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Anti kmt1c g9a

Manufactured by Abcam

Anti-KMT1C/G9a is a primary antibody that specifically binds to the KMT1C/G9a protein, which is a histone methyltransferase enzyme responsible for mono- and di-methylation of histone H3 at lysine 9 (H3K9me1 and H3K9me2).

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2 protocols using anti kmt1c g9a

1

Epigenetic Analysis of GFP-RNase H1 in Mammalian Cells

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Transfections of GFP-RNase H1 plasmid into human HeLa and mouse embryonic fibroblasts (MEF) cells were carried out as described previously4 . Ago2 KO and parental wild type cells are MEFs. G9a/GLP double KO and their parental wild type are mouse embryonic stem (mES) cells. Treatment with 10 μM of BIX-01294 inhibitor (Sigma) was performed as described20 (link). Total RNA was isolated using TRIzol reagent (Invitrogen) and reverse transcribed with SuperScript III Reverse Transcriptase (Invitrogen) using gene-specific primers. J2 dsRNA pull-down was performed as described8 (link). RT-qPCR levels are presented graphically as raw values x1000. Chromatin immuno-precipitation (ChIP) and genomic DNA immuno-precipitation (DIP) analyses were carried out as before4 . The following antibodies were used for ChIP: anti-H3K9me2 (Abcam), anti-H3K9me3 (Abcam), anti-H3 (Abcam), anti-Dicer (13D6) (Abcam), anti-KMT1C/G9a (Abcam), anti-Ago1 (Millipore), anti-Ago2 (Abcam) and anti-Pol II (H-224) (Santa Cruz Biotechnology). S9.6 RNA:DNA hybrid specific antibody was used for DIP4
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2

Epigenetic Analysis of GFP-RNase H1 in Mammalian Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
Transfections of GFP-RNase H1 plasmid into human HeLa and mouse embryonic fibroblasts (MEF) cells were carried out as described previously4 . Ago2 KO and parental wild type cells are MEFs. G9a/GLP double KO and their parental wild type are mouse embryonic stem (mES) cells. Treatment with 10 μM of BIX-01294 inhibitor (Sigma) was performed as described20 (link). Total RNA was isolated using TRIzol reagent (Invitrogen) and reverse transcribed with SuperScript III Reverse Transcriptase (Invitrogen) using gene-specific primers. J2 dsRNA pull-down was performed as described8 (link). RT-qPCR levels are presented graphically as raw values x1000. Chromatin immuno-precipitation (ChIP) and genomic DNA immuno-precipitation (DIP) analyses were carried out as before4 . The following antibodies were used for ChIP: anti-H3K9me2 (Abcam), anti-H3K9me3 (Abcam), anti-H3 (Abcam), anti-Dicer (13D6) (Abcam), anti-KMT1C/G9a (Abcam), anti-Ago1 (Millipore), anti-Ago2 (Abcam) and anti-Pol II (H-224) (Santa Cruz Biotechnology). S9.6 RNA:DNA hybrid specific antibody was used for DIP4
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