C20orf194 anticorps (Cy3)

N° du produit ABIN1422017

L’anticorps Lapin Polyclonal anti-C20orf194 a été validé pour WB. Il convient pour détecter C20orf194 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour C20orf194 anticorps (Cy3) (ABIN1422017)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C20orf194 est conjugé à/à la Cy3

Application: Western Blotting (WB)

Détail du produit anti-C20orf194 anticorps (Cy3)

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: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

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

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to 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

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