C20orf7 antibody (N-Term)

Catalog No. ABIN2790612

Product Details anti-C20orf7 Antibody

Target: C20orf7 (Chromosome 20 Open Reading Frame 7 (C20orf7))

Binding Specificity: N-Term

Reactivity: Human, Mouse, Rat, Cow, Dog, Pig, Guinea Pig, Rabbit

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C20orf7 antibody is un-conjugated

Application: Western Blotting (WB)

Sequence: TLNIFDRDLK RKQKNWAARQ PEPTKFDYLK EEVGSRIADR VYDIPRNFPL

Predicted Reactivity: Cow: 93%, Dog: 86%, Guinea Pig: 85%, Human: 100%, Mouse: 86%, Pig: 93%, Rabbit: 93%, Rat: 93%

Characteristics: This is a rabbit polyclonal antibody against NDUFAF5. It was validated on Western Blot.

Purification: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the N-terminal region of Human NDUFAF5

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator.

Comment:

Antigen size: 345 AA

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handling Advice: Avoid repeated freeze-thaw cycles.

Storage: -20 °C

Storage Comment: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Target Details for C20orf7

Target: C20orf7 (Chromosome 20 Open Reading Frame 7 (C20orf7))

Alternative Name: NDUFAF5 (C20orf7 Products)

Background: The NADH-ubiquinone oxidoreductase complex (complex I) of the mitochondrial respiratory chain catalyzes the transfer of electrons from NADH to ubiquinone, and consists of at least 43 subunits. The complex is located in the inner mitochondrial membrane. This gene encodes a mitochondrial protein that is associated with the matrix face of the mitochondrial inner membrane and is required for complex I assembly. A mutation in this gene results in mitochondrial complex I deficiency. Multiple transcript variants encoding different isoforms have been found for this gene.
Alias Symbols: FLJ22324, MGC90272, bA526K24.2, dJ842G6.1
Protein Interaction Partner: UBC,
Protein Size: 345

Molecular Weight: 38 kDa

Gene ID: 79133

NCBI Accession: NM_024120, NP_077025

UniProt: Q5TEU4