s17-1 Search Results


e coli s17 1  (ATCC)
95
ATCC e coli s17 1
E Coli S17 1, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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numb overexpression plasmids  (OriGene)
92
OriGene numb overexpression plasmids
Fig. 5 Cell proliferation, migration, and invasion affected by <t>NUMB</t> modulation in melanoma cells. a Cell proliferation assay was performed using RealTime-Glo MT Cell Viability Assay (Promega) in NUMB-overexpressing (NUMB-wild type; S413A-non-phosphorylatable; S413D-phosphomimetic) melanoma cells till 72 h. b Cell migration was analyzed by wound healing assay in NUMB-modulated melanoma cells at 0, 24 and 48 h post-wound creation. c Cell invasion was analyzed by Matrigel invasion chambers using NUMB-modulated melanoma cells at 24 h. The quantitative data are presented as mean ± SEM with statistical significance compared to empty vector (pCMV6) control (**p < 0.01; ***p < 0.001; ****p < 0.0001) or compared to NUMB <t>overexpression</t> (#p < 0.05; ###p < 0.001; ####p < 0.0001 in ≥2 biological replicates with ≥3 technical replicates and 2-3 images per replicate. Scale Bar=400 µm. Statistical significance was determined using one- or two-way ANOVA followed by Fisher’s LSD tests.
Numb Overexpression Plasmids, supplied by OriGene, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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numb overexpression plasmids - by Bioz Stars, 2026-06
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pcmv6 entry plasmid  (OriGene)
90
OriGene pcmv6 entry plasmid
Fig. 5 Cell proliferation, migration, and invasion affected by <t>NUMB</t> modulation in melanoma cells. a Cell proliferation assay was performed using RealTime-Glo MT Cell Viability Assay (Promega) in NUMB-overexpressing (NUMB-wild type; S413A-non-phosphorylatable; S413D-phosphomimetic) melanoma cells till 72 h. b Cell migration was analyzed by wound healing assay in NUMB-modulated melanoma cells at 0, 24 and 48 h post-wound creation. c Cell invasion was analyzed by Matrigel invasion chambers using NUMB-modulated melanoma cells at 24 h. The quantitative data are presented as mean ± SEM with statistical significance compared to empty vector (pCMV6) control (**p < 0.01; ***p < 0.001; ****p < 0.0001) or compared to NUMB <t>overexpression</t> (#p < 0.05; ###p < 0.001; ####p < 0.0001 in ≥2 biological replicates with ≥3 technical replicates and 2-3 images per replicate. Scale Bar=400 µm. Statistical significance was determined using one- or two-way ANOVA followed by Fisher’s LSD tests.
Pcmv6 Entry Plasmid, supplied by OriGene, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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pcmv6 entry plasmid - by Bioz Stars, 2026-06
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icc if proteintech 60137 1 ig cpt1b rabbit  (Proteintech)
93
Proteintech icc if proteintech 60137 1 ig cpt1b rabbit
Fig. 5 Cell proliferation, migration, and invasion affected by <t>NUMB</t> modulation in melanoma cells. a Cell proliferation assay was performed using RealTime-Glo MT Cell Viability Assay (Promega) in NUMB-overexpressing (NUMB-wild type; S413A-non-phosphorylatable; S413D-phosphomimetic) melanoma cells till 72 h. b Cell migration was analyzed by wound healing assay in NUMB-modulated melanoma cells at 0, 24 and 48 h post-wound creation. c Cell invasion was analyzed by Matrigel invasion chambers using NUMB-modulated melanoma cells at 24 h. The quantitative data are presented as mean ± SEM with statistical significance compared to empty vector (pCMV6) control (**p < 0.01; ***p < 0.001; ****p < 0.0001) or compared to NUMB <t>overexpression</t> (#p < 0.05; ###p < 0.001; ####p < 0.0001 in ≥2 biological replicates with ≥3 technical replicates and 2-3 images per replicate. Scale Bar=400 µm. Statistical significance was determined using one- or two-way ANOVA followed by Fisher’s LSD tests.
Icc If Proteintech 60137 1 Ig Cpt1b Rabbit, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
icc if proteintech 60137 1 ig cpt1b rabbit - by Bioz Stars, 2026-06
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origene rg209744  (OriGene)
91
OriGene origene rg209744
Fig. 5 Cell proliferation, migration, and invasion affected by <t>NUMB</t> modulation in melanoma cells. a Cell proliferation assay was performed using RealTime-Glo MT Cell Viability Assay (Promega) in NUMB-overexpressing (NUMB-wild type; S413A-non-phosphorylatable; S413D-phosphomimetic) melanoma cells till 72 h. b Cell migration was analyzed by wound healing assay in NUMB-modulated melanoma cells at 0, 24 and 48 h post-wound creation. c Cell invasion was analyzed by Matrigel invasion chambers using NUMB-modulated melanoma cells at 24 h. The quantitative data are presented as mean ± SEM with statistical significance compared to empty vector (pCMV6) control (**p < 0.01; ***p < 0.001; ****p < 0.0001) or compared to NUMB <t>overexpression</t> (#p < 0.05; ###p < 0.001; ####p < 0.0001 in ≥2 biological replicates with ≥3 technical replicates and 2-3 images per replicate. Scale Bar=400 µm. Statistical significance was determined using one- or two-way ANOVA followed by Fisher’s LSD tests.
Origene Rg209744, supplied by OriGene, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/s17-1/pmc09797337-221-14-14?v=OriGene
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pcmv6 xl5 numb  (OriGene)
90
OriGene pcmv6 xl5 numb
Fig. 5 Cell proliferation, migration, and invasion affected by <t>NUMB</t> modulation in melanoma cells. a Cell proliferation assay was performed using RealTime-Glo MT Cell Viability Assay (Promega) in NUMB-overexpressing (NUMB-wild type; S413A-non-phosphorylatable; S413D-phosphomimetic) melanoma cells till 72 h. b Cell migration was analyzed by wound healing assay in NUMB-modulated melanoma cells at 0, 24 and 48 h post-wound creation. c Cell invasion was analyzed by Matrigel invasion chambers using NUMB-modulated melanoma cells at 24 h. The quantitative data are presented as mean ± SEM with statistical significance compared to empty vector (pCMV6) control (**p < 0.01; ***p < 0.001; ****p < 0.0001) or compared to NUMB <t>overexpression</t> (#p < 0.05; ###p < 0.001; ####p < 0.0001 in ≥2 biological replicates with ≥3 technical replicates and 2-3 images per replicate. Scale Bar=400 µm. Statistical significance was determined using one- or two-way ANOVA followed by Fisher’s LSD tests.
Pcmv6 Xl5 Numb, supplied by OriGene, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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strain e coli s171 λpir  (ATCC)
93
ATCC strain e coli s171 λpir
Fig. 5 Cell proliferation, migration, and invasion affected by <t>NUMB</t> modulation in melanoma cells. a Cell proliferation assay was performed using RealTime-Glo MT Cell Viability Assay (Promega) in NUMB-overexpressing (NUMB-wild type; S413A-non-phosphorylatable; S413D-phosphomimetic) melanoma cells till 72 h. b Cell migration was analyzed by wound healing assay in NUMB-modulated melanoma cells at 0, 24 and 48 h post-wound creation. c Cell invasion was analyzed by Matrigel invasion chambers using NUMB-modulated melanoma cells at 24 h. The quantitative data are presented as mean ± SEM with statistical significance compared to empty vector (pCMV6) control (**p < 0.01; ***p < 0.001; ****p < 0.0001) or compared to NUMB <t>overexpression</t> (#p < 0.05; ###p < 0.001; ####p < 0.0001 in ≥2 biological replicates with ≥3 technical replicates and 2-3 images per replicate. Scale Bar=400 µm. Statistical significance was determined using one- or two-way ANOVA followed by Fisher’s LSD tests.
Strain E Coli S171 λpir, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/s17-1/pm35802499__cb2c00420_si_001-60-2-19?v=ATCC
Average 93 stars, based on 1 article reviews
strain e coli s171 λpir - by Bioz Stars, 2026-06
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e coli s17  (Addgene inc)
90
Addgene inc e coli s17
Fig. 5 Cell proliferation, migration, and invasion affected by <t>NUMB</t> modulation in melanoma cells. a Cell proliferation assay was performed using RealTime-Glo MT Cell Viability Assay (Promega) in NUMB-overexpressing (NUMB-wild type; S413A-non-phosphorylatable; S413D-phosphomimetic) melanoma cells till 72 h. b Cell migration was analyzed by wound healing assay in NUMB-modulated melanoma cells at 0, 24 and 48 h post-wound creation. c Cell invasion was analyzed by Matrigel invasion chambers using NUMB-modulated melanoma cells at 24 h. The quantitative data are presented as mean ± SEM with statistical significance compared to empty vector (pCMV6) control (**p < 0.01; ***p < 0.001; ****p < 0.0001) or compared to NUMB <t>overexpression</t> (#p < 0.05; ###p < 0.001; ####p < 0.0001 in ≥2 biological replicates with ≥3 technical replicates and 2-3 images per replicate. Scale Bar=400 µm. Statistical significance was determined using one- or two-way ANOVA followed by Fisher’s LSD tests.
E Coli S17, supplied by Addgene inc, 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/s17-1/pmc11234330__ab4c00101_si_001-81-35-48?v=Addgene+inc
Average 90 stars, based on 1 article reviews
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s17 1-biotin-scrambled-1  (BIOTAGE)
90
BIOTAGE s17 1-biotin-scrambled-1
Fig. 5 Cell proliferation, migration, and invasion affected by <t>NUMB</t> modulation in melanoma cells. a Cell proliferation assay was performed using RealTime-Glo MT Cell Viability Assay (Promega) in NUMB-overexpressing (NUMB-wild type; S413A-non-phosphorylatable; S413D-phosphomimetic) melanoma cells till 72 h. b Cell migration was analyzed by wound healing assay in NUMB-modulated melanoma cells at 0, 24 and 48 h post-wound creation. c Cell invasion was analyzed by Matrigel invasion chambers using NUMB-modulated melanoma cells at 24 h. The quantitative data are presented as mean ± SEM with statistical significance compared to empty vector (pCMV6) control (**p < 0.01; ***p < 0.001; ****p < 0.0001) or compared to NUMB <t>overexpression</t> (#p < 0.05; ###p < 0.001; ####p < 0.0001 in ≥2 biological replicates with ≥3 technical replicates and 2-3 images per replicate. Scale Bar=400 µm. Statistical significance was determined using one- or two-way ANOVA followed by Fisher’s LSD tests.
S17 1 Biotin Scrambled 1, supplied by BIOTAGE, 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/s17-1/pmc07755081__oc0c01309_si_001-95-375-378?v=BIOTAGE
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e. coli s17-1/ λpir  (BioResource International Inc)
90
BioResource International Inc e. coli s17-1/ λpir
Fig. 5 Cell proliferation, migration, and invasion affected by <t>NUMB</t> modulation in melanoma cells. a Cell proliferation assay was performed using RealTime-Glo MT Cell Viability Assay (Promega) in NUMB-overexpressing (NUMB-wild type; S413A-non-phosphorylatable; S413D-phosphomimetic) melanoma cells till 72 h. b Cell migration was analyzed by wound healing assay in NUMB-modulated melanoma cells at 0, 24 and 48 h post-wound creation. c Cell invasion was analyzed by Matrigel invasion chambers using NUMB-modulated melanoma cells at 24 h. The quantitative data are presented as mean ± SEM with statistical significance compared to empty vector (pCMV6) control (**p < 0.01; ***p < 0.001; ****p < 0.0001) or compared to NUMB <t>overexpression</t> (#p < 0.05; ###p < 0.001; ####p < 0.0001 in ≥2 biological replicates with ≥3 technical replicates and 2-3 images per replicate. Scale Bar=400 µm. Statistical significance was determined using one- or two-way ANOVA followed by Fisher’s LSD tests.
E. Coli S17 1/ λpir, supplied by BioResource International Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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e. coli sm10 λpir kmr  (Biomedal Inc)
90
Biomedal Inc e. coli sm10 λpir kmr
Fig. 5 Cell proliferation, migration, and invasion affected by <t>NUMB</t> modulation in melanoma cells. a Cell proliferation assay was performed using RealTime-Glo MT Cell Viability Assay (Promega) in NUMB-overexpressing (NUMB-wild type; S413A-non-phosphorylatable; S413D-phosphomimetic) melanoma cells till 72 h. b Cell migration was analyzed by wound healing assay in NUMB-modulated melanoma cells at 0, 24 and 48 h post-wound creation. c Cell invasion was analyzed by Matrigel invasion chambers using NUMB-modulated melanoma cells at 24 h. The quantitative data are presented as mean ± SEM with statistical significance compared to empty vector (pCMV6) control (**p < 0.01; ***p < 0.001; ****p < 0.0001) or compared to NUMB <t>overexpression</t> (#p < 0.05; ###p < 0.001; ####p < 0.0001 in ≥2 biological replicates with ≥3 technical replicates and 2-3 images per replicate. Scale Bar=400 µm. Statistical significance was determined using one- or two-way ANOVA followed by Fisher’s LSD tests.
E. Coli Sm10 λpir Kmr, supplied by Biomedal Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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escherichia coli s17-1(λpir  (Beijing TransGen Biotech)
90
Beijing TransGen Biotech escherichia coli s17-1(λpir
Fig. 5 Cell proliferation, migration, and invasion affected by <t>NUMB</t> modulation in melanoma cells. a Cell proliferation assay was performed using RealTime-Glo MT Cell Viability Assay (Promega) in NUMB-overexpressing (NUMB-wild type; S413A-non-phosphorylatable; S413D-phosphomimetic) melanoma cells till 72 h. b Cell migration was analyzed by wound healing assay in NUMB-modulated melanoma cells at 0, 24 and 48 h post-wound creation. c Cell invasion was analyzed by Matrigel invasion chambers using NUMB-modulated melanoma cells at 24 h. The quantitative data are presented as mean ± SEM with statistical significance compared to empty vector (pCMV6) control (**p < 0.01; ***p < 0.001; ****p < 0.0001) or compared to NUMB <t>overexpression</t> (#p < 0.05; ###p < 0.001; ####p < 0.0001 in ≥2 biological replicates with ≥3 technical replicates and 2-3 images per replicate. Scale Bar=400 µm. Statistical significance was determined using one- or two-way ANOVA followed by Fisher’s LSD tests.
Escherichia Coli S17 1(λpir, supplied by Beijing TransGen Biotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Fig. 5 Cell proliferation, migration, and invasion affected by NUMB modulation in melanoma cells. a Cell proliferation assay was performed using RealTime-Glo MT Cell Viability Assay (Promega) in NUMB-overexpressing (NUMB-wild type; S413A-non-phosphorylatable; S413D-phosphomimetic) melanoma cells till 72 h. b Cell migration was analyzed by wound healing assay in NUMB-modulated melanoma cells at 0, 24 and 48 h post-wound creation. c Cell invasion was analyzed by Matrigel invasion chambers using NUMB-modulated melanoma cells at 24 h. The quantitative data are presented as mean ± SEM with statistical significance compared to empty vector (pCMV6) control (**p < 0.01; ***p < 0.001; ****p < 0.0001) or compared to NUMB overexpression (#p < 0.05; ###p < 0.001; ####p < 0.0001 in ≥2 biological replicates with ≥3 technical replicates and 2-3 images per replicate. Scale Bar=400 µm. Statistical significance was determined using one- or two-way ANOVA followed by Fisher’s LSD tests.

Journal: NPJ precision oncology

Article Title: Role of PLK1/NUMB/NOTCH in epithelial-mesenchymal transition in human melanoma.

doi: 10.1038/s41698-023-00493-7

Figure Lengend Snippet: Fig. 5 Cell proliferation, migration, and invasion affected by NUMB modulation in melanoma cells. a Cell proliferation assay was performed using RealTime-Glo MT Cell Viability Assay (Promega) in NUMB-overexpressing (NUMB-wild type; S413A-non-phosphorylatable; S413D-phosphomimetic) melanoma cells till 72 h. b Cell migration was analyzed by wound healing assay in NUMB-modulated melanoma cells at 0, 24 and 48 h post-wound creation. c Cell invasion was analyzed by Matrigel invasion chambers using NUMB-modulated melanoma cells at 24 h. The quantitative data are presented as mean ± SEM with statistical significance compared to empty vector (pCMV6) control (**p < 0.01; ***p < 0.001; ****p < 0.0001) or compared to NUMB overexpression (#p < 0.05; ###p < 0.001; ####p < 0.0001 in ≥2 biological replicates with ≥3 technical replicates and 2-3 images per replicate. Scale Bar=400 µm. Statistical significance was determined using one- or two-way ANOVA followed by Fisher’s LSD tests.

Article Snippet: Empty vector (pCMV6-Entry #PS100001) and NUMB overexpression plasmids were purchased from Origene (WT NUMB #RC220960 with custom mutated plasmids containing S413A and S413D mutations).

Techniques: Migration, Proliferation Assay, Viability Assay, Wound Healing Assay, Plasmid Preparation, Control, Over Expression