anti br utp mab (Millipore)
Name:
Monoclonal Anti hnRNP K J antibody
Description:
Monoclonal Anti hnRNP K J mouse IgG2b isotype is derived from the 3C2 hybridoma produced by the fusion of mouse myeloma cells SP2 0 cells and splenocytes from BALB c mice immunized with hnRNP s purified by oligo dC affinity chromatography
Catalog Number:
r8903
Price:
None
Applications:
The antibody may be used in various immunochemical techniques including enzyme linked immunosorbent assay (ELISA), immunoblotting, chromatin immunoprecipitation (ChIP), immunocytochemistry, antibody-based supershift assay and electrophoretic mobility shift assay (EMSA).
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Structured Review

Monoclonal Anti hnRNP K J mouse IgG2b isotype is derived from the 3C2 hybridoma produced by the fusion of mouse myeloma cells SP2 0 cells and splenocytes from BALB c mice immunized with hnRNP s purified by oligo dC affinity chromatography
https://www.bioz.com/result/anti br utp mab/product/Millipore
Average 85 stars, based on 1 article reviews
Price from $9.99 to $1999.99
Images
1) Product Images from "Initiation of Nucleolar Assembly Is Independent of RNA Polymerase I Transcription"
Article Title: Initiation of Nucleolar Assembly Is Independent of RNA Polymerase I Transcription
Journal: Molecular Biology of the Cell
doi:

Figure Legend Snippet: ActD at a concentration of 0.04 μg/ml selectively inhibits Pol I transcription without significantly affecting other polymerases and general nuclear organization. A and A′ show the in situ incorporation of Br-UTP, and B and B′ show the same cells corresponding to those in A and A′ immunolabeled with anti-fibrillarin antibody. Daughter cells grown in the presence of ActD form mininucleoli that are immunolabeled with anti-fibrillarin antibody (B, arrows). They do not incorporate Br-UTP (A, arrows), whereas untreated nucleoli (B′, arrows) actively incorporate Br-UTP after pulse labeling (A′). Although Br-UTP incorporation in nucleoli declines in treated cells, the nucleoplasmic Br-UTP incorporation from Pol II and Pol III transcription is not altered (A). The speckled distribution of SC35 (C) and the predominantly nuclear localization of hnRNP A1 (D) are also not changed significantly in treated cells. Bar, 10 μm.
Techniques Used: Concentration Assay, In Situ, Immunolabeling, Labeling
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