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Read our guarantee »Products:Epigenetics and Nuclear Signaling >> Nuclear Signaling Pathways >> Nuclear Receptors >> Co-activators/co-repressors
Anti-KDM5B / PLU1 / Jarid1B antibody - ChIP Grade
See all KDM5B / PLU1 / Jarid1B products (7) ...
Rabbit polyclonal to KDM5B / PLU1 / Jarid1B - ChIP Grade
WB, IP, ChIP, IHC-Fr, IHC-P, ICC/IFmore details
Reacts with
Mouse, Human
Recombinant fragment, corresponding to amino acids 125-355 of Human PLU1 / Jarid1B
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Whole antiserum
Polyclonal
IgG
Epigenetics and Nuclear Signaling >> ChIP'ing antibodies >> ChIP'ing antibodies
Epigenetics and Nuclear Signaling >> Chromatin Modifying Enzymes >> Jumonji containing proteins
Epigenetics and Nuclear Signaling >> Transcription >> Co-factors
Epigenetics and Nuclear Signaling >> Transcription >> Other factors
Epigenetics and Nuclear Signaling >> Nuclear Signaling Pathways >> Nuclear Receptors >> Co-activators/co-repressors
Our Abpromise guarantee covers the use of ab50958 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: Use at an assay dependent dilution. Predicted molecular weight: 190 kDa.
IP: Use at an assay dependent dilution.
ChIP: Use at an assay dependent dilution.
IHC-Fr: Use at an assay dependent dilution.
IHC-P: 1/300Perform heat mediated antigen retrieval before commencing with IHC staining protocol.
ICC/IF: 1/1000
Histone demethylase that demethylates 'Lys-4' of histone H3, thereby playing a central role in histone code. Does not demethylate histone H3 'Lys-9' or H3 'Lys-27'. Demethylates trimethylated, dimethylated and monomethylated H3 'Lys-4'. Acts as a transcriptional corepressor for FOXG1B and PAX9. Favors the proliferation of breast cancer cells by repressing tumor suppressor genes such as BRCA1 and HOXA5. In contrast, may act as a tumor suppressor for melanoma.
Ubiquitously expressed, with highest levels in testis. Down-regulated in melanoma and glioblastoma. Up-regulated in breast cancer (at protein level).
Belongs to the JARID1 histone demethylase family.
Contains 1 ARID domain.
Contains 1 JmjC domain.
Contains 1 JmjN domain.
Contains 3 PHD-type zinc fingers.
Both the JmjC domain and the JmjN domain are required for enzymatic activity.
The 2 first PHD-type zinc finger domains are required for transcription repression activity.
Nucleus.
Target information above from: UniProt accessionQ9UGL1
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
ChIP - KDM5B / PLU1 / Jarid1B antibody - ChIP Grade (ab50958)

Chromatin was prepared from a whole tissue lysate of mouse skin epidermis according to the Abcam X-ChIP protocol. Cells were fixed with 1% formaldehyde for 10 min. An anti-intergrin V antibody was added to the control, which showed no application. Ab59058 was diluted 1/800 and incubated with the sample for 12 hours at 4°C. The immunoprecipitated DNA was quantified by semiquantitative PCR.
This image is courtesy of an anonymous Abreview
Immunocytochemistry/ Immunofluorescence - KDM5B / PLU1 / Jarid1B antibody - ChIP Grade (ab50958)

ICC/IF image of ab50958 stained HeLa cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab50958, 1/1000 dilution) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM
This product has been referenced in:
See all 7 publications for this product
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Chromatin was prepared from a whole tissue lysate of mouse skin epidermis according to the Abcam X-ChIP protocol. Cells were fixed with 1% formaldehyde for 10 min. An anti-intergrin V antibody was added to the control, which showed no application. Ab59058 was diluted 1/800 and incubated with the sample for 12 hours at 4°C. The immunoprecipitated DNA was quantified by semiquantitative PCR.
This image is courtesy of an anonymous Abreview

ICC/IF image of ab50958 stained HeLa cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab50958, 1/1000 dilution) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM


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