RPL30 positive control ChIP primer pair (ab269262)
Key features and details
- RPL30 positive control ChIP primer pair
- Suitable for: ChIP
Overview
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Product name
RPL30 positive control ChIP primer pair
See all RPL30 primary antibodies -
Description
RPL30 positive control ChIP primer pair -
Tested applications
Suitable for: ChIPmore details -
General notes
Positive control ChIP-qPCR 5' and 3' primers for RPL30 gene. Use with SYBR green.
We recommend these primers as a positive control (based on Abcam's testing) for the histone marks below. They may also be useful for other histone marks.
Suitable positive control for:
- Histone H3 di methyl K36
- Histone H3 acetyl K23
- Histone H3 phospho S10
500pmole of each oligo per unit (lyophilised). HPLC purified, desalted and lyophilised as a sodium salt.Quantity provided is sufficient for approx. 200 reactions based on 2.5pmol of primer per reaction with a final concentration of 100nM in 25µl.
Please contact us after purchase if you require the sequence of the oligos.
Properties
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Form
Lyophilized -
Storage instructions
Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle. -
Concentration information loading... -
Clonality
Monoclonal -
Research areas
Images
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ChIP - RPL30 positive control ChIP primer pair (ab269262)
Chromatin was prepared from HeLa (Human epithelial cells from cervix adenocarcinoma) cells according to the Abcam X-ChIP protocol. HeLa (Human epithelial cells from cervix adenocarcinoma) cells were treated with colcemid at 150ng/ml for 20 h. Treated and non-treated cells were fixed with formaldehyde for 10 minutes. The ChIP was performed with 25µg of chromatin, 2µg of ab177218 (blue), and 20µl of Anti rabbit IgG sepharose beads. 2μg of rabbit normal IgG was added to the beads control (yellow). The immunoprecipitated DNA was quantified by real time PCR (Sybr green approach).
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ChIP - RPL30 positive control ChIP primer pair (ab269262)Chromatin was prepared from HeLa (Human epithelial cell line from cervix adenocarcinoma) cells according to theAbcam X-ChIP protocol. Cells were fixed with formaldehyde for 10 minutes. The ChIP was performed with 25µg of chromatin, 2µg of ab176921 (red), and 20µl of Anti rabbit IgG sepharose beads. 2μg of rabbit normal IgG was added to the beads control (grey). The immunoprecipitated DNA was quantified by real time PCR (Sybr green approach).
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ChIP - RPL30 positive control ChIP primer pair (ab269262)Chromatin was prepared from HeLa (Human epithelial cells from cervix adenocarcinoma) cells according to the Abcam X-ChIP protocol. Cells were fixed with formaldehyde for 10 minutes. The ChIP was performed with 25µg of chromatin, 2µg of ab177275 (blue), and 20µl of Anti Rabbit IgG sepharose beads. 2μg of rabbit normal IgG was added to the beads control (yellow). The immunoprecipitated DNA was quantified by real time PCR (Sybr green approach).
