ARG45670

anti-CHCHD10 antibody

anti-CHCHD10 antibody for Flow cytometry,ICC/IF,IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Monkey,Mouse,Rat

Overview

Product Description Rabbit Polyclonal antibody recognizes CHCHD10
Tested Reactivity Hu, Ms, Rat, Mk
Tested Application FACS, ICC/IF, IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name CHCHD10
Antigen Species Human
Immunogen Recombinant protein containing to human CHCHD10.
Conjugation Un-conjugated
Alternate Names CHCHD10; Coiled-Coil-Helix-Coiled-Coil-Helix Domain Containing 10; C22orf16; N27C7-4; MIX17A; Coiled-Coil-Helix-Coiled-Coil-Helix Domain-Containing Protein 10, Mitochondrial; MIX17 Homolog A; Chromosome 22 Open Reading Frame 16; Protein N27C7-4; FTDALS2; IMMD; SMAJ

Application Instructions

Application Suggestion
Tested Application Dilution
FACS1 - 3 µg/10^6 cells
ICC/IF5 μg/ml
IHC-P2-5 μg/ml
WB0.1-0.25 μg/ml
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Observed Size 15 kDa

Properties

Form Liquid
Purification Affinity purified
Buffer 0.2% Na2HPO4, 0.9% NaCl and 4% Trehalose.
Stabilizer 4% Trehalose
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 400916 Human CHCHD10

Swiss-port # Q8WYQ3 Human Coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochon

Gene Symbol CHCHD10
Gene Full Name Coiled-Coil-Helix-Coiled-Coil-Helix Domain Containing 10
Background 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. [provided by RefSeq, Aug 2014]
Function May be involved in the maintenance of mitochondrial organization and mitochondrial cristae structure. [UniProt]
Cellular Localization Mitochondrion. [UniProt]
Calculated MW 14 kDa
PTM Disulfide bond. [UniProt]