FOXB1 anticorps (full length)

N° du produit ABIN7878244

Cet anticorps anti-FOXB1 Monoclonal Souris (Clone PCRP-FOXB1-1B7) (ABIN7878244) détecte spécifiquement FOXB1 dans ELISA, IF et FACS. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour FOXB1 anticorps (full length) (ABIN7878244)

Antigène: FOXB1 (Forkhead Box B1 (FOXB1))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp FOXB1 est non-conjugé

Application: ELISA, Immunofluorescence (IF), Flow Cytometry (FACS)

Clone: PCRP-FOXB1-1B7

Détail du produit anti-FOXB1 anticorps

Épitope: full length

Fonction: FOXB1 Antibody

Purification: Protein A/G affinity

Immunogène: Recombinant full-length human FOXB1 protein was used as the immunogen for the FOXB1 antibody.

Isotype: IgG1

Information d'application

Indications d'application: Optimal dilution of the FOXB1 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.2 mg/mL

Buffer: 0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced), 0.05 % sodium azide

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: Aliquot the FOXB1 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Détails sur FOXB1

Antigène: FOXB1 (Forkhead Box B1 (FOXB1))

Autre désignation: FOXB1

Sujet: The Forkhead-box (FOX) genes comprise a superfamily of at least 43 members that encode proteins which are involved in transcriptional regulation and may be associated with the pathogenesis of various cancers. FOXB1 (forkhead box B1), also known as FKH5 or HFKH-5, and FOXB2 (forkhead box B2) are members of the FOX family and each contain one forkhead DNA-binding domain. Both FOXB1 and FOXB2 localize to the nucleus where they are thought to function as transcription factors that can bind to DNA via their forkhead domains. In mice, defects in the gene encoding FOXB1 are associated with retarded development of the central nervous system (CNS), suggesting that FOXB1 may play a role in CNS organization and function.

UniProt: Q99853