RBBP8NL anticorps (AA 21-120) (Biotin)

N° du produit ABIN1700793

Détail du produit anti-RBBP8NL anticorps (Biotin)

Antigène: RBBP8NL (RBBP8 N-Terminal Like (RBBP8NL))

Épitope: AA 21-120

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp RBBP8NL est conjugé à/à la Biotin

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

Homologie: Human,Mouse,Rat,Cow,Sheep,Pig,Horse,Chicken

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C20orf151

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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 RBBP8NL

Antigène: RBBP8NL (RBBP8 N-Terminal Like (RBBP8NL))

Autre désignation: C20orf151 (RBBP8NL Produits)

Synonymes: anticorps C20H20orf151, anticorps C20orf151, anticorps chromosome 20 C20orf151 homolog, anticorps RBBP8 N-terminal like, anticorps C20H20orf151, anticorps RBBP8NL

Sujet:

Synonyms: C20orf151, Chromosome 20 open reading frame 151, CT151_HUMAN, RP5-908M14.6, Uncharacterized protein C20orf151.

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 C20orf151 gene product has been provisionally designated C20orf151 pending further characterization.

ID gène: 140893