sgrna expression vectors lrg Search Results


sgrna expression vectors lrg  (Addgene inc)
95
Addgene inc sgrna expression vectors lrg
Sgrna Expression Vectors Lrg, supplied by Addgene inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sgrna+expression+vectors+lrg/LRG+(Lenti_sgRNA_EFS_GFP)+(Plasmid+%2365656)/pmc11260449-49-7-11
Average 95 stars, based on 1 article reviews
sgrna expression vectors lrg - by Bioz Stars, 2026-10
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lentiviral single guide rna sgrna expression vectors  (Addgene inc)
94
Addgene inc lentiviral single guide rna sgrna expression vectors
SIK3 and MEF2C are selectively essential for the growth of AML and multiple myeloma cells. (A) SIK3 and MEF2C essentiality scores extracted from the DepMap database of cancer cell lines.35 Shown is a boxplot distribution of the copy number–adjusted essentiality score (CERES; a normalized metric of gene essentiality) of SIK3 and MEF2C across all 558 cell lines, 16 AML lines, 18 multiple myeloma lines, and 498 solid tumor cell lines. (B-C) Scatterplots of SIK3 and MEF2C essentiality scores in human AML cell lines in the DepMap (CERES) or from Wang et al52 (CRISPR scores). (D) Western blot analysis of MEF2C in RN2 and 3T3 whole-cell lysates. (E) Competition-based proliferation assays in which cells were infected with the indicated sgRNAs linked to GFP. Bar graphs represent the mean ± standard error of the mean (SEM; n = 3). (F) Bright-field images of methylcellulose-based colony-formation assays of normal myeloid progenitors or RN2 cells on day 7 after retroviral transduction with control or Sik3 shRNAs. (G) Quantification of the immature/blast colonies shown in panel F. Mean ± SEM (n = 4). (H) Western blot analysis of SIK3 performed on day 6 after infection of the indicated shRNAs. (I) Bioluminescence imaging of wild-type C57BL/6 mice receiving transplants of Cas9-expressing RN2 cells transduced with the indicated <t>sgRNA.</t> Representative images are shown on the indicated day after transplantation. (J) Quantification of bioluminescence from panel I. Values represent photons per second (p/s) of bioluminescent signal detection (mean ± SEM). The P value was calculated by unpaired Student t test (n = 5). (K) Survival curves of the mice in panel I. The P value was calculated by log-rank (Mantel-Cox) test (n = 5). (L) Bioluminescence imaging of NSG (NOD-SCID/IL2Rgammanull) mice which received transplants of Cas9-expressing MV4-11 cells transduced with the indicated sgRNA. Representative images are shown on the indicated day after transplantation. (M) Quantification of bioluminescence from panel L. Values represent photons per second (p/s) of bioluminescent signal detection (mean ± SEM). The P value was calculated by unpaired Student t test (n = 5). (N) Survival curves of the mice in panel L. The P value was calculated by log-rank (Mantel-Cox) test (n = 5). sgNeg1, sgNeg2, shREN: negative controls. sgRpa3: positive control.
Lentiviral Single Guide Rna Sgrna Expression Vectors, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sgrna+expression+vectors+lrg/LRG2%2E1+(Plasmid+%23108098)/pmc06940199-44-3-10
Average 94 stars, based on 1 article reviews
lentiviral single guide rna sgrna expression vectors - by Bioz Stars, 2026-10
94/100 stars
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sgrna/cas9 all-in-one expression clones targeting klrg2  (Genecopoeia)
N/A
Transfect cells with our CRISPR plasmids with Cas9 and sgRNA for human, mouse, and rat. Search our database of more than 45,000 human, mouse, and rat genes for genome editing using CRISPR. sgRNA expression plasmids
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sgrna/cas9 all-in-one expression clones targeting lrguk  (Genecopoeia)
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Transfect cells with our CRISPR plasmids with Cas9 and sgRNA for human, mouse, and rat. Search our database of more than 45,000 human, mouse, and rat genes for genome editing using CRISPR. sgRNA expression plasmids
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sgrna/cas9 all-in-one expression clones targeting lrg1  (Genecopoeia)
N/A
Transfect cells with our CRISPR plasmids with Cas9 and sgRNA for human, mouse, and rat. Search our database of more than 45,000 human, mouse, and rat genes for genome editing using CRISPR. sgRNA expression plasmids
   Buy from Supplier
sgrna/cas9 all-in-one expression clones targeting klrg1  (Genecopoeia)
N/A
Transfect cells with our CRISPR plasmids with Cas9 and sgRNA for human, mouse, and rat. Search our database of more than 45,000 human, mouse, and rat genes for genome editing using CRISPR. sgRNA expression plasmids
   Buy from Supplier
sgrna/cas9 all-in-one expression clones targeting plrg1  (Genecopoeia)
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Transfect cells with our CRISPR plasmids with Cas9 and sgRNA for human, mouse, and rat. Search our database of more than 45,000 human, mouse, and rat genes for genome editing using CRISPR. sgRNA expression plasmids
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Image Search Results


SIK3 and MEF2C are selectively essential for the growth of AML and multiple myeloma cells. (A) SIK3 and MEF2C essentiality scores extracted from the DepMap database of cancer cell lines.35 Shown is a boxplot distribution of the copy number–adjusted essentiality score (CERES; a normalized metric of gene essentiality) of SIK3 and MEF2C across all 558 cell lines, 16 AML lines, 18 multiple myeloma lines, and 498 solid tumor cell lines. (B-C) Scatterplots of SIK3 and MEF2C essentiality scores in human AML cell lines in the DepMap (CERES) or from Wang et al52 (CRISPR scores). (D) Western blot analysis of MEF2C in RN2 and 3T3 whole-cell lysates. (E) Competition-based proliferation assays in which cells were infected with the indicated sgRNAs linked to GFP. Bar graphs represent the mean ± standard error of the mean (SEM; n = 3). (F) Bright-field images of methylcellulose-based colony-formation assays of normal myeloid progenitors or RN2 cells on day 7 after retroviral transduction with control or Sik3 shRNAs. (G) Quantification of the immature/blast colonies shown in panel F. Mean ± SEM (n = 4). (H) Western blot analysis of SIK3 performed on day 6 after infection of the indicated shRNAs. (I) Bioluminescence imaging of wild-type C57BL/6 mice receiving transplants of Cas9-expressing RN2 cells transduced with the indicated sgRNA. Representative images are shown on the indicated day after transplantation. (J) Quantification of bioluminescence from panel I. Values represent photons per second (p/s) of bioluminescent signal detection (mean ± SEM). The P value was calculated by unpaired Student t test (n = 5). (K) Survival curves of the mice in panel I. The P value was calculated by log-rank (Mantel-Cox) test (n = 5). (L) Bioluminescence imaging of NSG (NOD-SCID/IL2Rgammanull) mice which received transplants of Cas9-expressing MV4-11 cells transduced with the indicated sgRNA. Representative images are shown on the indicated day after transplantation. (M) Quantification of bioluminescence from panel L. Values represent photons per second (p/s) of bioluminescent signal detection (mean ± SEM). The P value was calculated by unpaired Student t test (n = 5). (N) Survival curves of the mice in panel L. The P value was calculated by log-rank (Mantel-Cox) test (n = 5). sgNeg1, sgNeg2, shREN: negative controls. sgRpa3: positive control.

Journal: Blood

Article Title: Salt-inducible kinase inhibition suppresses acute myeloid leukemia progression in vivo

doi: 10.1182/blood.2019001576

Figure Lengend Snippet: SIK3 and MEF2C are selectively essential for the growth of AML and multiple myeloma cells. (A) SIK3 and MEF2C essentiality scores extracted from the DepMap database of cancer cell lines.35 Shown is a boxplot distribution of the copy number–adjusted essentiality score (CERES; a normalized metric of gene essentiality) of SIK3 and MEF2C across all 558 cell lines, 16 AML lines, 18 multiple myeloma lines, and 498 solid tumor cell lines. (B-C) Scatterplots of SIK3 and MEF2C essentiality scores in human AML cell lines in the DepMap (CERES) or from Wang et al52 (CRISPR scores). (D) Western blot analysis of MEF2C in RN2 and 3T3 whole-cell lysates. (E) Competition-based proliferation assays in which cells were infected with the indicated sgRNAs linked to GFP. Bar graphs represent the mean ± standard error of the mean (SEM; n = 3). (F) Bright-field images of methylcellulose-based colony-formation assays of normal myeloid progenitors or RN2 cells on day 7 after retroviral transduction with control or Sik3 shRNAs. (G) Quantification of the immature/blast colonies shown in panel F. Mean ± SEM (n = 4). (H) Western blot analysis of SIK3 performed on day 6 after infection of the indicated shRNAs. (I) Bioluminescence imaging of wild-type C57BL/6 mice receiving transplants of Cas9-expressing RN2 cells transduced with the indicated sgRNA. Representative images are shown on the indicated day after transplantation. (J) Quantification of bioluminescence from panel I. Values represent photons per second (p/s) of bioluminescent signal detection (mean ± SEM). The P value was calculated by unpaired Student t test (n = 5). (K) Survival curves of the mice in panel I. The P value was calculated by log-rank (Mantel-Cox) test (n = 5). (L) Bioluminescence imaging of NSG (NOD-SCID/IL2Rgammanull) mice which received transplants of Cas9-expressing MV4-11 cells transduced with the indicated sgRNA. Representative images are shown on the indicated day after transplantation. (M) Quantification of bioluminescence from panel L. Values represent photons per second (p/s) of bioluminescent signal detection (mean ± SEM). The P value was calculated by unpaired Student t test (n = 5). (N) Survival curves of the mice in panel L. The P value was calculated by log-rank (Mantel-Cox) test (n = 5). sgNeg1, sgNeg2, shREN: negative controls. sgRpa3: positive control.

Article Snippet: Plasmid constructions The lentiviral single-guide RNA (sgRNA) expression vectors (LRG2.1, Addgene_108098; LRG, Addgene_65656) and the lentiviral Cas9 (LentiV_Cas9_puro, Addgene_108100) or luciferase (Lenti-luciferase-P2A-Neo, Addgene_105621) expression vectors were described previously.

Techniques: CRISPR, Western Blot, Infection, Retroviral, Transduction, Control, Imaging, Expressing, Transplantation Assay, Positive Control