84-4263-55 NDUFA12 100ul 325388
特徴
- 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.
- Applications:Suitable for use in ELISA, Immunohistochemistry.
- Other applications not tested.
- Recommended Dilution:ELISA: 1:1000-1:10,000Immunohistochemistry: 1:50-1:200Optimal dilutions to be determined by the researcher.
- Storage and Stability:May be stored at 4°C for short-term only.
- Aliquot to avoid repeated freezing and thawing.
- Store at -20°C.
- Aliquots are stable for 12 months after receipt.
- For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
仕様
- Size：100ul
- Host：rabbit
- Source Antibody：human
- Grade：Affinity Purified
- Purity：Purified by immunoaffinity chromatography.
- Form：Supplied as a liquid in PBS, pH 7.4, 0.05% sodium azide, 40% glycerol.
- Specificity：Human, Mouse
- Isotype：IgG
- Calc Applications Abbrev：E IHC
- Calc Crossreactivity：Hu Mo
- Immunogen：Synthetic peptide of human NDUFA12
- Shelf Life：1year
- Swiss Prot Number：Q9UI09
- EU Commodity Code：30021010
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