Examples of 'immunoblots' in a sentence
Meaning of "immunoblots"
immunoblots (noun) - Immunoblots are laboratory techniques used to detect specific proteins in a sample using antibodies. This method involves separating proteins by gel electrophoresis and then transferring them to a membrane for antibody detection. Immunoblots are commonly used in biochemistry and molecular biology research for protein analysis and detection.
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- plural of immunoblot
How to use "immunoblots" in a sentence
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immunoblots
The analysis is confirmed by immunoblots in representative studies.
Immunoblots were probed with appropriate antiphosphotyrosine antibody.
Subsequent normalization and immunoblots were performed as above.
Immunoblots of various FVa and FVai mutants.
All isoelectric forms were recognized on immunoblots by the antiserum.
Immunoblots were quantified and normalized to calsequestrin expression.
Data were quantified and shown as graphs below the immunoblots.
The immunoblots were visualized by enhanced chemiluminescence.
Immunoprecipitation and antiphosphotyrosine immunoblots.
The immunoblots were treated and processed.
They all also showed moderate to strong reactivity in immunoblots.
Immunoblots were developed by a nitro blue tetrasodium salt stain.
Unorthodox applications of immunoblots.
It shows immunoblots produced on gel.
This affinity purified antibody reacted with the partially purified protein on immunoblots.
See also
The immunoblots were autoradiographed to identify the human lactoferrin protein.
Equal loading was monitored by immunoblots for actin and at least one additional protein.
Immunoblots demonstrating the expression of chromosomally integrated antigen cassettes.
It has not been possible to detect a corresponding component reacting with the antibodies on immunoblots.
Immunoblots for each panel are representative of three independent experiments.
Labeled cell lysates were analyzed on immunoblots Fig.
Betaactin immunoblots served as control.
The ER levels was quantitated by densitometry of immunoblots.
Immunoblots were incubated with the appropriate antibodies as indicated in figure legends.
Densitometric analyses of the immunoblots of Figs.
Immunoblots were performed as above.
The ER levels were quantitated by densitometry of immunoblots.
Immunoblots confirm that the receptor protein band is absent in this mutant.
All samples were then treated with PK and analyzed by immunoblots.
Immunoblots were probed with antibodies specific for the proteins indicated on the left.
Both proteins reacted with antibodies specific for FVII on immunoblots.
TBRF ImmunoBlots IgM and IgG.
Additionally preferred assays for analyzing the present polyspecific binding proteins include Western immunoblots.
Immunoblots showed that cell surface CRT increased upon Btk activation and decreased upon Btk inhibition.
The positions of Alanine mutants are indicated above the Immunoblots.
Immunoblots were developed using an anti-FKBP antibody.
Shown are representative immunoblots from 3 similar experiments.
Immunoblots were detected using mouse monoclonal anti-FLAG antibodies.
In order to confirm the results, immunoblots were performed.
B-actin immunoblots are presented as equal loading control.
Simultaneously, the same serum samples were tested on immunoblots with eukaryotic nuclear proteins as antigen.
The immunoblots revealed enhanced levels of AChE-R in samples of stressed patients.
Quantitation of ABCG2 expression was achieved by densitometry of the immunoblots.
Fractions were collected and immunoblots were performed on ethanol-precipitated proteins.
Immunoblots were immersed in substrate for 5 min and subsequently exposed to film for 1s.
With specific regard to Figure 6, there is seen immunoblots prepared from other Pseudomonas syringae strains.
On immunoblots with polyclonal antibodies raised against PhtD, we could detect PhtD in all strains.
Cells were lysed 15 min after VEGF addition and immunoblots were probed with the indicated antibodies.
Immunoblots with adult worm microsomal antigens are species-specific, so a positive reaction indicates the infecting species.
Further, collagens I and III showed the expected molecular weight distributions on immunoblots.
