SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
TRMT61A-NDUFA12-20-RERE | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-REOR | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-REAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-ORRE | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-OROR | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-ORGO | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-ORAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-GORE | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-GOOR | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-GOGO | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-GOAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-GRGR | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-GRAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-AQRE | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-AQGO | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-AQGR | 20 (40 μL) | 200 μL | Request Pricing | |
TRMT61A-NDUFA12-20-AQAQ | 20 (40 μL) | 200 μL | Request Pricing |
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. [provided by RefSeq, Apr 2012]
Gene Symbol : NDUFA12
Gene Name : NADH:ubiquinone oxidoreductase subunit A12
Chromosome : CHR 12: 950,037,12-949,713,27
Locus : 12q22
Gene Symbol : TRMT61A
Gene Name : TRNA methyltransferase 61A
Chromosome : CHR 14: 103,529,171-103,537,072
Locus : 14q32.33
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