C20orf7 anticorps (N-Term)

N° du produit ABIN2790612

Détail du produit anti-C20orf7 anticorps

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

Épitope: N-Term

Reactivité: Humain, Souris, Rat, Boeuf (Vache), Chien, Porc, Cobaye, Lapin

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C20orf7 est non-conjugé

Application: Western Blotting (WB)

Séquence: TLNIFDRDLK RKQKNWAARQ PEPTKFDYLK EEVGSRIADR VYDIPRNFPL

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

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

Purification: Affinity Purified

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

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator.

Commentaires:

Antigen size: 345 AA

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: Lot specific

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

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeated freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: 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.

Détails sur C20orf7

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

Autre désignation: NDUFAF5 (C20orf7 Produits)

Sujet: 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

Poids moléculaire: 38 kDa

ID gène: 79133

NCBI Accession: NM_024120, NP_077025

UniProt: Q5TEU4