NUBPL Antikörper (AA 1-250)

Produktnummer ABIN2727691

Dieses Anti-NUBPL-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von NUBPL in WB, FACS, IHC und IF. Geeignet für Human.

Kurzübersicht für NUBPL Antikörper (AA 1-250) (ABIN2727691)

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

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser NUBPL Antikörper ist unkonjugiert

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

Klon: 5D5

Produktdetails anti-NUBPL Antikörper

Bindungsspezifität: AA 1-250

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 HEK293T cell.

Isotyp: IgG2b

Anwendungsinformationen

Applikationshinweise: WB 1:2000, IHC 1:150, IF 1:100, 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

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