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The reaction products were analyzed by Western analysis using an anti-WRN antibody.
Knock down of MUC1 protein was evaluated by Western analysis using Anti-MUC1* antibody.
Confirmation of this identification was performed by Western analysis using an anti-CaMKKα antibody (Figure 1B).
Corresponding TXNL6 protein levels were also analyzed by western analysis using a TXNL6-specific antibody.
Immunoisolated proteins were detected by Western analysis using anti-GFP antibodies and quantified using the QuantityOne software (Bio-Rad).
TXNL6 transcripts were monitored by RT-PCR and TXNL6 protein examined by western analysis using a TXNL6-specific antibody.
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Next, we tested whether these cells displayed lower expression of Hsp27 by performing western analysis using anti-Hsp27 antibody.
Samples were separated by SDS PAGE followed by western blot analysis using the appropriated antibodies.
We also probed IP3R isoform-expression levels by qRT-PCR and by western blot analysis using isoform-specific antibodies.
The cellular OsUbc13 was detected by western bolt analysis using the anti-hUbc13 mAb 4E11 (Andersen et al. [2005]).
Production of membrane-displayed somatostatin on yeast plasma membranes was confirmed by western blot analysis using anti-FLAG tag antibody.
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by multivariate analysis using
by densitometry analysis using
by phylogenic analysis using
by numerical analysis using
by bioinformatic analysis using
by corresponding analysis using
by noncompartmental analysis using
by statistical analysis using
by quantitative analysis using
by elemental analysis using
by densitometric analysis using
by biochemical analysis using
by Probit analysis using
by morphodensitometric analysis using
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