NDUFA12 Rabbit Polyclonal Antibody (CAB8237)
- SKU:
- CAB8237
- Product Type:
- Antibody
- Applications:
- WB
- Reactivity:
- Human
- Mouse
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Cell Biology
Frequently bought together:
Description
Product Name: | NDUFA12 Rabbit Polyclonal Antibody |
SKU: | CAB8237 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human,Mouse,Rat |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-145 of human NDUFA12 (NP_061326.1). |
Sequence: | MELV QVLK RGLQ QITG HGGL RGYL RVFF RTND AKVG TLVG EDKY GNKY YEDN KQFF GRHR WVVY TTEM NGKN TFWD VDGS MVPP EWHR WLHS MTDD PPTT KPLT ARKF IWTN HKFN VTGT PEQY VPYS TTRK KIQE WIPP STPY K |
Tested Applications: | WB ELISA |
Recommended Dilution: | WB,1:500 - 1:2000 |
Synonyms: | B17.2; DAP13; MC1DN23; NDUFA12 |
Positive Sample: | 293T,PC-12,HepG2,Mouse kidney,Mouse heart,Mouse testis,Rat heart,Rat brain |
Conjugate: | Unconjugated |
Cellular Localization: | Matrix side, Mitochondrion inner membrane, Peripheral membrane protein. |
Calculated MW: | 17kDa |
Observed MW: | 17kDa |
This gene encodes a protein which is part of mitochondrial complex 1, part of the oxidative phosphorylation system in mitochondria. Complex 1 transfers electrons to ubiquinone from NADH which establishes a proton gradient for the generation of ATP. Mutations in this gene are associated with Leigh syndrome due to mitochondrial complex 1 deficiency. Pseudogenes of this gene are located on chromosomes 5 and 13. Alternative splicing results in multiple transcript variants.
Purification Method: | Affinity purification |
Gene ID: | 55967 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.02% sodium azide,50% glycerol,pH7.3. |