SLMAP antibody (AA 25-607) (FITC)

Catalog No. ABIN8034585

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

Quick Overview for SLMAP antibody (AA 25-607) (FITC) (ABIN8034585)

Target: SLMAP (Sarcolemma Associated Protein (SLMAP))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLMAP antibody is conjugated to FITC

Application: Flow Cytometry (FACS)

Product Details anti-SLMAP Antibody (FITC)

Binding Specificity: AA 25-607

Purpose: Anti-SLMAP Antibody FITC Conjugated

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

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human SLMAP recombinant protein (Position: D25-E607).

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 SLMAP

Target: SLMAP (Sarcolemma Associated Protein (SLMAP))

Alternative Name: SLMAP

Background:

Background: Sarcolemmal membrane-associated protein is a protein that in humans is encoded by the SLMAP gene. This gene encodes a component of a conserved striatin-interacting phosphatase and kinase complex. Striatin family complexes participate in a variety of cellular processes including signaling, cell cycle control, cell migration, Golgi assembly, and apoptosis. The protein encoded by this gene is a coiled-coil, tail-anchored membrane protein with a single C-terminal transmembrane domain that is posttranslationally inserted into membranes. Mutations in this gene are associated with Brugada syndrome, a cardiac channelopathy. Alternative splicing results in multiple transcript variants.

Gene Full Name: sarcolemma associated protein

Gene ID: 7871

UniProt: Q14BN4