Neural Cell Adhesion Molecule 1 (NCAM1) (C-Term) Peptid
NCAM1
Reaktivität: Human
Wirt: Synthetic
BP, WB
Produktnummer ABIN980513
150,78 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach:
Deutschland
Lieferung in 15 bis 22 Werktagen
Kurzübersicht für Neural Cell Adhesion Molecule 1 (NCAM1) (C-Term) Peptid (ABIN980513)
Target
CD56 (NCAM1)
(Neural Cell Adhesion Molecule 1 (NCAM1))
Spezies
Human
Quelle
Synthetic
Applikation
Blocking Peptide (BP), Western Blotting (WB)
-
-
Protein Region
- C-Term
-
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
-
-
Neural Cell Adhesion Molecule 1 (NCAM1) peptide
NCAM1 Wirt: Synthetic BP, WB, IHC
-
-
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.
-
-
- CD56 (NCAM1) (Neural Cell Adhesion Molecule 1 (NCAM1))
-
Hintergrund
-
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
Target
-
Sie sind hier:
