FAM209B anticorps (PE)

N° du produit ABIN1712668

Cet anticorps Lapin Polyclonal détecte spécifiquement FAM209B dans WB. Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour FAM209B anticorps (PE) (ABIN1712668)

Antigène: FAM209B (Family with Sequence Similarity 209, Member B (FAM209B))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAM209B est conjugé à/à la PE

Application: Western Blotting (WB)

Détail du produit anti-FAM209B anticorps (PE)

Homologie: Human

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C20orf107

Isotype: IgG

Information d'application

Indications d'application: FCM(1:20-100)

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 FAM209B

Antigène: FAM209B (Family with Sequence Similarity 209, Member B (FAM209B))

Autre désignation: C20orf107

Sujet:

Synonyms: C20orf107, Chromosome 20 open reading frame 107, CT107_HUMAN, dJ1153D9.4, Hypothetical protein LOC388799, MGC104273, Uncharacterized protein C20orf107.

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 C20orf107 gene product has been provisionally designated C20orf107 pending further characterization.

ID gène: 388799