SKU: WR5387 Categories: ,

U-Blot® CCDC109A Rabbit mAb

Price range: $268.00 through $328.00

SKU: WR5387-50
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Product details

Background:This gene encodes a calcium transporter that localizes to the mitochondrial inner membrane. The encoded protein interacts with mitochondrial calcium uptake 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012],

Specifications

Size50μL/100μL
TargetCCDC109A
ReactivityHuman, Mouse, Rat
ApplicationsWB, IHC, IF, IP, ELISA
MW(Calculated)40kD
MW(Observed)33kD
Host SpeciesRabbit
IsotypeIgG,Kappa
Conjugate/ModificationUnmodified
Recommended Dilution RatioIHC 1:200-1:1000; WB 1:2000-1:10000; IF 1:200-1:1000; ELISA 1:5000-1:20000; IP 1:50-1:200; / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationPBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
PurificationRecombinant Antibody expressed in animal component-free (ACF) media, purified via Protein A affinity chromatography.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
ClonalityMonoclonal
Clone NumberRM1631R
ImmunogenThe specific immunogen used to produce this antibody is proprietary information.
SpecificityEndogenous
Gene NameMCU
Protein NameCalcium uniporter protein mitochondrial
Other NameMCU; / C10orf42; / CCDC109A; / Calcium uniporter protein; / mitochondrial; / Coiled-coil domain-containing protein 109A
SpeciesHuman
Gene ID90550
UniprotQ8NE86,
Species.1Mouse
Gene ID.1215999
Uniprot.1Q3UMR5
Species.2
Gene ID.2
Uniprot.2
Cellular LocalizationMitochondrion inner membrane; Multi-pass membrane protein .
Tissue ExpressionEye,Testis,
Signaling_pathwayCellular Processes >> Cell growth and death >> Cellular senescence;Organismal Systems >> Immune system >> NOD-like receptor signaling pathway;Human Diseases >> Neurodegenerative disease >> Alzheimer disease;Human Diseases >> Neurodegenerative disease >> Parkinson disease;Human Diseases >> Neurodegenerative disease >> Amyotrophic lateral sclerosis;Human Diseases >> Neurodegenerative disease >> Spinocerebellar ataxia;Human Diseases >> Neurodegenerative disease >> Prion disease;Human Diseases >> Neurodegenerative disease >> Pathways of neurodegeneration - multiple diseases;Environmental Information Processing >> Signal transduction >> Calcium signaling pathway
Research Areas>>Calcium signaling pathway; / >>Cellular senescence; / >>NOD-like receptor signaling pathway; / >>Alzheimer disease; / >>Parkinson disease; / >>Amyotrophic lateral sclerosis; / >>Spinocerebellar ataxia; / >>Prion disease; / >>Pathways of neurodegeneration - multiple diseases
Functionsimilarity:Belongs to the CCDC109 family.,
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