SLMAP antibody (AA 25-607)

Catalog No. ABIN8034590

This Rabbit Polyclonal antibody specifically detects SLMAP in WB, ELISA and FACS. It exhibits reactivity toward Human and Mouse.

Quick Overview for SLMAP antibody (AA 25-607) (ABIN8034590)

Target: SLMAP (Sarcolemma Associated Protein (SLMAP))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLMAP antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Grade: Carrier-free

Product Details anti-SLMAP Antibody

Binding Specificity: AA 25-607

Purpose: Anti-SLMAP Antibody

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

Characteristics: Anti-SLMAP Antibody. Tested in ELISA, Flow Cytometry, WB applications. This antibody reacts with Human, Mouse.

Purification: Immunogen affinity purified.

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

Isotype: IgG

Application Details

Application Notes: Western blot, 0.25-0.5 μg/mL, Human, Mouse Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human ELISA, 0.1-0.5 μg/mL, -

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Storage: 4 °C,-20 °C

Storage Comment: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

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

Molecular Weight: 95 kDa

Gene ID: 7871

UniProt: Q14BN4