C14orf2 Antikörper

Produktnummer ABIN7248335

Produktdetails anti-C14orf2 Antikörper

Target: C14orf2 (Chromosome 14 Open Reading Frame 2 (C14orf2))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C14orf2 Antikörper ist unkonjugiert

Applikation: ELISA, Immunohistochemistry (IHC), Western Blotting (WB)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Antigen affinity purification

Immunogen: Synthetic peptide of human C14orf2

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000, IHC 1:40-1:200, ELISA 1:5000-1:10000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1.1 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

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

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu C14orf2

Target: C14orf2 (Chromosome 14 Open Reading Frame 2 (C14orf2))

Andere Bezeichnung: C14orf2 (C14orf2 Produkte)

Synonyme: MP68 antikoerper, PLPM antikoerper, MLQ antikoerper, 9430003J03Rik antikoerper, AU043134 antikoerper, AV124504 antikoerper, Mp68 antikoerper, chromosome 14 open reading frame 2 antikoerper, chromosome 21 open reading frame, human C14orf2 antikoerper, RIKEN cDNA 2010107E04 gene antikoerper, C14orf2 antikoerper, C21H14orf2 antikoerper, 2010107E04Rik antikoerper

Hintergrund: C14orf2, also known as MP68, MP68 is a 58 amino acid mitochondrial protein that belongs to the small mitochondrial proteolipid family. The gene encoding MP68 maps to human chromosome 14, which houses over 700 genes and comprises nearly 3.5 % of the human genome. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease (AD). The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder α1-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction.

Molekulargewicht:

Observed_MW: Refer to figures

Calculated_MW: 7 kDa

UniProt: P56378