The phrase "assayed in lysates of" is correct and usable in written English.
It can be used in scientific contexts, particularly in biology or biochemistry, to describe the process of testing or analyzing samples from cell lysates.
Example: "The protein levels were assayed in lysates of various cell types to determine their expression patterns."
Alternatives: "analyzed in lysates of" or "tested in lysates of".
To test this hypothesis, we monitored caspase activation by immunoblot and DEVDase assays in lysates of control and RIPK1-depleted L929sA cells stimulated with brefeldin A, or TNF used as a control.
Glycogen concentration was assayed in muscle lysates by measuring the amount of glucose released after digestion with amyloglucosidase (Aspergillus niger) using a commercial kit (BioVision, Milpitas, CA, USA).
Caspase-3, -8, -9 activities was assayed in LG lysates.
This methodology can be used to assay the total PTPase activity in lysates of various cells and tissues from different sources as well as following treatments with hormones or cytokines.
(F ) Assay of PKA activity in lysates of MEF-derived adipocytes after stimulation with β3-AR-specific agonist CL316243 (CL) or vehicle (veh) in the presence or absence of activin B (Act B).
Therefore we developed a flow cytometric immunobead assay for detection of fusion proteins in lysates of leukemia cell samples by use of a bead-bound catching antibody against one side of the fusion protein and fluorochrome-conjugated detection antibody.
An excellent correlation with standard ELISA assays in cell lysates and sera of cancer patients was obtained.
Thus, VL12.3 binding would be expected to interfere with cleavage at AA 15 and possibly sterically hinder cleavage at AA 8. To determine the effect of compromising cleavage at AA 15 on mHDx-1 clearance, we performed a TR-FRET assay to measure soluble mHDx-1 levels in lysates of organotypic brain slice cultures biolistically transfected with mHDx-1 alone or with either VL12.3 or CVL, a control iAb.
A still unsolved point was that the different purification protocols used failed to recover all of the PARPSso activity assayed in the cell lysate.
We assayed lysates of exfoliated cells in luminal washings from colectomy specimens of 15 patients with colon carcinoma and nine with IBD.
