epitope corresponding to amino acids 40-198 mapping near the N-terminus of FOXN4 of mouse origin
Modification Notes
The human gene FOXN4 encodes for a 476 amino acid nuclear protein designated FOXN4. FOXN4 cooperates with key retinogenic factors to mediate the multipotent differentiation of retinal progenitors and is believed to regulate neuronal subtype diversification. FOXN4 is expressed in a subset of mitotic progenitors during retinogenesis. As such, FOXN4 controls the formation of amacrine and horizontal cells by activating the expression of the retinogenic factors MATH-3, Neuro D and PROX1. During spinal neurogenesis, the p2 progenitor domain gives rise to two intermingled distinct subtypes of interneurons, termed V2a and V2b. FOXN4 is coexpressed with the bHLH factor ASH1 (Mash1) in a subset of p2 progenitors. Functionality of FOXN4 affects ASH1 expression and regulates interneuronal formation accordingly. Over-expression of FOXN4 alone in spinal neural progenitors promotes the V2a fate at the expense of the V2b fate, whereas ASH1 suppresses both the V2a and V2b fates.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of FOXN4 of mouse and rat origin by WB, IP, IF and ELISA:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope corresponding to amino acids 40-198 mapping near the N-terminus of FOXN4 of mouse origin
Tissue Specificity
epitope corresponding to amino acids 40-198 mapping near the N-terminus of FOXN4 of mouse origin