NUBPL Antikörper (AA 1-250)

Produktnummer ABIN2727688

Produktdetails anti-NUBPL Antikörper

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

Bindungsspezifität: AA 1-250

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser NUBPL Antikörper ist unkonjugiert

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

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

Aufreinigung: 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.

Klon: 1C5

Isotyp: IgG1

Anwendungsinformationen

Applikationshinweise: WB 1:500~2000, IHC 1:150, FLOW 1:100,

Kommentare:

The concentration of the product may vary between diferrent lots.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.5-1.0 mg/mL

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

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Details zu NUBPL

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

Andere Bezeichnung: NUBPL (NUBPL Produkte)

Synonyme: C14orf127 antikoerper, IND1 antikoerper, huInd1 antikoerper, 2410170E07Rik antikoerper, nucleotide binding protein like antikoerper, nucleotide binding protein-like antikoerper, NUBPL antikoerper, Nubpl antikoerper

Hintergrund: 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.

Molekulargewicht: 33.9 kDa

Gen-ID: 80224

NCBI Accession: NM_025152

HGNC: 80224