SNIP1 anticorps (AA 16-372) (Cy3)

N° du produit ABIN8038060

Cet anticorps anti-SNIP1 Polyclonal Lapin conjugué à Cy3 (ABIN8038060) détecte spécifiquement SNIP1 dans FACS. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour SNIP1 anticorps (AA 16-372) (Cy3) (ABIN8038060)

Antigène: SNIP1 (Smad Nuclear Interacting Protein 1 (SNIP1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SNIP1 est conjugé à/à la Cy3

Application: Flow Cytometry (FACS)

Détail du produit anti-SNIP1 anticorps (Cy3)

Épitope: AA 16-372

Fonction: Anti-SNIP1 Antibody Cy3 Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human SNIP1 recombinant protein (Position: H16-E372).

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, 1-3 μg/1x10⁶ cells

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur SNIP1

Antigène: SNIP1 (Smad Nuclear Interacting Protein 1 (SNIP1))

Autre désignation: SNIP1

Sujet:

Background: Smad nuclear-interacting protein 1 is a protein that in humans is encoded by the SNIP1 gene. This gene encodes a protein that contains a coiled-coil motif and C-terminal forkhead-associated (FHA) domain. The encoded protein functions as a transcriptional coactivator that increases c-Myc activity and inhibits transforming growth factor beta (TGF-beta) and nuclear factor kappa-B (NF-kB) signaling. The encoded protein also regulates the stability of cyclin D1 mRNA, and may play a role in cell proliferation and cancer progression. Mutations in this gene are a cause of psychomotor retardation, epilepsy, and craniofacial dysmorphism (PMRED).

Gene Full Name: Smad nuclear interacting protein 1

ID gène: 79753

UniProt: Q8TAD8

Pathways: SARS-CoV-2 Protein Interactome, Phosphorylation & l'infection par le SRAS-CoV-2