Anti-KDM1/LSD1 antibody - ChIP Grade (ab195405)
Key features and details
- Rabbit polyclonal to KDM1/LSD1 - ChIP Grade
- Suitable for: WB, ChIP, ICC/IF, ChIP-sequencing
- Reacts with: Human
- Isotype: IgG
Overview
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Product name
Anti-KDM1/LSD1 antibody - ChIP Grade
See all KDM1/LSD1 primary antibodies -
Description
Rabbit polyclonal to KDM1/LSD1 - ChIP Grade -
Host species
Rabbit -
Tested applications
Suitable for: WB, ChIP, ICC/IF, ChIP-sequencingmore details -
Species reactivity
Reacts with: Human -
Immunogen
Synthetic peptide within Human KDM1/ LSD1 aa 1-100 (internal sequence) conjugated to keyhole limpet haemocyanin. The exact sequence is proprietary.
Database link: O60341 -
Positive control
- Chromatin prepared from K562 cells; HeLa nuclear extract; HeLa cells.
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General notes
Reproducibility is key to advancing scientific discovery and accelerating scientists’ next breakthrough.
Abcam is leading the way with our range of recombinant antibodies, knockout-validated antibodies and knockout cell lines, all of which support improved reproducibility.
We are also planning to innovate the way in which we present recommended applications and species on our product datasheets, so that only applications & species that have been tested in our own labs, our suppliers or by selected trusted collaborators are covered by our Abpromise™ guarantee.
In preparation for this, we have started to update the applications & species that this product is Abpromise guaranteed for.
We are also updating the applications & species that this product has been “predicted to work with,” however this information is not covered by our Abpromise guarantee.
Applications & species from publications and Abreviews that have not been tested in our own labs or in those of our suppliers are not covered by the Abpromise guarantee.
Please check that this product meets your needs before purchasing. If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, as well as customer reviews and Q&As.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle. -
Storage buffer
Preservatives: 0.05% Sodium azide, 0.05% Proclin 300
Constituent: 99% PBS -
Concentration information loading...
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Purity
Protein A purified -
Clonality
Polyclonal -
Isotype
IgG -
Research areas
Images
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Anti-KDM1/LSD1 antibody - ChIP Grade (ab195405) at 1/4000 dilution + HeLa nuclear extract at 40 µg
Predicted band size: 92 kDaThe antibody was diluted in TBS-Tween containing 5% skimmed milk.
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ChIP results obtained with ab195405 directed against KDM1 / LSD1.
ChIP was performed with ab195405 on sheared chromatin from 4,000,000 K562 cells. An antibody titration consisting of 1, 2, 5 and 10 µg per ChIP experiment was analysed. IgG (2 µg/IP) was used as negative IP control. QPCR was performed with primers for specific regions in the MYT1, RBM19, and TGFBR3 genes, used as positive controls, and for the MYOD1 gene, used as negative control. The figure shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).
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ChIPseq results obtained with ab195405 directed against KDM1 / LSD1.
ChIP was performed on sheared chromatin from 4,000,000 K562 cells using 1 µg of ab195405. The IP’d DNA was subsequently analysed on an Illumina HiSeq. Library preparation, cluster generation and sequencing were performed according to the manufacturer’s instructions. The 50 bp tags were aligned to the human genome using the BWA algorithm. The figure shows the peak distribution along the complete sequence and a 600 kb region of the X-chromosome (figure A and B) and in three regions surrounding the MYT1, RBM19 and TGFBR3 positive control genes, respectively (figure C, D and E). The position of the amplicon used for ChIP-qPCR is indicated by an arrow.
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Immunofluorescenct analysis of HeLa cells labeling KDM1 / LSD1 with ab195405 at 1/200 dilution.
Cells were fixed with 4% formaldehyde for 10 minutes and blocked with PBS/TX-100 containing 5% normal goat serum and 1% BSA. The cells were immunofluorescently labelled with ab195405 (left) diluted in blocking solution followed by an anti-rabbit antibody conjugated to Alexa488. The middle panel shows staining of the nuclei with DAPI. A merge of the two stainings is shown on the right.