NDUFA2 Muis Monoklonale Antilichaam [Kloon ID: LBI5A5]

The encoded protein is a subunit of the hydrophobic protein fraction of the NADH:ubiquinone oxidoreductase (complex 1), the first enzyme complex in the electron transport chain located in the inner mitochondrial membrane, and may be involved in regulating complex I activity or its assembly via assistance in redox processes. Mutations in this gene are associated with Leigh syndrome, an early-onset progressive neurodegenerative disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]

Carrier-free (BSA/glycerol-free) NDUFA2 mouse monoclonal antibody, clone LBI5A5

B8; CD14; CIB8

Homo sapiens NADH:ubiquinone oxidoreductase subunit A2 (NDUFA2), transcript variant 1, mRNA.

4695

O43678

Unconjugated

Alzheimer's disease, Huntington's disease, Metabolic pathways, Oxidative phosphorylation, Parkinson's disease

Alzheimer's disease, Huntington's disease, Metabolic pathways, Oxidative phosphorylation, Parkinson's disease

IHC 1:150

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

NDUFA2

https://www.ncbi.nlm.nih.gov/gene/?term=4695

https://www.uniprot.org/uniprot/O43678