RCAN1 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)
-
- 抗原 See all RCAN1 蛋白
- RCAN1 (Regulator of Calcineurin 1 (RCAN1))
- 蛋白类型
- Recombinant
- 产品特性
- Transcript Variant 1
-
宿主
- 人
-
资源
- HEK-293 Cells
- 标记
- This RCAN1 protein is labelled with Myc-DYKDDDDK Tag.
- 应用范围
- Antibody Production (AbP), Standard (STD)
- 产品特性
-
- Recombinant human Calcipressin-1 (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 RCAN1 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
- RCAN1 (Regulator of Calcineurin 1 (RCAN1))
- 别名
- Calcipressin-1 (RCAN1 产品)
- 别名
- ADAPT78 Protein, CSP1 Protein, DSC1 Protein, DSCR1 Protein, MCIP1 Protein, RCN1 Protein, RCAN1 Protein, 2410048A02Rik Protein, AA408855 Protein, AI429645 Protein, AL024459 Protein, AV028423 Protein, Adapt78 Protein, CALP1L Protein, Dscr1 Protein, Mcip1 Protein, dscr1 Protein, rcan1 Protein, wu:fr92c05 Protein, adapt78 Protein, csp1 Protein, dsc1 Protein, mcip1 Protein, MGC53636 Protein, rcn1 Protein, MGC69428 Protein, regulator of calcineurin 1 Protein, regulator of calcineurin 1b Protein, regulator of calcineurin 1 L homeolog Protein, Down syndrome critical region gene 1 Protein, RCAN1 Protein, Rcan1 Protein, rcan1b Protein, rcan1.L Protein, dscr1 Protein, rcan1 Protein
- 背景
- The protein encoded by this gene interacts with calcineurin A and inhibits calcineurin-dependent signaling pathways, possibly affecting central nervous system development. This gene is located in the minimal candidate region for the Down syndrome phenotype, and is overexpressed in the brain of Down syndrome fetuses. Chronic overexpression of this gene may lead to neurofibrillary tangles such as those associated with Alzheimer disease. Alternative splicing results in multiple transcript variants.
- 分子量
- 27.9 kDa
- NCBI登录号
- NP_004405
- 途径
- Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
-