NUBPL antibody (AA 1-250)

Catalog No. ABIN2727691

This anti-NUBPL antibody is a Mouse Monoclonal antibody detecting NUBPL in WB, FACS, IHC and IF. Suitable for Human.

Quick Overview for NUBPL antibody (AA 1-250) (ABIN2727691)

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

Reactivity: Human

Host: Mouse

Clonality: Monoclonal

Conjugate: This NUBPL antibody is un-conjugated

Application: Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (IHC), Immunofluorescence (IF)

Clone: 5D5

Product Details anti-NUBPL Antibody

Binding Specificity: AA 1-250

Characteristics: Homo sapiens nucleotide binding protein-like (NUBPL), transcript variant 1

Purification: Purified from mouse ascites fluids by affinity chromatography

Immunogen: Human recombinant protein fragment corresponding to amino acids 1-250 of human NUBPL(NP_079428) produced in HEK293T cell.

Isotype: IgG2b

Application Details

Application Notes: WB 1:2000, IHC 1:150, IF 1:100, FLOW 1:100,

Comment:

The concentration of the product may vary between diferrent lots.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.5-1.0 mg/mL

Buffer: PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.

Preservative: Sodium azide

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

Storage: -20 °C

Target Details for NUBPL

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

Alternative Name: NUBPL

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. The respiratory complex I consists of 45 subunits and 8 iron-sulfur (Fe/S) clusters. This protein is an Fe/S protein that plays a critical role in the assembly of respiratory complex I, likely by transferring Fe/S into the Fe/S-containing complex I subunits. Mutations in this gene cause mitochondrial complex I deficiency. Alternatively spliced transcript variants encoding distinct isoforms have been identified.

Molecular Weight: 33.9 kDa

Gene ID: 80224

NCBI Accession: NM_025152

HGNC: 80224