Examples of 'b-gal' in a sentence
Meaning of "b-gal"
b-gal (adjective) - relating to beta-galactosidase enzyme used in molecular biology
How to use "b-gal" in a sentence
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b-gal
Application of b-Gal is in the treatment of milk products.
All injected animals displayed a high level of b-gal activity.
B-gal activity was determined for each cell lysate.
Cells treated with this construct demonstrate b-gal activity.
B-gal activity was present in the airway epithelial cells of exposed rats.
The expression amount of the B-Gal in control clones is varied with each clone.
B-gal activity was determined and the relative transduction efficiency compared.
All binding domain constructs were also tested for self-activation of B-Gal activity.
Expression of the B-Gal gene is used to screen for recombinant vaccinia virus.
The activity of luciferase and B-gal were measured.
A B-Gal gene fragment was cut from pLMBL using restriction enzymes BlnI and BglII.
Shortly after injection many of the b-gal positive cells exhibited a morphology typical of microglial cells.
B-gal positive cultures were subcloned twice and the subclones were used for further studies.
Cells were analysed for B-gal or luciferase expression after two days.
B-gal assays can be performed to quantify binding between identified aptamers and the target.
See also
No significant increase in B-gal units was detected from the groE promoter.
A B-Gal gene fragment was cut from pZeo / lacZ using restriction enzymes PstI and XhoI.
This represents the level of B-gal complementation attributable to the a-fragment alone.
B-Gal contains abundant free sulfhydryl groups in its native state.
The cells were stained for B-gal activity following the procedure of Chiorini et al.
In this study we tested the influence of environmental conditions on the level of B-gal.
PCMV B-Gal was transfected for control of transfectional efficiency.
Cell viability could be determined by inspection under a microscope, or by monitoring B-gal activity.
Inhibition of B-Gal expression was determined by measuring the B-galactosidase activity.
The transfection efficiency was evaluated using B-gal stain or an enzyme activity assay.
The presence of B-gal activity was determined using a standard histochemical staining procedure.
Cells were restimulated in vitro during a 4 day incubation with different concentrations of soluble B-gal.
Conjugation of B-Gal with SMCC alone did not enhance uptake.
Addition of doxycycline resulted in a 4 fold increase in the amount of B-gal produced over background.
Enzymatic activity of B-gal was observed in a large number of macrophage like cells.
Following fusión of the two cell lines Tat induce the expression of B-gal enzyme.
In control grafts B-gal plasmid was used in sterile water mixed with thrombin.
Six days later the brains of both animals were fixed and processed for B-gal histochemistry.
No B-gal activity was detected in both transient and stable insect cell lines.
The process enabled high retention of B-gal activity, comparable to its aqueous activity.
The B-gal reporter gene was used to assess the transfection efficiency on a per cell basis.
Splenocytes were cultured and stimulated with NP or B-gal protein.
The coding region of B-gal also serves as a genotypic marker of the recombinant virus.
Positive hybridomas were identified by ELISA using B-gal adsorbed to plastic plates.
The cells were stained for B-gal activity and the relative transduction efficiency compared.
LUC activity was measured and normalized for transfection efficiency by B-gal activity.
The level of B-gal activity following infection represents a measure of the infectivity of the virus.
The histologic consequencies of VEGF and B-gal transfection were studied at 2 weeks.
The B-gal activity was detected as described in Material and Methods.
Similar results were obtained in a second assay for both NP and B-gal specific CTL.
Reaction mixes were processed for B-gal production using the B-gal reporter gene assay.
Skin is harvested 48 h after transfection and processed for b-gal activity.
Without the TAT Peptide B-Gal was not observed in the CNS.
In contrast, INFg producing cells were scarcely detectable after i . n . administration of B-Gal.
The coding region for B-gal is deleted from pCMVb by the Not I digestion.
