Neural Cell Adhesion Molecule 1 (NCAM1) (C-Term) Peptide
NCAM1
适用: 人
宿主: 合成
BP, WB
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- 抗原 See all CD56 (NCAM1) products
- CD56 (NCAM1) (Neural Cell Adhesion Molecule 1 (NCAM1))
- 蛋白结构域
- C-Term
- 宿主
- 人
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资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB)
- 序列
- AFFAKSAAIY NPVIYIMMNK QFRNCMLTTI CCGKNPLGDD EASATVSKTE
- 产品特性
- This is a synthetic peptide designed for use in combination with anti-NCAM1 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- 纯化方法
- Purified
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- 应用备注
- Each Investigator should determine their own optimal working dilution for specific applications.
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- 浓度
- 1 mg/mL
- 缓冲液
- Final peptide concentration is 1 mg/mL in PBS.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- 抗原
- CD56 (NCAM1) (Neural Cell Adhesion Molecule 1 (NCAM1))
- 别名
- CD56 Peptide, MSK39 Peptide, NCAM Peptide, fj56g09 Peptide, ncam Peptide, ncam1 Peptide, wu:fj56g09 Peptide, NCAM1 Peptide, n-cam Peptide, E-NCAM Peptide, NCAM-1 Peptide, Ncam Peptide, Cd56 Peptide, N-CAM Peptide, N-CAM-1 Peptide, NCAM-C Peptide, NCAMC Peptide, N-CAM-1-B Peptide, NCAM-1-B Peptide, ncam1-a Peptide, ncam1-b Peptide, neural cell adhesion molecule 1 Peptide, neural cell adhesion molecule 1a Peptide, neural cell adhesion molecule 1 S homeolog Peptide, neural cell adhesion molecule 1 L homeolog Peptide, NCAM1 Peptide, ncam1a Peptide, ncam1 Peptide, LOC100085373 Peptide, ncam1.S Peptide, Ncam1 Peptide, ncam1.L Peptide
- 背景
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Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which comprises about 25 % of total cases, approximately 30 % of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which, when photoexcited, initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness.
Alias Symbols: CD56, MSK39, NCAM
Protein Interaction Partner: ADRBK1,ARR3,GNGT1,GRK1,GRK5,GRK6,PPP2CA,PRKCA,SAG,ADRBK1,ARR3,GRK1,GRK5,RHO,SAG,UBC
Protein Size: 348 - 分子量
- 39 kDa
- 基因ID
- 4684
- NCBI登录号
- NM_181351, NP_851996
- UniProt
- P13591
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