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