17-10491
ChIPAb+ MeCP2 - ChIP Validated Antibody and Primer Set
from chicken, purified by affinity chromatography
Synonym(s):
Methyl CpG binding protein 2, MeCp-2 protein, MeCp2
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About This Item
biological source
chicken
clone
polyclonal
purified by
affinity chromatography
species reactivity
mouse, rat, human
manufacturer/tradename
ChIPAb+
Upstate®
technique(s)
ChIP: suitable
immunoprecipitation (IP): suitable
western blot: suitable
isotype
IgY
NCBI accession no.
UniProt accession no.
shipped in
dry ice
Gene Information
human  ...  MECP2(4204)   
General description
The ChIPAb+ MECP2 set includes a MECP2 antibody, a Normal Chicken IgY (both with bridging antibody included), and positive control primers which amplify 144 bp of a human SNRPN intron region. The MECP2 antibody and negative control IgG are supplied in a scalable "per ChIP" reaction size and can be used to functionally validate the precipitation of MECP2 associated chromatin.
Immunogen
Application
Chromatin Immunoprecipitation:
Sonicated chromatin prepared from SH-SY5Ycells treated with 16 nM PMA for 72 hours (1e6 cell equivalents per IP) were subjected to chromatin immunoprecipitation using 8 µg of either Normal Chicken IgY with bridging antibody (Part No. CS207346), or 8 µg Anti-MeCP2 with bridging antibody (Part No. CS207345) and the Magna ChIP HiSens (Cat. # 17-10460). Successful immunoprecipitation of MeCP2 associated DNA fragments was verified by qPCR using ChIP Primers, human SNRPN (Part No. CS207347) as a positive locus, and GAPDH promoter primers (Part #22-004) as a negative locus. Please refer to the Magna ChIP HiSens (Cat. # 17-10460) or EZ-MagnaChIP HiSens(Cat. # 17-10461) protocol for experimental details. (Cat. # 17-10460) or EZ-MagnaChIP HiSens(Cat. # 17-10461) protocol for experimental details.
Chromatin Immunoprecipitation Analysis:
A representative lot of this antibody was used by an independent laboratory in ChIP. (Thatcher, K., et al. (2005). Hum. Mol. Genet. 14(6): 785-797.)
Immunoprecipitation Analysis:
A representative lot was used by an independent laboratory in IP. (Thatcher, K., et al. (2005). Hum. Mol. Genet. 14(6): 785-797.)
Western Blotting Analysis:
1 µg/mL of this antibody (prior to blending with rabbit anti-chicken bridging antibody) detected MeCp2 on 10 µg of SH-SY5Y nuclear extract.
Important Note: For western blot application of the blended antibody, use 1:680 dilution in combination with anti-rabbit HRP secondary.
Epigenetics & Nuclear Function
Chromatin Biology
Packaging
Physical form
Normal Chicken IgY/Rabbit Blend, Part No. CS207346. One vial containing 200 μg of purified chicken IgY blended with purified rabbit anti-chicken IgG in 145 μL storage buffer containing 0.05% sodium azide and 30% glycerol (1.38 mg/ml final, use 5.8 µL per ChIP) . Store at -20°C.
ChIP Primers, SNRPN. Part No. CS207347. One vial containing 75 μL of 5 μM of each primer specific for a human SNRPN intron region (chr15:25200483-25200626, hg19 build). Store at -20°C.
FOR: TAC CTC CGC CTA AAA TCC CTA TG
REV: GGA AGG GCG GTG GTG ACT
Preparation Note
Analysis Note
Sonicated chromatin prepared from SH-SY5Y cells treated with 16 nM PMA for 72 hours (1e6 cell equivalents per IP) were subjected to chromatin immunoprecipitation using 8 µg of either Normal Chicken IgY with bridging antibody (Part No. CS207346), or 8 µg Anti-MeCP2 with bridging antibody (Part No. CS207345) and the Magna ChIP® HiSens Kit (Cat. # 17-10460). Successful immunoprecipitation of MeCP2 associated DNA fragments was verified by qPCR using ChIP Primers, human SNRPN (Part No. CS207347).
Please refer to the MagnaChIP HiSens (Cat. # 17-10460) or EZ-MagnaChIP HiSens (Cat. # 17-10461) protocol for experimental details.
Includes normal chicken IgY/rabbit IgG and primers specific for a human SNRPN intron region.
Other Notes
Legal Information
Disclaimer
Storage Class Code
10 - Combustible liquids
Certificates of Analysis (COA)
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Related Content
Epigenetics describes heritable changes in gene expression caused by non-genetic mechanisms. Epigenetic regulation allows a cell to vary its response based on its biological and environmental contexts. Epigenetic changes can effect transcriptional and post-transcriptional regulation via mechanisms such as histone modification, chromatin and nucleosome remodeling, DNA methylation, and small and non-coding RNA-mediated regulation. These mechanisms, in cooperation with transcription factors and other nucleic acid-binding proteins, regulate gene expression. Epigenetic mechanisms of gene regulation impacts diverse areas of research—from agriculture to human health. Common epigenetic assays such as chromatin immunoprecipitation (ChIP) and RNA immunoprecipitation (RIP) rely on high quality antibodies that recognize specific epigenetic modifications for accurate results. EMD Millipore offers over 100 ChIPAb+™ and RIPAb+™ validated antibody kits that are quality tested on ChIP/RIP assays and are conveniently provided with control qPCR primers and negative control antibodies to ensure first time ChIP/RIP success.
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