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Informazioni su questo articolo
Vai a
Origine biologica
mouse
Livello qualitativo
Clone
CMA304, monoclonal
Purificato mediante
using protein G
Reattività contro le specie
human, vertebrates
Produttore/marchio commerciale
ChIPAb+
Upstate®
tecniche
ChIP: suitable (ChIP-seq)
immunocytochemistry: suitable
western blot: suitable
Isotipo
IgG1κ
N° accesso NCBI
Condizioni di spedizione
dry ice
1 of 4
Questo articolo | 17-677 | 17-681 | 17-680 |
|---|---|---|---|
| biological source mouse | biological source mouse | biological source mouse | biological source mouse |
| species reactivity human, vertebrates | species reactivity human, vertebrates | species reactivity human, vertebrates | species reactivity vertebrates, human |
| clone CMA304, monoclonal | clone CMA303, monoclonal | clone CMA307, monoclonal | clone CMA306, monoclonal |
| UniProt accession no. | UniProt accession no. | UniProt accession no. | UniProt accession no. |
| technique(s) ChIP: suitable (ChIP-seq), western blot: suitable, immunocytochemistry: suitable | technique(s) ChIP: suitable (ChIP-seq), dot blot: suitable, multiplexing: suitable, western blot: suitable | technique(s) ChIP: suitable, western blot: suitable | technique(s) ChIP: suitable (ChIP-seq), immunoprecipitation (IP): suitable, western blot: suitable |
| shipped in dry ice | shipped in dry ice | shipped in dry ice | shipped in dry ice |
Descrizione generale
The ChIPAb+ Trimethyl-Histone H3 (Lys4) set includes the Anti-trimethyl-Histone H3 (Lys4) antibody, a negative control antibody (purified Mouse IgG), and qPCR primers which amplify a 166 bp region within the promoter of the human GAPDH gene. The trimethyl-Histone H3 (Lys4) and negative control antibodies are supplied in a scalable "per ChIP" reaction size and can be used to functionally validate the precipitation of trimethyl-histone H3 (Lys4)-associated chromatin.
Immunogeno
Applicazioni
Sonicated chromatin prepared from untreated or colcemid treated HeLa cells (1 X 106 cell equivalents per IP) was subjected to chromatin immunoprecipitation using 2 µg of either a normal mouse IgG or Anti-trimethyl-Histone H3 (Lys4) antibody and the Magna ChIP G Kit (Cat. #17-611). Successful immunoprecipitation of trimethyl-Histone H3 (Lys4) associated DNA fragments was verified by qPCR using primers ampliflying a region of the human B-Globin promoter or using GAPDH promoter Control Primers (Please see figures). Data is presented as percent input of each IP sample relative to input chromatin for each amplicon and ChIP sample as indicated.
Please refer to the EZ-Magna G ChIP (Cat. #17-408) or EZ-ChIP (Cat. #17-371) protocol for experimental details.
Western Blot Analysis:
Representative lot data.
HeLa acid extract were resolved by electrophoresis, transferred to PVDF membrane and probed with Anti-trimethyl Histone H3 (Lys4), clone CMA304 at 1 μg/ml (lane 1) or 0.5 μg/ml (lane 2). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP (Cat. #AP124P) and a chemiluminescence detection system (Please see figures).
Epigenetics & Nuclear Function
Chromatin Biology
Azioni biochim/fisiol
Confezionamento
Stato fisico
Normal Mouse IgG. Two vials containing 25 μg purified mouse IgG in 25 μL storage buffer containing 0.1% sodium azide. Store at -20°C.
Control Primers. One vial containing 75 μL of 5 μM of each primer specific for the promoter region of GAPDH. Store at -20°C.
FOR: TAC TAG CGG TTT TAC GGG CG
REV: TCG AAC AGG AGG AGC AGA GAG CGA
Nota sulla preparazione
Risultati analitici
Sonicated chromatin prepared from colcemid-reated HeLa cells (1 X 106 cell equivalents per IP) were subjected to chromatin immunoprecipitation using 2 µg of either normal mouse IgG or Anti-trimethyl-Histone H3 (Lys4) antibody and the Magna ChIP G Kit (Cat. #17-611). Successful immuno-precipitation of trimethyl-histone H3 (Lys4) associated DNA fragments was verified by qPCR using Control Primers (Please see figures).
Please refer to the EZ-Magna G ChIP (Cat. #17-409) or EZ-ChIP (Cat. #17-371) protocol for experimental details.
Included negative control mouse IgG antibody and control primers specific for human GAPDH promoter.
Note legali
Esclusione di responsabilità
Codice della classe di stoccaggio
10 - Combustible liquids
Certificati d'analisi (COA)
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Signaling Product Guide: Antibodies, small molecule inhibitors, kits, assays and proteins for signaling research.
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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