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  • KD/KO Validated

CHCHD10 Polyclonal antibody

CHCHD10 Polyclonal Antibody for WB, IHC, IF/ICC, IP, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat and More (1)

Applications

WB, IHC, IF/ICC, IP, ELISA and More (1)

Conjugate

Unconjugated

Cat No : 25671-1-AP

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Synonyms

CoraLite® Plus 488-conjugated CHCHD10 Polyclonal antibody, Protein N27C7-4, Protein N27C7 4, N27C7 4, Coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial



经过测试的应用

Positive WB detected inHEK-293 cells, mouse brain tissue, HAP1, mouse heart tissue, rat heart tissue
Positive IP detected inmouse heart tissue, HAP1 cells
Positive IHC detected inhuman kidney tissue, human heart tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0
Positive IF/ICC detected inHeLa cells, HAP1
Planning an IF experiment? We recommend our CoraLite® Plus 488 conjugated versions of this antibody.

推荐稀释比

ApplicationDilution
Western Blot (WB)WB : 1:2000-1:10000
Immunoprecipitation (IP)IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate
Immunohistochemistry (IHC)IHC : 1:50-1:500
Immunofluorescence (IF)/ICCIF/ICC : 1:200-1:800
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

产品信息

25671-1-AP targets CHCHD10 in WB, IHC, IF/ICC, IP, ELISA applications and shows reactivity with human, mouse, rat samples.

Tested Applications WB, IHC, IF/ICC, IP, ELISA Application Description
Cited ApplicationsWB, IHC, IP, IF
Tested Reactivity human, mouse, rat
Cited Reactivityhuman, mouse, chicken
Immunogen CHCHD10 fusion protein Ag22598 种属同源性预测
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Full Name coiled-coil-helix-coiled-coil-helix domain containing 10
Synonyms CoraLite® Plus 488-conjugated CHCHD10 Polyclonal antibody, Protein N27C7-4, Protein N27C7 4, N27C7 4, Coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial
Calculated Molecular Weight 14 kDa
Observed Molecular Weight 14 kDa
GenBank Accession NumberBC065232
Gene Symbol CHCHD10
Gene ID (NCBI) 400916
RRIDAB_2880187
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
UNIPROT IDQ8WYQ3
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

CHCHD10 is a mitochondrial protein that is enriched at cristae junctions in the intermembrane space and is likely involved in mitochondrial genome stability and maintenance of cristae junctions. Mutations in CHCHD10 have recently been described as a cause of frontotemporal dementia (FTD) comorbid with amyotrophic lateral sclerosis (ALS).

实验方案

Product Specific Protocols
WB protocol for CHCHD10 antibody 25671-1-APDownload protocol
IHC protocol for CHCHD10 antibody 25671-1-APDownload protocol
IF protocol for CHCHD10 antibody 25671-1-APDownload protocol
IP protocol for CHCHD10 antibody 25671-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

发表文章

SpeciesApplicationTitle
mouseWB,IF

Nat Commun

Loss of function CHCHD10 mutations in cytoplasmic TDP-43 accumulation and synaptic integrity.

Authors - Jung-A A Woo
  • KD Validated
humanWB

Nat Commun

TDP-43 and PINK1 mediate CHCHD10S59L mutation-induced defects in Drosophila and in vitro.

Authors - Minwoo Baek
mouseIHC

J Mol Cell Biol

Single-cell transcriptomes reveal molecular specializations of neuronal cell types in the developing cerebellum.

Authors - Jian Peng
mouseWB

Diabetes

CHCHD10 Modulates Thermogenesis of Adipocytes by Regulating Lipolysis

Authors - Meng Ding
  • KO Validated
mouseWB

Mol Ther Nucleic Acids

Modulation of miR-181 influences dopaminergic neuronal degeneration in a mouse model of Parkinson's disease.

Authors - Colleen S Stein
humanWB,IF

Hum Mol Genet

Loss of CHCHD10-CHCHD2 complexes required for respiration underlies the pathogenicity of a CHCHD10 mutation in ALS.

Authors - Isabella R Straub
  • KD Validated