C20orf194 anticorps

N° du produit ABIN1385790

Détail du produit anti-C20orf194 anticorps

Antigène: C20orf194 (Chromosome 20 Open Reading Frame 194 (C20orf194))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C20orf194 est non-conjugé

Application: Western Blotting (WB)

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C20orf194

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur C20orf194

Antigène: C20orf194 (Chromosome 20 Open Reading Frame 194 (C20orf194))

Autre désignation: C20orf194 (C20orf194 Produits)

Synonymes: anticorps C20orf194, anticorps chromosome 4 open reading frame, human C20orf194, anticorps chromosome 20 open reading frame 194, anticorps C4H20ORF194, anticorps C20orf194

Sujet:

Synonyms: chromosome 20 open reading frame 194, DKFZp434N061, hypothetical protein LOC25943, MGC117480, MGC141683, Uncharacterized protein C20orf194, CT194_HUMAN .

Background: Representing about 2 % of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf194 gene product has been provisionally designated C20orf194 pending further characterization.

ID gène: 25943

UniProt: Q5TEA3