YEATS4 antibody (Cat. #AM1885b) western blot analysis in 293 cell line lysates (35ug/lane).This demonstrates the YEATS4 antibody detected the YEATS4 protein (arrow).
YEATS4; GAS41; YEATS domain-containing protein 4; Glioma-amplified sequence 41; NuMA-binding protein 1
Key Feature
Clonality
Monoclonal
Isotype
IgG1
Clone Number
204CT4.7.2
Host Species
Mouse
Tested Applications
WB
WB:1:100~250
Species Reactivity
Human
Concentration
1mg/ml
Target Information
Gene Synonyms
GAS41
Alternative Names
YEATS4 GAS41 YEATS domain-containing protein 4 Glioma-amplified sequence 41 NuMA-binding protein 1
Molecular Weight(MW)
26499 Da
Function
Component of the NuA4 histone acetyltransferase (HAT) complex which is involved in transcriptional activation of select genes principally by acetylation of nucleosomal histones H4 and H2A. This modification may both alter nucleosome - DNA interactions and promote interaction of the modified histones with other proteins which positively regulate transcription. This complex may be required for the activation of transcriptional programs associated with oncogene and proto-oncogene mediated growth induction, tumor suppressor mediated growth arrest and replicative senescence, apoptosis, and DNA repair. NuA4 may also play a direct role in DNA repair when recruited to sites of DNA damage
Tissue Specificity
Expressed in brain, heart, kidney, liver, lung, pancreas, placenta and skeletal muscle
YEATS4 antibody (Cat. #AM1885b) western blot analysis in 293 cell line lysates (35ug/lane).This demonstrates the YEATS4 antibody detected the YEATS4 protein (arrow).
Application Notes
WB:1:100~250
Additional Information
Form
Liquid
Storage Instructions
For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
Storage Buffer
Purified monoclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS.