biological source
mouse
clone
monoclonal
product line
Upstate®
species reactivity
mouse, rabbit, human, Xenopus
technique(s)
immunoprecipitation (IP): suitable (RNA binding protein)
immunoprecipitation (IP): suitable
western blot: suitable
Quality Level
Analysis Note
RIP Lysate prepared from HeLa cells (2 x 107cell equivalents per IP) were subjected to immunoprecipitation using 5 ug of either a normal mouse IgG or the anti-PABPC1 antibody and the Magna RIP Kit (Cat. # 17-700).
Successful immunoprecipitation of PABPC1-associated RNA was verified by qRT-PCR using RIP Primers, ACTB. Please refer to the Magna RIP (Cat. # 17-700) or EZ-Magna RIP (Cat. # 17-701) protocol for experimental details.
Application
Immunoprecipitation from RIP lysate:
RIP lysate from HeLa cells (2 X 106 cell equivalents per IP
General description
The RIPAb+ PABPC1 set includes the PABPC1 antibody, a negative control antibody (purified mouse IgG), and positive qPCR primers which amplify a 100 bp fragment of the human ACTB cDNA. The PABPC1 and negative control antibodies are supplied in a scalable "per RIP" reaction size and can be used to functionally validate the precipitation of PABPC1-associated RNAs.
Immunogen
Other Notes
Legal Information
Storage Class
10 - Combustible liquids
Certificates of Analysis (COA)
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Related Content
All eukaryotic organisms require tight regulation of gene expression for complex processes such as development, differentiation, cell specification, and responses to environmental stimuli. Many genes are regulated post-transcriptionally, in addition to transcriptional mechanisms of gene regulation. RNA-binding proteins (RBPs) are essential for post-transcriptional gene regulation, linking transcription and translation in many processes including transcription, splicing, export, rate of translation and turnover. In all of these events, RBPs coordinate regulation of the amount of protein produced from mRNA transcripts.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 03-101 | 04053252320415 |
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