SDHA rabbit pAb

SDHA rabbit pAb

AO-06-ES3415-100

SDHA rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES3415
Product nameSDHA rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;IHC
Other nameSDHA; SDH2; SDHF; Succinate dehydrogenase [ubiquinone] flavoprotein subunit; mitochondrial; Flavoprotein subunit of complex II; Fp
Size100μL
Unit price ($)248
Human gene ID6389
Human Swiss-ProtP31040
SourceRabbit
IsotypeIgG
TargetSDHA
Fields>>Citrate cycle (TCA cycle);>>Oxidative phosphorylation;>>Metabolic pathways;>>Carbon metabolism;>>Thermogenesis;>>Non-alcoholic fatty liver disease;>>Alzheimer disease;>>Parkinson disease;>>Amyotrophic lateral sclerosis;>>Huntington disease;>>Prion disease;>>Pathways of neurodegeneration - multiple diseases;>>Chemical carcinogenesis - reactive oxygen species;>>Diabetic cardiomyopathy
Gene nameSDHA
Protein nameSuccinate dehydrogenase [ubiquinone] flavoprotein subunit mitochondrial
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID66945
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ8K2B3
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID157074
Rat gene linkView Rat Gene
Rat Swiss-ProtQ920L2
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human SDHA. AA range:551-600
SpecificitySDHA Polyclonal Antibody detects endogenous levels of SDHA protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000;IHC-p 1:50-300
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)70kD
BackgroundThis gene encodes a major catalytic subunit of succinate-ubiquinone oxidoreductase, a complex of the mitochondrial respiratory chain. The complex is composed of four nuclear-encoded subunits and is localized in the mitochondrial inner membrane. Mutations in this gene have been associated with a form of mitochondrial respiratory chain deficiency known as Leigh Syndrome. A pseudogene has been identified on chromosome 3q29. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2014],
Functioncatalytic activity:Succinate + ubiquinone = fumarate + ubiquinol.,cofactor:FAD.,disease:Defects in SDHA are a cause of complex II mitochondrial respiratory chain deficiency [MIM:252011]; also known as succinate CoQ reductase deficiency. Defects of oxidative phosphorylation give rise to heterogeneous clinical symptoms ranging from isolated organ dysfunction to multisystem disorder. A deficiency of complex II represents a rare cause of mitochondrial encephalomyopathy, leukodystrophy, late-onset optic atrophy and ataxia, myopathy with exercise intolerance, and isolated cardiomyopathy.,disease:Defects in SDHA are a cause of Leigh syndrome (LS) [MIM:256000]. LS is a severe disorder characterized by bilaterally symmetrical necrotic lesions in subcortical brain regions.,function:Flavoprotein (FP) subunit of succinate dehydrogenase (SDH) that is involved in complex II of the mitochondrial electr
Subcellular locationMitochondrion inner membrane ; Peripheral membrane protein ; Matrix side .
ExpressionAdipocyte,Brain,Colon,Heart,Liver,Placenta,

Additional Images

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Western Blot analysis of various cells using SDHA Polyclonal Antibody diluted at 1:2000
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Western Blot analysis of HepG2 cells using SDHA Polyclonal Antibody diluted at 1:2000
Image 3
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Western blot analysis of lysate from HeLa cells, using SDHA antibody.
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Immunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).
: AO-06-ES3415-100
: 10 Items
Hurry! only 10 items left in stock.

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