Neural Cell Adhesion Molecule 1 (NCAM1) (C-Term) Peptide
NCAM1
Reactivité: Humain
Hôte: Synthetic
BP, WB
N° du produit ABIN980513
150,78 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination:
France
Envoi sous 15 à 22 jours ouvrables
Aperçu rapide pour Neural Cell Adhesion Molecule 1 (NCAM1) (C-Term) Peptide (ABIN980513)
Antigène
CD56 (NCAM1)
(Neural Cell Adhesion Molecule 1 (NCAM1))
Origine
Humain
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB)
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Protein Region
- C-Term
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Séquence
- AFFAKSAAIY NPVIYIMMNK QFRNCMLTTI CCGKNPLGDD EASATVSKTE
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Attributs du produit
- 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.
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Purification
- Purified
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Neural Cell Adhesion Molecule 1 (NCAM1) peptide
NCAM1 Hôte: Synthetic BP, WB, IHC
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Indications d'application
- Each Investigator should determine their own optimal working dilution for specific applications.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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Concentration
- 1 mg/mL
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Buffer
- Final peptide concentration is 1 mg/mL in PBS.
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Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
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Stock
- -20 °C
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Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- CD56 (NCAM1) (Neural Cell Adhesion Molecule 1 (NCAM1))
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Sujet
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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 -
Poids moléculaire
- 39 kDa
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ID gène
- 4684
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NCBI Accession
- NM_181351, NP_851996
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UniProt
- P13591
Antigène
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