CHCHD10 antibody (AA 80-142) (Fluoro488)

Catalog No. ABIN7980965

The Fluoro488-conjugated Rabbit Polyclonal anti-CHCHD10 antibody (ABIN7980965) specifically detects CHCHD10 in FACS. The antibody is reactive with Human, Mouse, Monkey and Rat samples.

Quick Overview for CHCHD10 antibody (AA 80-142) (Fluoro488) (ABIN7980965)

Target: CHCHD10 (Coiled-Coil-Helix-Coiled-Coil-Helix Domain Containing 10 (CHCHD10))

Reactivity: Human, Mouse, Monkey, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CHCHD10 antibody is conjugated to Fluoro488

Application: Flow Cytometry (FACS)

Product Details anti-CHCHD10 Antibody (Fluoro488)

Binding Specificity: AA 80-142

Purpose: Anti-CHCHD10 Antibody Fluoro488 Conjugated

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

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human CHCHD10 recombinant protein (Position: P80-P142).

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 CHCHD10

Target: CHCHD10 (Coiled-Coil-Helix-Coiled-Coil-Helix Domain Containing 10 (CHCHD10))

Alternative Name: CHCHD10

Background:

Background: Coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial, also known as Protein N27C7-4 is a protein that in humans is encoded by the CHCHD10 gene. This gene encodes a mitochondrial protein that is enriched at cristae junctions in the intermembrane space. It may play a role in cristae morphology maintenance or oxidative phosphorylation. Mutations in this gene cause frontotemporal dementia and/or amyotrophic lateral sclerosis-2. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 7 and 19.

Gene Full Name: coiled-coil-helix-coiled-coil-helix domain containing 10

Gene ID: 400916

UniProt: Q8WYQ3