CNBD2 anticorps (AA 21-120) (FITC)

N° du produit ABIN1710201

Cet anticorps anti-CNBD2 est un anticorps Lapin Polyclonal détectant CNBD2 dans WB, IF (cc) et IF (p). Adapté pour Humain.

Aperçu rapide pour CNBD2 anticorps (AA 21-120) (FITC) (ABIN1710201)

Antigène: CNBD2 (Cyclic Nucleotide Binding Domain Containing 2 (CNBD2))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CNBD2 est conjugé à/à la FITC

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

Détail du produit anti-CNBD2 anticorps (FITC)

Épitope: AA 21-120

Réactivité croisée: Humain

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

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C20orf152

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 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: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur CNBD2

Antigène: CNBD2 (Cyclic Nucleotide Binding Domain Containing 2 (CNBD2))

Autre désignation: C20orf152

Sujet:

Synonyms: C20orf152, Chromosome 20 open reading frame 152, CT152_HUMAN, dJ954P9.1, RP5-954P9.1, Uncharacterized protein C20orf152, Uncharacterized protein C20orf152 homolog.

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 C20orf152 gene product has been provisionally designated C20orf152 pending further characterization.

ID gène: 140894