DATASHEET
Host:
Rabbit
Target Protein:
phospho-KAT5 (Ser86)
Modification Site:
Ser86
Clonality:
Polyclonal
Isotype:
IgG
Entrez Gene:
10524
Swiss Prot:
Q92993
Source:
KLH conjugated synthesised phosphopeptide derived from human KAT5 around the phosphorylation site of Ser86
Purification:
Purified by Protein A.
Storage Buffer:
0.01M TBS(pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Storage:
Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
Background:
Catalytic subunit of the NuA4 histone acetyltransferase 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. Directly acetylates and activates ATM. In case of HIV-1 infection, interaction with the viral Tat protein leads to KAT5 polyubiquitination and targets it to degradation.
PRODUCT SPECIFIC PUBLICATIONS
- Hui Shi. et al. Activation of Galanin Receptor 1 with M617 Attenuates Neuronal Apoptosis via ERK/GSK-3/TIP60 Pathway After Subarachnoid Hemorrhage in Rats. 2021 Jun 04Read more>>
VALIDATION IMAGES
Paraformaldehyde-fixed, paraffin embedded Rat brain; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with KAT5 (Ser86) Polyclonal Antibody, Unconjugated (bs-17096R) at 1:400 overnight at 4°C, DAB staining.
Mouse brain lysates probed with KAT5 (Ser86) Polyclonal Antibody, Unconjugated (bs-17096R) at 1:300 dilution and 4˚C overnight incubation. Followed by conjugated secondary antibody incubation at 1:10000 for 60 min at 37˚C.
Paraformaldehyde-fixed, paraffin embedded (mouse duodenum); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Incubation with (KAT5 (Ser86)) Polyclonal Antibody, Unconjugated (bs-17096R ) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.