SDHA Rabbit Monoclonal Antibody (CAB13852)
- SKU:
- CAB13852
- Product Type:
- Antibody
- Reactivity:
- Human
- Mouse
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Monoclonal Antibody
- Research Area:
- Cell Biology
Frequently bought together:
Description
Product Name: | SDHA Rabbit Monoclonal Antibody |
SKU: | CAB13852 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human,Mouse,Rat |
Immunogen: | A synthetic peptide corresponding to a sequence within amino acids 550-650 of human SDHA (P31040). |
Sequence: | KTFD RGMV WNTD LVET LELQ NLML CALQ TIYG AEAR KESR GAHA REDY KVRI DEYD YSKP IQGQ QKKP FEEH WRKH TLSY VDVG TGKV TLEY RPVI DKTL N |
Tested Applications: | WB IF/ICC ELISA |
Recommended Dilution: | WB,1:500 - 1:2000 IF/ICC,1:50 - 1:200 |
Synonyms: | FP; PGL5; SDH1; SDH2; SDHF; CMD1GG; MC2DN1; NDAXOA; SDHA |
Positive Sample: | HeLa,HepG2,MCF7,Mouse liver,Mouse brain,Mouse heart,Rat brain,Rat heart |
Conjugate: | Unconjugated |
Cellular Localization: | Matrix side, Mitochondrion inner membrane, Peripheral membrane protein. |
Calculated MW: | 73kDa |
Observed MW: | 70kDa |
This 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.
Purification Method: | Affinity purification |
Gene ID: | 6389 |
Clone Number: | ARC0726 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.02% sodium azide,0.05% BSA,50% glycerol,pH7.3. |