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Read our guarantee »Anti-KAT13A / SRC1 antibody [1135/H4] - ChIP Grade
See all KAT13A / SRC1 products (6) ...
Mouse monoclonal [1135/H4] to KAT13A / SRC1 - ChIP Grade
IHC-P, ChIP, Flow Cyt, WB, IPmore details
Reacts with
Mouse, Rat, Human, Monkey
Fusion protein, corresponding to amino acids 477-947 of Human SRC1
Cos cell lysate
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Phosphate buffered saline
Concentration information loading...
Immunogen affinity purified
1 mg/ml of antibody purified from ascites by Protein G chromatography to at least 95% homogeneity as determined by SDS-PAGE. Prepared in 10mM PBS (pH 7.4).
Monoclonal
1135/H4
IgG1
kappa
Metabolism >> Types of disease >> Cancer
Metabolism >> Pathways and Processes >> Metabolic signaling pathways >> Lipid and lipoprotein metabolism >> Lipid metabolism
Cancer >> Cancer Metabolism >> Metabolic signaling pathway >> Metabolism of lipids and lipoproteins
Epigenetics and Nuclear Signaling >> ChIP'ing antibodies >> ChIP'ing antibodies
Cancer >> Oncoproteins/suppressors >> Oncoproteins >> Signal transducers
Epigenetics and Nuclear Signaling >> Chromatin Modifying Enzymes >> Acetylation >> HAT
Epigenetics and Nuclear Signaling >> Nuclear Signaling Pathways >> Nuclear Receptors >> Co-activators/co-repressors
Signal Transduction >> Signaling Pathway >> Nuclear Signaling >> Nuclear Hormone Receptors >> Co-activators/co-repressors
Epigenetics and Nuclear Signaling >> Transcription >> Domain Families >> HLH / Leucine Zipper >> HLH
Epigenetics and Nuclear Signaling >> Chromatin Modifying Enzymes >> Acetylation
Our Abpromise guarantee covers the use of ab84 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-P: Use a concentration of 2 µg/ml.
ChIP: Use 5µl for 106 cells.
Flow Cyt: Use 1µg for 106 cells.
WB: Use a concentration of 0.5 - 2 µg/ml. Predicted molecular weight: 169 kDa.
IP: Use a concentration of 0.5 - 2 µg/ml.
Nuclear receptor coactivator that directly binds nuclear receptors and stimulates the transcriptional activities in a hormone-dependent fashion. Involved in the coactivation of different nuclear receptors, such as for steroids (PGR, GR and ER), retinoids (RXRs), thyroid hormone (TRs) and prostanoids (PPARs). Also involved in coactivation mediated by STAT3, STAT5A, STAT5B and STAT6 transcription factors. Displays histone acetyltransferase activity toward H3 and H4; the relevance of such activity remains however unclear. Plays a central role in creating multisubunit coactivator complexes that act via remodeling of chromatin, and possibly acts by participating in both chromatin remodeling and recruitment of general transcription factors. Required with NCOA2 to control energy balance between white and brown adipose tissues. Required for mediating steroid hormone response. Isoform 2 has a higher thyroid hormone-dependent transactivation activity than isoform 1 and isoform 3.
Widely expressed.
Note=A chromosomal aberration involving NCOA1 is a cause of rhabdomyosarcoma. Translocation t(2;2)(q35;p23) with PAX3 generates the NCOA1-PAX3 oncogene consisting of the N-terminus part of PAX3 and the C-terminus part of NCOA1. The fusion protein acts as a transcriptional activator. Rhabdomyosarcoma is the most common soft tissue carcinoma in childhood, representing 5-8% of all malignancies in children.
Belongs to the SRC/p160 nuclear receptor coactivator family.
Contains 1 basic helix-loop-helix (bHLH) domain.
Contains 1 PAS (PER-ARNT-SIM) domain.
The C-terminal (1107-1441) part mediates the histone acetyltransferase (HAT) activity.
Contains 7 Leu-Xaa-Xaa-Leu-Leu (LXXLL) motifs. LXXLL motifs 3, 4 and 5 are essential for the association with nuclear receptors. LXXLL motif 7, which is not present in isoform 2, increases the affinity for steroid receptors in vitro.
Sumoylated; sumoylation increases its interaction with PGR and prolongs its retention in the nucleus. It does not prevent its ubiquitination and does not exert a clear effect on the stability of the protein.
Ubiquitinated; leading to proteasome-mediated degradation. Ubiquitination and sumoylation take place at different sites.
Phosphorylated upon DNA damage, probably by ATM or ATR.
Nucleus.
Target information above from: UniProt accessionQ15788
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
ChIP - Anti-KAT13A / SRC1 antibody [1135/H4] - ChIP Grade (ab84)
![ChIP - Anti-KAT13A / SRC1 antibody [1135/H4] - ChIP Grade (ab84)](/ps/datasheet/Images/0/ab84/ab84_2.jpg)
Sylvain Daujat
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-KAT13A / SRC1 antibody [1135/H4] - ChIP Grade (ab84)
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-KAT13A / SRC1 antibody [1135/H4] - ChIP Grade (ab84)](/ps/datasheet/images/0/ab84/KAT13A-SRC1-Primary-antibodies-ab84-1.jpg)
ab84 (2µg/ml) staining SRC1 in human colonic mucosa using an automated system (DAKO Autostainer Plus). Using this protocol there is strong nuclear staining of mucosal epithelium and lymphocytes.
Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer EDTA pH 9.0 in a DAKO PT link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako envision flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.
Flow Cytometry-Anti-KAT13A / SRC1 antibody [1135/H4] - ChIP Grade(ab84)
![Flow Cytometry-Anti-KAT13A / SRC1 antibody [1135/H4] - ChIP Grade(ab84)](/ps/datasheet/images/0/ab84/KAT13A-SRC1-Primary-antibodies-ab84-2.jpg)
Overlay histogram showing HeLa cells stained with ab84 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab84, 1µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 2µg/1x106 cells ) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in HeLa cells fixed with 4% paraformaldehyde (10 min)/permeabilized in 0.1% PBS-Tween used under the same conditions.
This product has been referenced in:
See all 4 publications for this product
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![ChIP - Anti-KAT13A / SRC1 antibody [1135/H4] - ChIP Grade (ab84)](/ps/datasheet/Images/0/ab84/ab84_2.jpg)
Sylvain Daujat
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-KAT13A / SRC1 antibody [1135/H4] - ChIP Grade (ab84)](/ps/datasheet/images/0/ab84/KAT13A-SRC1-Primary-antibodies-ab84-1.jpg)
ab84 (2µg/ml) staining SRC1 in human colonic mucosa using an automated system (DAKO Autostainer Plus). Using this protocol there is strong nuclear staining of mucosal epithelium and lymphocytes.
Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer EDTA pH 9.0 in a DAKO PT link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako envision flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.
![Flow Cytometry-Anti-KAT13A / SRC1 antibody [1135/H4] - ChIP Grade(ab84)](/ps/datasheet/images/0/ab84/KAT13A-SRC1-Primary-antibodies-ab84-2.jpg)
Overlay histogram showing HeLa cells stained with ab84 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab84, 1µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (
2
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