resampling bootstrap approach sas multtest Search Results


multtest package  (RStudio)
90
RStudio multtest package
Multtest Package, supplied by RStudio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/resampling+bootstrap+approach+sas+multtest/multtest+package/pmc07906474-160-20-6
Average 90 stars, based on 1 article reviews
multtest package - by Bioz Stars, 2026-10
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multtest antibody cocktail (anti-cd3/cd16+cd56/cd45/cd19  (Becton Dickinson)
90
Becton Dickinson multtest antibody cocktail (anti-cd3/cd16+cd56/cd45/cd19
Lysis of K562 and K562.ΔCprME-PAC2A cells by the primary NK line and NK clones. (A) Reduced cytotoxic activity of the primary NK line against K562 cells expressing the DV replicon. Primary NK cells prepared as described in Materials and Methods were incubated for 5 hours with labeled K562 and K562.ΔCprME-PAC2A cells. Results are from one representative experiment out of two performed. The value for each time point is the mean of the percent specific lysis of four separate wells. *, P < 0.04, as analyzed by single-factor analysis of variance. (B and C) NK clone lysis against K562 and K562.ΔCprME-PAC2A cells. Clones were stained for the presence of KIR2DL1 and KIR2DL2 receptors using anti-KIR2DL1 and anti-KIR2DL2 MAbs. (B) Lysis of K562 and K562.ΔCprME-PAC2A cells by two representative NK clones expressing only KIR2DL2 (AB3) or both KIR2DL1 and KIR2DL2 (AB2). (C) Lysis of K562 and K562.ΔCprME-PAC2A cells by two representative NK clones <t>(CD3</t> and EF9) that don't express either KIR2DL1 or KIR2DL2. Results for all the lysis assays presented are from one representative experiment out of two performed. The value for each time point is the mean of the percent specific lysis of four separate wells.
Multtest Antibody Cocktail (Anti Cd3/Cd16+Cd56/Cd45/Cd19, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/resampling+bootstrap+approach+sas+multtest/anti+cd56/pmc02493327-42-6-5
Average 90 stars, based on 1 article reviews
multtest antibody cocktail (anti-cd3/cd16+cd56/cd45/cd19 - by Bioz Stars, 2026-10
90/100 stars
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textural analyzer  (Food Technology Corporation)
86
Food Technology Corporation textural analyzer
Lysis of K562 and K562.ΔCprME-PAC2A cells by the primary NK line and NK clones. (A) Reduced cytotoxic activity of the primary NK line against K562 cells expressing the DV replicon. Primary NK cells prepared as described in Materials and Methods were incubated for 5 hours with labeled K562 and K562.ΔCprME-PAC2A cells. Results are from one representative experiment out of two performed. The value for each time point is the mean of the percent specific lysis of four separate wells. *, P < 0.04, as analyzed by single-factor analysis of variance. (B and C) NK clone lysis against K562 and K562.ΔCprME-PAC2A cells. Clones were stained for the presence of KIR2DL1 and KIR2DL2 receptors using anti-KIR2DL1 and anti-KIR2DL2 MAbs. (B) Lysis of K562 and K562.ΔCprME-PAC2A cells by two representative NK clones expressing only KIR2DL2 (AB3) or both KIR2DL1 and KIR2DL2 (AB2). (C) Lysis of K562 and K562.ΔCprME-PAC2A cells by two representative NK clones <t>(CD3</t> and EF9) that don't express either KIR2DL1 or KIR2DL2. Results for all the lysis assays presented are from one representative experiment out of two performed. The value for each time point is the mean of the percent specific lysis of four separate wells.
Textural Analyzer, supplied by Food Technology Corporation, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/resampling+bootstrap+approach+sas+multtest/analyzer+textural/10__1016_slash_j__jfutfo__2025__03__013-208-11-15
Average 86 stars, based on 1 article reviews
textural analyzer - by Bioz Stars, 2026-10
86/100 stars
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Image Search Results


Lysis of K562 and K562.ΔCprME-PAC2A cells by the primary NK line and NK clones. (A) Reduced cytotoxic activity of the primary NK line against K562 cells expressing the DV replicon. Primary NK cells prepared as described in Materials and Methods were incubated for 5 hours with labeled K562 and K562.ΔCprME-PAC2A cells. Results are from one representative experiment out of two performed. The value for each time point is the mean of the percent specific lysis of four separate wells. *, P < 0.04, as analyzed by single-factor analysis of variance. (B and C) NK clone lysis against K562 and K562.ΔCprME-PAC2A cells. Clones were stained for the presence of KIR2DL1 and KIR2DL2 receptors using anti-KIR2DL1 and anti-KIR2DL2 MAbs. (B) Lysis of K562 and K562.ΔCprME-PAC2A cells by two representative NK clones expressing only KIR2DL2 (AB3) or both KIR2DL1 and KIR2DL2 (AB2). (C) Lysis of K562 and K562.ΔCprME-PAC2A cells by two representative NK clones (CD3 and EF9) that don't express either KIR2DL1 or KIR2DL2. Results for all the lysis assays presented are from one representative experiment out of two performed. The value for each time point is the mean of the percent specific lysis of four separate wells.

Journal:

Article Title: Dengue Virus Replicon Expressing the Nonstructural Proteins Suffices To Enhance Membrane Expression of HLA Class I and Inhibit Lysis by Human NK Cells ▿

doi: 10.1128/JVI.02274-07

Figure Lengend Snippet: Lysis of K562 and K562.ΔCprME-PAC2A cells by the primary NK line and NK clones. (A) Reduced cytotoxic activity of the primary NK line against K562 cells expressing the DV replicon. Primary NK cells prepared as described in Materials and Methods were incubated for 5 hours with labeled K562 and K562.ΔCprME-PAC2A cells. Results are from one representative experiment out of two performed. The value for each time point is the mean of the percent specific lysis of four separate wells. *, P < 0.04, as analyzed by single-factor analysis of variance. (B and C) NK clone lysis against K562 and K562.ΔCprME-PAC2A cells. Clones were stained for the presence of KIR2DL1 and KIR2DL2 receptors using anti-KIR2DL1 and anti-KIR2DL2 MAbs. (B) Lysis of K562 and K562.ΔCprME-PAC2A cells by two representative NK clones expressing only KIR2DL2 (AB3) or both KIR2DL1 and KIR2DL2 (AB2). (C) Lysis of K562 and K562.ΔCprME-PAC2A cells by two representative NK clones (CD3 and EF9) that don't express either KIR2DL1 or KIR2DL2. Results for all the lysis assays presented are from one representative experiment out of two performed. The value for each time point is the mean of the percent specific lysis of four separate wells.

Article Snippet: NK purity was assayed using BD Multtest antibody cocktail (anti-CD3/CD16+CD56/CD45/CD19).

Techniques: Lysis, Clone Assay, Activity Assay, Expressing, Incubation, Labeling, Staining