ATP7B Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)
-
- 抗原 See all ATP7B 蛋白
- ATP7B (ATPase, Cu++ Transporting, beta Polypeptide (ATP7B))
- 蛋白类型
- Recombinant
- 产品特性
- Transcript Variant 1
-
宿主
- 人
-
资源
- HEK-293 Cells
- 标记
- This ATP7B protein is labelled with Myc-DYKDDDDK Tag.
- 应用范围
- Antibody Production (AbP), Standard (STD)
- 产品特性
-
- Recombinant human ATP7B (transcript variant 1) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- 纯度
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product ATP7B 蛋白
-
-
- 应用备注
-
Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - 说明
-
The tag is located at the C-terminal.
- 限制
- 仅限研究用
-
- 浓度
- 50 μg/mL
- 缓冲液
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- 储存条件
- -80 °C
- 储存方法
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
-
- 抗原
- ATP7B (ATPase, Cu++ Transporting, beta Polypeptide (ATP7B))
- 别名
- Atp7b (ATP7B 产品)
- 别名
- PWD Protein, WC1 Protein, WD Protein, WND Protein, Atp7a Protein, tx Protein, Hts Protein, PINA Protein, Wd Protein, ATP7B Protein, ATPase copper transporting beta Protein, ATPase, Cu++ transporting, beta polypeptide Protein, ATPase, Cu++ transporting, beta polypeptide (Wilson disease) Protein, copper-transporting ATPase 2 Protein, ATP7B Protein, Atp7b Protein, atp7b Protein, LOC592143 Protein
- 背景
- This gene is a member of the P-type cation transport ATPase family and encodes a protein with several membrane-spanning domains, an ATPase consensus sequence, a hinge domain, a phosphorylation site, and at least 2 putative copper-binding sites. This protein functions as a monomer, exporting copper out of the cells, such as the efflux of hepatic copper into the bile. Alternate transcriptional splice variants, encoding different isoforms with distinct cellular localizations, have been characterized. Mutations in this gene have been associated with Wilson disease (WD).
- 分子量
- 157.1 kDa
- NCBI登录号
- NP_000044
- 途径
- Transition Metal Ion Homeostasis, Ribonucleoside Biosynthetic Process
-