Neural Cell Adhesion Molecule 1 (NCAM1) (C-Term) Peptid
NCAM1
Reaktivität: Human
Wirt: Synthetic
BP, WB
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- Target Alle CD56 (NCAM1) Produkte
- CD56 (NCAM1) (Neural Cell Adhesion Molecule 1 (NCAM1))
- Protein Region
- C-Term
- Spezies
- Human
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Quelle
- Synthetic
- Applikation
- Blocking Peptide (BP), Western Blotting (WB)
- Sequenz
- AFFAKSAAIY NPVIYIMMNK QFRNCMLTTI CCGKNPLGDD EASATVSKTE
- Produktmerkmale
- 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.
- Aufreinigung
- Purified
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-
- Applikationshinweise
- Each Investigator should determine their own optimal working dilution for specific applications.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
- Format
- Lyophilized
- Rekonstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Konzentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handhabung
- Avoid repeated freeze-thaw cycles.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- CD56 (NCAM1) (Neural Cell Adhesion Molecule 1 (NCAM1))
- Synonyme
- 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
- Hintergrund
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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 - Molekulargewicht
- 39 kDa
- Gen-ID
- 4684
- NCBI Accession
- NM_181351, NP_851996
- UniProt
- P13591
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