C20orf141 anticorps (Biotin)

N° du produit ABIN1404109

Détail du produit anti-C20orf141 anticorps (Biotin)

Antigène: C20orf141 (Chromosome 20 Open Reading Frame 141 (C20orf141))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C20orf141 est conjugé à/à la Biotin

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Réactivité croisée: Humain

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C20ORF141

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400

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: ProClin

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

Stock: -20 °C

Stockage commentaire: Store at -20°C for 12 months.

Date de péremption: 12 months

Détails sur C20orf141

Antigène: C20orf141 (Chromosome 20 Open Reading Frame 141 (C20orf141))

Autre désignation: C20ORF141 (C20orf141 Produits)

Synonymes: anticorps dJ860F19.4, anticorps chromosome 20 open reading frame 141, anticorps chromosome 10 C20orf141 homolog, anticorps C20orf141, anticorps C10H20orf141

Sujet:

Synonyms: LOC128653, Chromosome 20 open reading frame 141, CT141_HUMAN.

Background: The gene encoding C20orf141 maps to human chromosome 20, which houses over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome. Additionally, chromosome 20 contains a region with numerous genes which are thought important for seminal production and may be 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. The C20orf141 gene product has been provisionally designated C20orf141 pending further characterization.

ID gène: 128653