NDUFAF2 Protein (Myc-DYKDDDDK Tag)

Catalog No. ABIN2726016

Product Details

Target: NDUFAF2 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 2 (NDUFAF2))

Protein Type: Recombinant

Origin: Human

Source: HEK-293 Cells

Purification tag / Conjugate: This NDUFAF2 protein is labelled with Myc-DYKDDDDK Tag.

Application: Antibody Production (AbP), Standard (STD)

Characteristics:

• Recombinant human Mimitin protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Purity: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Application Details

Application Notes: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Comment:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Handling

Concentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Storage: -80 °C

Storage Comment: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Target Details

Target: NDUFAF2 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 2 (NDUFAF2))

Alternative Name: Mimitin (NDUFAF2 Products)

Synonyms: B17.2L Protein, MMTN Protein, NDUFA12L Protein, mimitin Protein, Ndufa12l Protein, RGD1560158 Protein, NDUFAF2 Protein, ndufa12l Protein, zgc:101036 Protein, 1810058I14Rik Protein, C86051 Protein, NADH:ubiquinone oxidoreductase complex assembly factor 2 Protein, NADH:ubiquinone oxidoreductase complex assembly factor 2 L homeolog Protein, NADH dehydrogenase (ubiquinone) complex I, assembly factor 2 Protein, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, assembly factor 2 Protein, NDUFAF2 Protein, Ndufaf2 Protein, ndufaf2.L Protein, ndufaf2 Protein

Background: 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.

Molecular Weight: 19.7 kDa

NCBI Accession: NP_777549

Pathways: SARS-CoV-2 Protein Interactome