NUBPL anticorps (AA 1-100) (AbBy Fluor® 647)

N° du produit ABIN6980206

Détail du produit anti-NUBPL anticorps (AbBy Fluor® 647)

Antigène: NUBPL (Nucleotide Binding Protein-Like (NUBPL))

Épitope: AA 1-100

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NUBPL est conjugé à/à la AbBy Fluor® 647

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Réactivité croisée: Humain

Homologie: Mouse,Rat,Dog,Cow,Sheep,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human NUBPL

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur NUBPL

Antigène: NUBPL (Nucleotide Binding Protein-Like (NUBPL))

Autre désignation: NUBPL (NUBPL Produits)

Synonymes: anticorps C14orf127, anticorps IND1, anticorps huInd1, anticorps 2410170E07Rik, anticorps nucleotide binding protein like, anticorps nucleotide binding protein-like, anticorps NUBPL, anticorps Nubpl

Sujet:

Synonyms: C14orf127, FLJ12660, huInd1, IND1 homolog, Iron-sulfur protein NUBPL, Nubpl, NUBPL_HUMAN, nucleotide binding protein like, Nucleotide-binding protein-like.

Background: This gene encodes a member of the Mrp/NBP35 ATP-binding proteins family. The encoded protein is required for the assembly of the respiratory chain NADH dehydrogenase (complex I), an oligomeric enzymatic complex located in the inner mitochondrial membrane. Mutations in this gene cause mitochondrial complex I deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]

ID gène: 80224

UniProt: Q8TB37