POU4F3 anticorps (AA 1-180)

N° du produit ABIN6145985

Détail du produit anti-POU4F3 anticorps

Antigène: POU4F3 (POU Domain, Class 4, Transcription Factor 3 (POU4F3))

Épitope: AA 1-180

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp POU4F3 est non-conjugé

Application: Western Blotting (WB)

Séquence: MMAMNSKQPF GMHPVLQEPK FSSLHSGSEA MRRVCLPAPQ LQGNIFGSFD ESLLARAEAL AAVDIVSHGK NHPFKPDATY HTMSSVPCTS TSSTVPISHP AALTSHPHHA VHQGLEGDLL EHISPTLSVS GLGAPEHSVM PAQIHPHHLG AMGHLHQAMG MSHPHTVAPH SAMPACLSDV

Réactivité croisée: Humain

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 1-180 of human POU4F3 (NP_002691.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Commentaires:

HIGH QUALITY

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

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. Avoid freeze / thaw cycles.

Détails sur POU4F3

Antigène: POU4F3 (POU Domain, Class 4, Transcription Factor 3 (POU4F3))

Autre désignation: POU4F3 (POU4F3 Produits)

Synonymes: anticorps POU4F3, anticorps BRN-3, anticorps BRN3, anticorps BRN3C, anticorps DFNA15, anticorps BRN-3.1, anticorps brn-3c, anticorps brn3.1, anticorps brn3c, anticorps Brn3.1, anticorps Brn3c, anticorps ddl, anticorps dreidel, anticorps POU class 4 homeobox 3, anticorps POU domain, class 4, transcription factor 3, anticorps POU4F3, anticorps Pou4f3, anticorps pou4f3

Sujet: This gene encodes a member of the POU-domain family of transcription factors. POU-domain proteins have been observed to play important roles in control of cell identity in several systems. This protein is found in the retina and may play a role in determining or maintaining the identities of a small subset of visual system neurons. Defects in this gene are the cause of non-syndromic sensorineural deafness autosomal dominant type 15.,POU4F3,BRN3C,DFNA15,DFNA42,DFNA52,Epigenetics & Nuclear Signaling,Transcription Factors,Cell Biology & Developmental Biology,Apoptosis,Neuroscience,POU4F3

Poids moléculaire: 37 kDa

ID gène: 5459

UniProt: Q15319

Pathways: Sensory Perception of Sound