NUBPL antibody (AA 1-250)

Catalog No. ABIN2727688

Product Details anti-NUBPL Antibody

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

Binding Specificity: AA 1-250

Reactivity: Human

Host: Mouse

Clonality: Monoclonal

Conjugate: This NUBPL antibody is un-conjugated

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

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 E.coli.

Clone: 1C5

Isotype: IgG1

Application Details

Application Notes: WB 1:500~2000, IHC 1:150, 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 (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: 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