BCAT1 purified MaxPab mouse polyclonal antibody (B01P)
产品名称： BCAT1 purified MaxPab mouse polyclonal antibody (B01P)
英文名称： BCAT1 purified MaxPab mouse polyclonal antibody (B01P)
产品编号： H00000586-B01P
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:
- Mouse polyclonal antibody raised against a full-length human BCAT1 protein.
- Immunogen:
- BCAT1 (AAH33864, 1 a.a. ~ 320 a.a) full-length human protein.
- Sequence:
- MDCSNGCSAECTGEGGSKEVVGTFKAKDLIVTPATILKEKPDPNNLVFGTVFTDHMLTVEWSSEFGWEKPHIKPLQNLSLHPGSSALHYAVELFEGLKAFRGVDNKIRLFQPNLNMDRMYRSAVRATLPVFDKEELLECIQQLVKLDQEWVPYSTSASLYIRPTFIGTEPSLGVKKPTKALLFVLLSPVGPYFSSGTFNPVSLWANPKYVRAWKGGTGDCKMGGNYGSSLFAQCEAVDNGCQQVLWLYGEDHQITEVGTMNLFLYWINEDGEEELATPPLDGIILPGVTRRCILDLAHQWDTELSLFSINLPDFLQFIYF
- 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 BCAT1 expression in transfected 293T cell line (H00000586-T01) by BCAT1 MaxPab polyclonal antibody.
Lane 1: BCAT1 transfected lysate(35.31 KDa).
Lane 2: Non-transfected lysate. - Protocol Download
- Entrez GeneID:
- 586
- GeneBank Accession#:
- BC033864
- Protein Accession#:
- AAH33864
- Gene Name:
- BCAT1
- Gene Alias:
- BCT1,DKFZp686E12175,ECA39,MECA39,PNAS-121,PP18
- Gene Description:
- branched chain aminotransferase 1, cytosolic
- Omim ID:
- 113520
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes the cytosolic form of the enzyme branched-chain amino acid transaminase. This enzyme catalyzes the reversible transamination of branched-chain alpha-keto acids to branched-chain L-amino acids essential for cell growth. Two different clinical disorders have been attributed to a defect of branched-chain amino acid transamination: hypervalinemia and hyperleucine-isoleucinemia. As there is also a gene encoding a mitochondrial form of this enzyme, mutations in either gene may contribute to these disorders. [provided by RefSeq
- Other Designations:
- branched-chain-amino-acid aminotransferase, cytosolic,placental protein 18