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Image Search Results
Journal: Cell Metabolism
Article Title: Dynamic Cardiolipin Synthesis Is Required for CD8 + T Cell Immunity
doi: 10.1016/j.cmet.2020.11.003
Figure Lengend Snippet:
Article Snippet: TaqMan Gene expression Assay, Assay ID:
Techniques: Virus, Control, Recombinant, Staining, Isolation, Cell Isolation, Reverse Transcription, Bicinchoninic Acid Protein Assay, Gene Expression, Plasmid Preparation, Software
Journal: Advanced Science
Article Title: Mistranslation Drives Alterations in Protein Levels and the Effects of a Synonymous Variant at the Fibroblast Growth Factor 21 Locus
doi: 10.1002/advs.202004168
Figure Lengend Snippet: RPLP0 abundance determined effects of rs838133 on translation efficiency. a)Multivariate analysis of the tRNA expression patterns using t‐SNE. Three groups of tRNAs (C1, C2, and C3) are highlighted. b)Heatmap of quantification of change in abundance of transcription of 28 tRNA‐associated genes in Huh7 cells stably expressing the A and G alleles of rs838133 of FGF21 analyzed by TaqMan Array and in GEO: GSE32504 and GSE39036, respectively. This showed a unique upregulation in RPLP0 in A allele‐expressing cells c) that was confirmed by RT‐PCR, d) with no changes in other RPLP proteins (RPLP1 and RPLP2). e) The normalized fraction of RPLP0 transcripts associating with actively translating ribosomes was higher in the minor (A) allele compared to the major (G) allele. f) Hierarchical clustering of tRNAs based on their relative changes in abundance upon RPLP0 inhibition by siRNA. RPLP0 inhibition by siRNA decreases FGF21 protein level measured by ELISA g) in cell lysates and h) secreted in medium and i) in active ribosomes in the (A) allele cells restoring it to levels comparable to that in (G) cells. Values of three independent replicates are represented by vertical bars and are mean ± SEM; * p < 0.05 using the student t ‐test or one‐way ANOVA; multiple comparisons were by Bonferroni correction, as appropriate.
Article Snippet: Assay ID:
Techniques: Expressing, Stable Transfection, Reverse Transcription Polymerase Chain Reaction, Inhibition, Enzyme-linked Immunosorbent Assay
Journal: Advanced Science
Article Title: Mistranslation Drives Alterations in Protein Levels and the Effects of a Synonymous Variant at the Fibroblast Growth Factor 21 Locus
doi: 10.1002/advs.202004168
Figure Lengend Snippet: Key resources table
Article Snippet: Assay ID:
Techniques: Virus, Recombinant, Enzyme-linked Immunosorbent Assay, TaqMan SNP Genotyping Assay, Software, Transfection
Journal: Journal of Cellular Biochemistry
Article Title: Targeting PKC-Mediated Signal Transduction Pathways Using Enzastaurin to Promote Apoptosis in Acute Myeloid Leukemia-Derived Cell Lines and Blast Cells
doi: 10.1002/jcb.23090
Figure Lengend Snippet: Patient Characteristics
Article Snippet: Statistical analysis was performed with Sigma Stat computer software (SSPS, Chicago, IL). table ft1 table-wrap mode="anchored" t5 TABLE II caption a7 Common name Symbol Chromosome location ABI assay ID PKC α PRKCA 17q22-q23.2
Techniques:
Journal: Journal of Cellular Biochemistry
Article Title: Targeting PKC-Mediated Signal Transduction Pathways Using Enzastaurin to Promote Apoptosis in Acute Myeloid Leukemia-Derived Cell Lines and Blast Cells
doi: 10.1002/jcb.23090
Figure Lengend Snippet: List of PKC Genes and ABL1 and B2M Control Analyzed Using Real-Time PCR With Applied Biosystems (ABI) Taqman Assays
Article Snippet: Statistical analysis was performed with Sigma Stat computer software (SSPS, Chicago, IL). table ft1 table-wrap mode="anchored" t5 TABLE II caption a7 Common name Symbol Chromosome location ABI assay ID PKC α PRKCA 17q22-q23.2
Techniques: Real-time Polymerase Chain Reaction
Journal: Journal of Cellular Biochemistry
Article Title: Targeting PKC-Mediated Signal Transduction Pathways Using Enzastaurin to Promote Apoptosis in Acute Myeloid Leukemia-Derived Cell Lines and Blast Cells
doi: 10.1002/jcb.23090
Figure Lengend Snippet: PKC β and PKC δ expression is generally elevated IN AML blast cells compared to normal CD34+ bone marrow cells. Real-time PCR was performed as described in Materials and Methods section. Expression of PRKCA (PKC α), PRKCB (PKC β), PRKCD (PKC δ), and PRKCE (PKC ε) genes are presented as relative to 100 copies of b2M for AML-derived cell lines (A) and as relative to 100 copies of ABL1for CD34+ cells derived from bone marrow from normal donors (N = 6) and blast cells derived from AML patients (N = 75; B). P values were derived as described in Materials and Methods section. Statistically significant differences from expression in normal bone marrow cells (P < 0.05) are marked by “*.”
Article Snippet: Statistical analysis was performed with Sigma Stat computer software (SSPS, Chicago, IL). table ft1 table-wrap mode="anchored" t5 TABLE II caption a7 Common name Symbol Chromosome location ABI assay ID PKC α PRKCA 17q22-q23.2
Techniques: Expressing, Real-time Polymerase Chain Reaction, Derivative Assay
Journal: Physiological Genomics
Article Title: Microarray analysis of aging-associated immune system alterations in the rostral ventrolateral medulla of F344 rats
doi: 10.1152/physiolgenomics.00131.2016
Figure Lengend Snippet: List of immune system genes used for quantitative PCR validation of microarray analysis and their TaqMan assay IDs
Article Snippet: Actb, Hprt1, Ldha , and Rplp1 genes were used as endogenous controls and the geometric average of their Ct values was used to calculate each gene’s ΔCt value ( 1 ). table ft1 table-wrap mode="anchored" t5 Table 1. caption a7 Functional Category Gene Symbol TaqMan Assay ID Complement system C1qa
Techniques: Real-time Polymerase Chain Reaction, Biomarker Discovery, Microarray, TaqMan Assay