HIF - 1 alpha was
immunoprecipitated using 0.5 mg HeLa Nuclear DFO treated whole cell extract (ab180880), 5 µg of Mouse monoclonal to HIF - 1 alpha and 50 µl of protein G magnetic beads (+).
HIF -1-alpha was
immunoprecipitated using 0.5 mg HeLa Nuclear DFO treated whole cell extract (ab180880), 5µg of Rabbit polyclonal to HIF1 alpha and 50µl of protein G magnetic beads (+).
Not exact matches
Nagaki et al. [6]
used anti-CenH3 antibodies to
immunoprecipitate chromatin (ChIP) comprising DNA bound to CenH3 - containing nucleosomes, confirming that CenH3 is associated with both the CentO repeats and the CRR family of retrotransposons.
Unpurified ab32518
used to
immunoprecipitate IKB alpha from human HeLa whole cell lysate.
Unpurified ab32518
used to
immunoprecipitate IKB alpha from rat PC12 whole cell lysate.
After extensive washing with immunoprecipitation lysis buffer, the
immunoprecipitated proteins were analyzed by immunoblotting
using specific antibodies against DDX3 and FLAG epitope (ab1257, Abcam, Cambridge, United Kingdom).
Tip 6: For detection of
immunoprecipitated proteins by Western blotting, without or reduced detection of non-specific artifacts (such as the heavy and light chains of the
immunoprecipitating antibody), detect primary antibodies
using HRP - conjugated anti-rabbit light chain - specific (L) antibody and HRP - conjugated Protein A instead of traditional HRP - conjugated secondary antibodies.
It will make
use of cutting - edge approaches in vivo and in vitro, including mouse genetic models and next - generation sequencing of RNA and
immunoprecipitated chromatin (RNA - seq and ChIP - seq).
The
immunoprecipitated chromatin by anti — IRF - 9 antibody was analyzed by PCR
using primers specific for RIG - G promoter sequences (+11 to − 288).
For this protocol, samples were lysed in 1 × RIPK2 lysis buffer [50 mM Tris (pH 7.5), 0 mM MgCl2, 1 % Triton X-100, 1 mM dithiothreitol, 1 mM EDTA, 1 mM EGTA, with freshly added 1 mM β - glycerophosphate and protease inhibitors (phenylmethylsulfonyl fluoride and aprotinin)-RSB- and
immunoprecipitated overnight
using 1.5 μg rabbit anti-RIPK2 antibody.
METHODS: We treated 3T3 - L1 adipocytes with 2.5 mmol / l R (+) alpha - lipoic acid for 2 to 60 min, followed by assays of: 2 - deoxyglucose uptake; glucose transporter 1 and 4 (GLUT1 and GLUT4) subcellular localization; tyrosine phosphorylation of the insulin receptor or of the insulin receptor substrate - 1 in cell lysates; association of phosphatidylinositol 3 - kinase activity with
immunoprecipitates of proteins containing phosphotyrosine or of insulin receptor substrate - 1
using a in vitro kinase assay; association of the p85 subunit of phosphatidylinositol 3 - kinase with phosphotyrosine proteins or with insulin receptor substrate - 1; and in vitro activity of
immunoprecipitated Akt1.
When an antibody to endogenous SUV39H1 was
used for immunoprecipitation, MeCP2 was effectively coimmunoprecipitated; conversely, aHA antibodies to HA - tagged MeCP2 could
immunoprecipitate SUV39H1 (Fig. 2G).»