonal antibody (D01P)
产品名称： SOX2 purified MaxPab rabbit polyclonal antibody (D01P)
英文名称： SOX2 purified MaxPab rabbit polyclonal antibody (D01P)
产品编号： H00006657-D01P
产品价格： null
产品产地： 台湾
品牌商标： Abnova
更新时间： null
使用范围：
亚诺法生技股份有限公司（Abnova)
- 联系人 :
- 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
- 邮编 : 11493
- 所在区域 : 台湾
- 电话 : +886-920**1152 点击查看
- 传真 : 点击查看
- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Rabbit polyclonal antibody raised against a full-length human SOX2 protein.
- Immunogen:
- SOX2 (NP_003097.1, 1 a.a. ~ 317 a.a) full-length human protein.
- Sequence:
- MYNMMETELKPPGPQQTSGGGGGNSTAAAAGGNQKNSPDRVKRPMNAFMVWSRGQRRKMAQENPKMHNSEISKRLGAEWKLLSETEKRPFIDEAKRLRALHMKEHPDYKYRPRRKTKTLMKKDKYTLPGGLLAPGGNSMASGVGVGAGLGAGVNQRMDSYAHMNGWSNGSYSMMQDQLGYPQHPGLNAHGAAQMQPMHRYDVSALQYNSMTSSQTYMNGSPTYSMSYSQQGTPGMALGSMGSVVKSEASSSPPVVTSSSHSRAPCQAGDLRDMISMYLPGAEVPEPAAPSRLHMSQHYQSGPVPGTAINGTLPLSHM
- Host:
- Rabbit
- Reactivity:
- Human, Mouse
- Storage Buffer:
- In 1x PBS, pH 7.2
- Storage Instruction:
- Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody reactive against mammalian tissue lysate.
- MSDS:
Download
- Applications
- Western Blot (Tissue lysate)
- SOX2 MaxPab rabbit polyclonal antibody. Western Blot analysis of SOX2 expression in mouse brain.
- Protocol Download
- Entrez GeneID:
- 6657
- GeneBank Accession#:
- NM_003106.2
- Protein Accession#:
- NP_003097.1
- Gene Name:
- SOX2
- Gene Alias:
- ANOP3,MCOPS3,MGC2413
- Gene Description:
- SRY (sex determining region Y)-box 2
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This intronless gene encodes a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of this gene is required for stem-cell maintenance in the central nervous system, and also regulates gene expression in the stomach. Mutations in this gene have been associated with optic nerve hypoplasia and with syndromic microphthalmia, a severe form of structural eye malformation. This gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). [provided by RefSeq
- Other Designations:
- SRY-related HMG-box gene 2,sex-determining region Y-box 2,transcription factor SOX2