NUBPL antibody (AA 1-100) (AbBy Fluor® 488)

Catalog No. ABIN6977691

Product Details anti-NUBPL Antibody (AbBy Fluor® 488)

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

Binding Specificity: AA 1-100

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NUBPL antibody is conjugated to AbBy Fluor® 488

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

Cross-Reactivity: Human

Predicted Reactivity: Mouse,Rat,Dog,Cow,Sheep,Horse

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human NUBPL

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

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.

Preservative: ProClin

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

Storage: -20 °C

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

Expiry Date: 12 months

Target Details for NUBPL

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

Alternative Name: NUBPL (NUBPL Products)

Synonyms: C14orf127 antibody, IND1 antibody, huInd1 antibody, 2410170E07Rik antibody, nucleotide binding protein like antibody, nucleotide binding protein-like antibody, NUBPL antibody, Nubpl antibody

Background:

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]

Gene ID: 80224

UniProt: Q8TB37