SNIP1 antibody (AA 16-372) (Fluoro647)

Catalog No. ABIN8038068

The Rabbit Polyclonal anti-SNIP1 antibody is suitable to detect SNIP1 in samples from Human. It has been validated for FACS.

Quick Overview for SNIP1 antibody (AA 16-372) (Fluoro647) (ABIN8038068)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SNIP1 antibody is conjugated to Fluoro647

Application: Flow Cytometry (FACS)

Product Details anti-SNIP1 Antibody (Fluoro647)

Binding Specificity: AA 16-372

Purpose: Anti-SNIP1 Antibody Fluoro647 Conjugated

Cross-Reactivity (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

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

Isotype: IgG

Application Details

Application Notes: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Handling

Format: Liquid

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

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

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

Expiry Date: 12 months

Target Details for SNIP1

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

Alternative Name: SNIP1

Background:

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

Gene ID: 79753

UniProt: Q8TAD8

Pathways: SARS-CoV-2 Protein Interactome, The Global Phosphorylation Landscape of SARS-CoV-2 Infection