FGF13 purified MaxPab mouse polyclonal antibody (B01P)
產品名稱： FGF13 purified MaxPab mouse polyclonal antibody (B01P)
英文名稱： FGF13 purified MaxPab mouse polyclonal antibody (B01P)
產品編號： H00002258-B01P
產品價格： null
產品產地： 臺灣
品牌商標： Abnova
更新時間： null
使用范圍：
亞諾法生技股份有限公司（Abnova)
- 聯系人 :
- 地址 : 臺灣臺北市內湖區洲子街 108 號 9 樓
- 郵編 : 11493
- 所在區域 : 臺灣
- 電話 : +886-920**1152 點擊查看
- 傳真 : 點擊查看
- 郵箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Mouse polyclonal antibody raised against a full-length human FGF13 protein.
- Immunogen:
- FGF13 (NP_004105.1, 1 a.a. ~ 245 a.a) full-length human protein.
- Sequence:
- MAAAIASSLIRQKRQAREREKSNACKCVSSPSKGKTSCDKNKLNVFSRVKLFGSKKRRRRRPEPQLKGIVTKLYSRQGYHLQLQADGTIDGTKDEDSTYTLFNLIPVGLRVVAIQGVQTKLYLAMNSEGYLYTSELFTPECKFKESVFENYYVTYSSMIYRQQQSGRGWYLGLNKEGEIMKGNHVKKNKPAAHFLPKPLKVAMYKEPSLHDLTEFSRSGSGTPTKSRSVSGVLNGGKSMSHNEST
- Host:
- Mouse
- Reactivity:
- Human
- 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 transfected lysate.
- MSDS:
Download
- Applications
- Western Blot (Transfected lysate)
- Western Blot analysis of FGF13 expression in transfected 293T cell line (H00002258-T01) by FGF13 MaxPab polyclonal antibody.
Lane 1: FGF13 transfected lysate(26.95 KDa).
Lane 2: Non-transfected lysate. - Protocol Download
- Entrez GeneID:
- 2258
- GeneBank Accession#:
- NM_004114
- Protein Accession#:
- NP_004105.1
- Gene Name:
- FGF13
- Gene Alias:
- FGF2,FHF2
- Gene Description:
- fibroblast growth factor 13
- Omim ID:
- 300070
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked mental retardation mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini. [provided by RefSeq
- Other Designations:
- OTTHUMP00000024143,OTTHUMP00000024144,fibroblast growth factor homologous factor 2