NUBPL Antikörper (AA 1-100) (Cy7)

Produktnummer ABIN6986211

Produktdetails anti-NUBPL Antikörper (Cy7)

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

Bindungsspezifität: AA 1-100

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NUBPL Antikörper ist konjugiert mit Cy7

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

Kreuzreaktivität: Human

Homologie: Mouse,Rat,Dog,Cow,Sheep,Horse

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human NUBPL

Isotyp: IgG

Anwendungsinformationen

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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Konservierungsmittel: ProClin

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

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:

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]

Gen-ID: 80224

UniProt: Q8TB37