GTX66245
Mimitin antibody
Cannot supply to this region.
- SKU:
- GTX66245
- Additional Names:
- NADH:ubiquinone oxidoreductase complex assembly factor 2 , B17.2L , MC1DN10 , MMTN , NDUFA12L , mimitin
- Application:
- WB, IF, ICC
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human, Mouse, Rat
- Buffer:
- PBS, 50% Glycerol, 0.02% Sodium azide.
- Immunogen:
- Recombinant funsion protein containing a sequence corresponding to amino acids 1-169 of human NDUFAF2 (NP_777549.1).
- Uniprot:
- Q8N183
- Synonyms:
- B17.2-like;B17.2L;MC1DN10;mimitin;mimitin, mitochondrial;MMTN;Myc-induced mitochondrial protein;NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, assembly factor 2;NADH dehydrogenase (ubiquinone) complex I, assembly factor 2;NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2;NADH dehydrogenase 1 alpha subcomplex assembly factor 2;NDUFA12-like protein;NDUFA12L
- Extra Details:
- NADH:ubiquinone oxidoreductase (complex I) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. This gene encodes a complex I assembly factor. Mutations in this gene cause progressive encephalopathy resulting from mitochondrial complex I deficiency. [provided by RefSeq, Jul 2008]
- Shipping Conditions:
- Blue Ice