SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
AEBP1-NDUFV1-20-RERE | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-REOR | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-REAQ | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-ORRE | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-OROR | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-ORGO | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-ORAQ | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-GORE | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-GOOR | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-GOGO | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-GOAQ | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-GRGR | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-GRAQ | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-AQRE | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-AQGO | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-AQGR | 20 (40 μL) | 200 μL | Request Pricing | |
AEBP1-NDUFV1-20-AQAQ | 20 (40 μL) | 200 μL | Request Pricing |
This gene encodes a member of carboxypeptidase A protein family. The encoded protein may function as a transcriptional repressor and play a role in adipogenesis and smooth muscle cell differentiation. Studies in mice suggest that this gene functions in wound healing and abdominal wall development. Overexpression of this gene is associated with glioblastoma. [provided by RefSeq, May 2013]
Gene Symbol : AEBP1
Gene Name : AE binding protein 1
Chromosome : CHR 7: 441,043,19-441,145,64
Locus : 7p13
The mitochondrial respiratory chain provides energy to cells via oxidative phosphorylation and consists of four membrane-bound electron-transporting protein complexes (I-IV) and an ATP synthase (complex V). This gene encodes a 51 kDa subunit of the NADH:ubiquinone oxidoreductase complex I; a large complex with at least 45 nuclear and mitochondrial encoded subunits that liberates electrons from NADH and channels them to ubiquinone. This subunit carries the NADH-binding site as well as flavin mononucleotide (FMN)- and Fe-S-biding sites. Defects in complex I are a common cause of mitochondrial dysfunction; a syndrome that occurs in approximately 1 in 10,000 live births. Mitochondrial complex I deficiency is linked to myopathies, encephalomyopathies, and neurodegenerative disorders such as Parkinson's disease and Leigh syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Oct 2009]
Gene Symbol : NDUFV1
Gene Name : NADH:ubiquinone oxidoreductase core subunit V1
Chromosome : CHR 11: 676,068,51-676,125,40
Locus : 11q13.2
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