NDUFB9 Rabbit Polyclonal Antibody (CAB17454)
- SKU:
- CAB17454
- Product Type:
- Antibody
- Reactivity:
- Human
- Mouse
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cell Biology
Frequently bought together:
Description
Product Name: | NDUFB9 Rabbit Polyclonal Antibody |
SKU: | CAB17454 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human,Mouse,Rat |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 80-170 of human NDUFB9 (NP_004996.1). |
Sequence: | YIFP DSPG GTSY ERYD CYKV PEWC LDDW HPSE KAMY PDYF AKRE QWKK LRRE SWER EVKQ LQEE TPPG GPLT EALP PARK EGDL PPLW WYI |
Tested Applications: | WB IHC-P ELISA |
Recommended Dilution: | WB,1:500 - 1:1000 IHC-P,1:50 - 1:200 |
Synonyms: | B22; LYRM3; CI-B22; UQOR22; MC1DN24; NDUFB9 |
Positive Sample: | U-87MG,HepG2,HeLa,Mouse brain,Rat kidney,Rat heart,Rat brain |
Conjugate: | Unconjugated |
Cellular Localization: | Matrix side, Mitochondrion inner membrane, Peripheral membrane protein. |
Calculated MW: | 22kDa |
Observed MW: | 22kDa |
The protein encoded by this gene is a subunit of the mitochondrial oxidative phosphorylation complex I (nicotinamide adenine dinucleotide: ubiquinone oxidoreductase). Complex I is localized to the inner mitochondrial membrane and functions to dehydrogenate nicotinamide adenine dinucleotide and to shuttle electrons to coenzyme Q. Complex I deficiency is the most common defect found in oxidative phosphorylation disorders and results in a range of conditions, including lethal neonatal disease, hypertrophic cardiomyopathy, liver disease, and adult-onset neurodegenerative disorders. Pseudogenes of this gene are found on chromosomes five, seven and eight. Alternative splicing results in multiple transcript variants.
Purification Method: | Affinity purification |
Gene ID: | 4715 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.01% thimerosal,50% glycerol,pH7.3. |