NUBPL anticorps (AA 1-100) (Cy7)

N° du produit ABIN6986211

Cet anticorps anti-NUBPL est un anticorps Lapin Polyclonal détectant NUBPL dans WB, IF (cc) et IF (p). Adapté pour Humain.

Aperçu rapide pour NUBPL anticorps (AA 1-100) (Cy7) (ABIN6986211)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NUBPL est conjugé à/à la Cy7

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

Détail du produit anti-NUBPL anticorps (Cy7)

Épitope: AA 1-100

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

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