SDHA Mouse mAb - Primary antibody, specific to SDHA, Mouse IgG2a

Features and benefits
  • Short Overview:

    mAb (C2); Mouse anti Human SDHA Antibody; WB, ICC, IF; Unconjugated

  • Species reactivity(Reacts with): Human,Mouse,Rat
  • Isotype: Mouse IgG2a
    Application:
  • IF/ICC
  • WB
Item Number
Ab126844
Grouped product items
SKUSizeAvailabilityPrice Qty
Ab126844-10μl
10μl
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$66.90
Ab126844-20μl
20μl
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$768.90
Ab126844-50μl
50μl
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$199.90
Ab126844-100μl
100μl
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$299.90
Ab126844-1ml
1ml
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$2,299.90

mAb (C2); Mouse anti Human SDHA Antibody; WB, ICC, IF; Unconjugated

Basic Description

Product NameSDHA Mouse mAb - Primary antibody, specific to SDHA, Mouse IgG2a
SynonymsCMD1GG antibody; DHSA_HUMAN antibody; Flavoprotein subunit of complex II antibody; Fp antibody; PGL5 antibody; SDH 2 antibody; SDH1 antibody; SDH2 antibody; SDHA antibody; SDHF antibody; Succinate dehydrogenase [ubiquinone] flavoprotein subunit antibody;
Specifications & PurityExactAb™, Validated, Carrier Free, Azide Free, High performance, Lot by Lot
Host speciesMouse
SpecificitySDHA
ImmunogenRecombinant SDHA expressed in E.coli (AA 4-300)
Positive ControlWB: Hep G2, HeLa, MCF7, A549, LNCaP, HEK293, NIH/3T3 and C6 cell lysates. ICC/IF: HeLa cells.
ConjugationUnconjugated
GradeAzide Free, Carrier Free, ExactAb™, High Performance, Validated
Product Description

Mouse anti Human SDHA Antibody, Monoclonal (C2), could be used for WB, ICC, IF and so on.
Application
WB:0.01-2µg/mL
ICC/IF:5-30µg/mL
Protein Function
Flavoprotein (FP) subunit of succinate dehydrogenase (SDH) that is involved in complex II of the mitochondrial electron transport chain and is responsible for transferring electrons from succinate to ubiquinone (coenzyme Q).

Product Properties

IsotypeMouse IgG2a
Light Chain Typekappa
SDS-PAGE150 kDa
Purification MethodProtein A and Protein G purified
FormLiquid
ConcentrationLot by Lot
Storage TempStore at -20°C,Avoid repeated freezing and thawing
Shipped InIce chest + Ice pads
Stability And StorageStore at 4℃ short term (1-2 weeks). Store at -20℃ long term (24 months). Upon delivery aliquot. Avoid freeze/thaw cycle.

Images

SDHA Mouse mAb (Ab126844) - Western Blot
All lanes: SDHA Mouse mAb (Ab126844) at 1/1000 dilution
Samples: Lysates at 20 µg per lane
Secondary: Goat Anti-Mouse IgG H&L (HRP) (Ab138040) at 1/20000 dilution

Predicted band size: 70 kDa
Observed band size: 66 kDa
Exposure time: 2.5 s

SDHA Mouse mAb (Ab126844) - IF/ICC
FITC staining on IF
Samples: Human HeLa cells
Primary Ab: 30 µg/mL SDHA Mouse mAb (Ab126844)
Second Ab: 2 µg/mL FITC-Linked Caprine Anti-Mouse IgG Polyclonal Antibody.

Associated Targets(Human)

SDHA Tbio Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SDHA Tbio Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial (4 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Application

ApplicationDilution info
WB

0.01-2 µg/mL

ICC/IF

5-30 µg/mL

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

Find and download the COA for your product by matching the lot number on the packaging.

3 results found

Lot NumberCertificate TypeDateItem
ZJ24F0505914Certificate of AnalysisMay 21, 2024 Ab126844
ZJ23F0901139Certificate of AnalysisSep 24, 2023 Ab126844
ZJ23F0901138Certificate of AnalysisSep 24, 2023 Ab126844

Related Documents

References

1. Choudhary C, Kumar C, Gnad F, Nielsen ML, Rehman M, Walther TC, Olsen JV, Mann M.  (2009)  Lysine acetylation targets protein complexes and co-regulates major cellular functions..  Science,  325  (5942): (834-40).  [PMID:19608861]
2. G Herma Renkema,Saskia B Wortmann,Roel J Smeets,Hanka Venselaar,Marion Antoine,Gepke Visser,Tawfeg Ben-Omran,Lambert P van den Heuvel,Henri J L M Timmers,Jan A Smeitink,Richard J T Rodenburg.  (2014-05-02)  SDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumors..  European journal of human genetics : EJHG,  23  ((2)): (202-209).  [PMID:24781757]
3. Bourgeron, T T and 7 more authors..  (1995)  Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency..  Nature genetics,      [PMID:7550341]
4. Hirawake, H H, Wang, H H, Kuramochi, T T, Kojima, S S and Kita, K K..  (1994)  Human complex II (succinate-ubiquinone oxidoreductase): cDNA cloning of the flavoprotein (Fp) subunit of liver mitochondria..  Journal of biochemistry,      [PMID:7798181]
5. Morris, A A AA, Farnsworth, L L, Ackrell, B A BA, Turnbull, D M DM and Birch-Machin, M A MA..  (1994)  The cDNA sequence of the flavoprotein subunit of human heart succinate dehydrogenase..  Biochimica et biophysica acta,    (29):   [PMID:8142412]
6. Parfait, B B and 5 more authors..  (2000)  Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome..  Human genetics,      [PMID:10746566]
7. Birch-Machin, M A MA, Taylor, R W RW, Cochran, B B, Ackrell, B A BA and Turnbull, D M DM..  (2000)  Late-onset optic atrophy, ataxia, and myopathy associated with a mutation of a complex II gene..  Annals of neurology,      [PMID:10976639]
8. Van Coster, Rudy R and 9 more authors..  (2003)  Homozygous Gly555Glu mutation in the nuclear-encoded 70 kDa flavoprotein gene causes instability of the respiratory chain complex II..  American journal of medical genetics. Part A,    (1):   [PMID:12794685]
9. Aboulaich, Nabila N, Vainonen, Julia P JP, Strålfors, Peter P and Vener, Alexander V AV..  (2004)  Vectorial proteomics reveal targeting, phosphorylation and specific fragmentation of polymerase I and transcript release factor (PTRF) at the surface of caveolae in human adipocytes..  The Biochemical journal,    (15):   [PMID:15242332]
10. Schmutz, Jeremy J and 75 more authors..  (2004)  The DNA sequence and comparative analysis of human chromosome 5..  Nature,    (16):   [PMID:15372022]
11. Hao, Huai-Xiang HX and 13 more authors..  (2009)  SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma..  Science (New York, N.Y.),    (28):   [PMID:19628817]
12. Burnichon, Nelly N and 13 more authors..  (2010)  SDHA is a tumor suppressor gene causing paraganglioma..  Human molecular genetics,    (1):   [PMID:20484225]
13. Levitas, Aviva A and 8 more authors..  (2010)  Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase..  European journal of human genetics : EJHG,      [PMID:20551992]
14. Ogura, Masato; Yamaki, Junko; Homma, Miwako K and Homma, Yoshimi..  (2012)  Mitochondrial c-Src regulates cell survival through phosphorylation of respiratory chain components..  The Biochemical journal,    (15):   [PMID:22823520]
15. Alston, Charlotte L CL and 12 more authors..  (2012)  Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency..  Journal of medical genetics,      [PMID:22972948]
16. Sciacovelli, Marco M and 12 more authors..  (2013)  The mitochondrial chaperone TRAP1 promotes neoplastic growth by inhibiting succinate dehydrogenase..  Cell metabolism,    (4):   [PMID:23747254]
17. Helman, Guy G and 13 more authors..  (2016)  Magnetic resonance imaging spectrum of succinate dehydrogenase-related infantile leukoencephalopathy..  Annals of neurology,      [PMID:26642834]
18. Courage, Carolina C and 6 more authors..  (2017)  SDHA mutation with dominant transmission results in complex II deficiency with ocular, cardiac, and neurologic involvement..  American journal of medical genetics. Part A,      [PMID:27683074]
19. Lahiri, Amit A, Hedl, Matija M, Yan, Jie J and Abraham, Clara C..  (2017)  Human LACC1 increases innate receptor-induced responses and a LACC1 disease-risk variant modulates these outcomes..  Nature communications,    (8):   [PMID:28593945]

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