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Proprotein Convertase 1/3 (C-Term) anticorps

L’anticorps anti-Proprotein Convertase 1/3 Polyclonal Lapin est utilisé pour la détection de Proprotein Convertase 1/3 dans des échantillons de Humain, Souris et Rat. Il a été validé pour IHC (p) et WB.
N° du produit ABIN3029753
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour Proprotein Convertase 1/3 (C-Term) anticorps (ABIN3029753)

Antigène

Proprotein Convertase 1/3

Reactivité

Humain, Souris, Rat

Hôte

Lapin

Clonalité

Polyclonal

Application

Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Western Blotting (WB)
  • Épitope

    C-Term

    Purification

    Antigen affinity

    Immunogène

    An amino acid sequence from the C-terminus of human Proprotein Convertase 1/3 (DVFYNTKPYKHRDDR) was used as the immunogen for this Proprotein Convertase 1/3 antibody (100% homologous in human, mouse and rat).

    Isotype

    IgG
  • Indications d'application

    The stated application concentrations are suggested starting amounts. Titration of the Proprotein Convertase 1/3 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 0.5-1 μg/mL,IHC (Paraffin): 0.5-1 μg/mL

    Restrictions

    For Research Use only
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    -20 °C

    Stockage commentaire

    After reconstitution, the Proprotein Convertase 1/3 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Antigène

    Proprotein Convertase 1/3

    Sujet

    Proprotein Convertase, Subtilisin/Kexin-Type, 1, also known as PC1 or NEC1, is an enzyme that in humans is encoded by the PCSK1 gene. It is a neuroendocrine convertase that belongs to a family of subtilisin-like serine endoproteases that process large precursor proteins into mature bioactive products. By in situ hybridization, Seidah et al.(1991) mapped the gene to human chromosome 5q15-q21 and mouse chromosome 13. Ohagi et al.(1996) noted that PCSK1 initiates the sequential processing of proinsulin to insulin by cleaving the proinsulin molecule on the C-terminal side of the dibasic peptide, arg31-arg32, joining the B-chain and C-peptide. By observing the phenotypic features in patients with PCSK1 mutations, Jackson et al.(2003) concluded that human intestinal absorptive function is dependent on the enzymes activity.

    UniProt

    P29120
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