mycn Search Results


91
Sino Biological mouse nqo1 complementary dna cdna
Mouse Nqo1 Complementary Dna Cdna, supplied by Sino Biological, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Santa Cruz Biotechnology n myc
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Cell Signaling Technology Inc mycn antibody
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Cell Signaling Technology Inc anti n myc
Anti N Myc, supplied by Cell Signaling Technology Inc, 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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Cell Signaling Technology Inc c myc
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Proteintech mycn
Fig. 2 <t>|</t> <t>Runx1t1</t> loss reverses <t>MYCN-mediated</t> sustained hyperplasia and induces ganglia neurite extension. a The percentage neuroblast hyperplasia scored from homozygous Th-MYCN (+/+) mice or littermate mice lacking the MYCN transgene (−/−), with either wild-type (+/+) or heterozygous loss (+/−) of Runx1t1. Scoring of N = 3–8 independent mice was performed for each genotype and timepoint. All data points were N = 3, except for +/+, +/+ week 1 and week 2 (N = 4); +/+, +/−day 0 (N = 8) and week 4 (N = 4); −/−, +/−day 0 (N = 6), week 1 (N = 4) and week 4 (N = 5). The graph is mean ± SEM. b Representative histology of RUNX1T1 staining in ganglia from mice homozygous for the Th-MYCN transgene, and either wild-type or heterozygous for Runx1t1 from day 0 and 4 weeks of age.
Mycn, 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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Cell Signaling Technology Inc anti n myc rabbit polyclonal antibodies
Fig. 2 <t>|</t> <t>Runx1t1</t> loss reverses <t>MYCN-mediated</t> sustained hyperplasia and induces ganglia neurite extension. a The percentage neuroblast hyperplasia scored from homozygous Th-MYCN (+/+) mice or littermate mice lacking the MYCN transgene (−/−), with either wild-type (+/+) or heterozygous loss (+/−) of Runx1t1. Scoring of N = 3–8 independent mice was performed for each genotype and timepoint. All data points were N = 3, except for +/+, +/+ week 1 and week 2 (N = 4); +/+, +/−day 0 (N = 8) and week 4 (N = 4); −/−, +/−day 0 (N = 6), week 1 (N = 4) and week 4 (N = 5). The graph is mean ± SEM. b Representative histology of RUNX1T1 staining in ganglia from mice homozygous for the Th-MYCN transgene, and either wild-type or heterozygous for Runx1t1 from day 0 and 4 weeks of age.
Anti N Myc Rabbit Polyclonal Antibodies, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
Addgene inc otoferlin amino acids 1
Multiple C2 domains mediate otoferlin–Loop1.3 interaction. (A–D) Binding curves for immobilized YFP-otoferlin C2A (A), C2B (B), C2D (C), and C2F (D) domains titrated against Loop1.3 at 0.1–50 µM free calcium. Data are fit with a Langmuir isotherm (solid lines). Insets depict 0–10 µM for clarity. Each experimental data point represents the mean value of n = 3. (E and F) Binding curves for immobilized YFP-otoferlin C2C and C2E domains titrated against Loop1.3. Colocalization between Loop1.3 and YFP-otoferlin (otoferlin amino acids 1–1,885) is included for comparison.
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Proteintech resource source identifier antibodies targ1
Multiple C2 domains mediate otoferlin–Loop1.3 interaction. (A–D) Binding curves for immobilized YFP-otoferlin C2A (A), C2B (B), C2D (C), and C2F (D) domains titrated against Loop1.3 at 0.1–50 µM free calcium. Data are fit with a Langmuir isotherm (solid lines). Insets depict 0–10 µM for clarity. Each experimental data point represents the mean value of n = 3. (E and F) Binding curves for immobilized YFP-otoferlin C2C and C2E domains titrated against Loop1.3. Colocalization between Loop1.3 and YFP-otoferlin (otoferlin amino acids 1–1,885) is included for comparison.
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92
Sino Biological n terminal myc tag
Multiple C2 domains mediate otoferlin–Loop1.3 interaction. (A–D) Binding curves for immobilized YFP-otoferlin C2A (A), C2B (B), C2D (C), and C2F (D) domains titrated against Loop1.3 at 0.1–50 µM free calcium. Data are fit with a Langmuir isotherm (solid lines). Insets depict 0–10 µM for clarity. Each experimental data point represents the mean value of n = 3. (E and F) Binding curves for immobilized YFP-otoferlin C2C and C2E domains titrated against Loop1.3. Colocalization between Loop1.3 and YFP-otoferlin (otoferlin amino acids 1–1,885) is included for comparison.
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Sino Biological n myc parp1
Multiple C2 domains mediate otoferlin–Loop1.3 interaction. (A–D) Binding curves for immobilized YFP-otoferlin C2A (A), C2B (B), C2D (C), and C2F (D) domains titrated against Loop1.3 at 0.1–50 µM free calcium. Data are fit with a Langmuir isotherm (solid lines). Insets depict 0–10 µM for clarity. Each experimental data point represents the mean value of n = 3. (E and F) Binding curves for immobilized YFP-otoferlin C2C and C2E domains titrated against Loop1.3. Colocalization between Loop1.3 and YFP-otoferlin (otoferlin amino acids 1–1,885) is included for comparison.
N Myc Parp1, supplied by Sino Biological, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Fig. 2 | Runx1t1 loss reverses MYCN-mediated sustained hyperplasia and induces ganglia neurite extension. a The percentage neuroblast hyperplasia scored from homozygous Th-MYCN (+/+) mice or littermate mice lacking the MYCN transgene (−/−), with either wild-type (+/+) or heterozygous loss (+/−) of Runx1t1. Scoring of N = 3–8 independent mice was performed for each genotype and timepoint. All data points were N = 3, except for +/+, +/+ week 1 and week 2 (N = 4); +/+, +/−day 0 (N = 8) and week 4 (N = 4); −/−, +/−day 0 (N = 6), week 1 (N = 4) and week 4 (N = 5). The graph is mean ± SEM. b Representative histology of RUNX1T1 staining in ganglia from mice homozygous for the Th-MYCN transgene, and either wild-type or heterozygous for Runx1t1 from day 0 and 4 weeks of age.

Journal: Nature communications

Article Title: The transcriptional co-repressor Runx1t1 is essential for MYCN-driven neuroblastoma tumorigenesis.

doi: 10.1038/s41467-024-49871-0

Figure Lengend Snippet: Fig. 2 | Runx1t1 loss reverses MYCN-mediated sustained hyperplasia and induces ganglia neurite extension. a The percentage neuroblast hyperplasia scored from homozygous Th-MYCN (+/+) mice or littermate mice lacking the MYCN transgene (−/−), with either wild-type (+/+) or heterozygous loss (+/−) of Runx1t1. Scoring of N = 3–8 independent mice was performed for each genotype and timepoint. All data points were N = 3, except for +/+, +/+ week 1 and week 2 (N = 4); +/+, +/−day 0 (N = 8) and week 4 (N = 4); −/−, +/−day 0 (N = 6), week 1 (N = 4) and week 4 (N = 5). The graph is mean ± SEM. b Representative histology of RUNX1T1 staining in ganglia from mice homozygous for the Th-MYCN transgene, and either wild-type or heterozygous for Runx1t1 from day 0 and 4 weeks of age.

Article Snippet: Samples were embedded in paraffin, sectioned, and stained with H&E or for MYCN (rabbit polyclonal antibody, 10159-2-AP, Proteintech, 1:1000) and RUNX1T1 (as described above).

Techniques: Staining

Multiple C2 domains mediate otoferlin–Loop1.3 interaction. (A–D) Binding curves for immobilized YFP-otoferlin C2A (A), C2B (B), C2D (C), and C2F (D) domains titrated against Loop1.3 at 0.1–50 µM free calcium. Data are fit with a Langmuir isotherm (solid lines). Insets depict 0–10 µM for clarity. Each experimental data point represents the mean value of n = 3. (E and F) Binding curves for immobilized YFP-otoferlin C2C and C2E domains titrated against Loop1.3. Colocalization between Loop1.3 and YFP-otoferlin (otoferlin amino acids 1–1,885) is included for comparison.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Article Title: Otoferlin is a multivalent calcium-sensitive scaffold linking SNAREs and calcium channels

doi: 10.1073/pnas.1703240114

Figure Lengend Snippet: Multiple C2 domains mediate otoferlin–Loop1.3 interaction. (A–D) Binding curves for immobilized YFP-otoferlin C2A (A), C2B (B), C2D (C), and C2F (D) domains titrated against Loop1.3 at 0.1–50 µM free calcium. Data are fit with a Langmuir isotherm (solid lines). Insets depict 0–10 µM for clarity. Each experimental data point represents the mean value of n = 3. (E and F) Binding curves for immobilized YFP-otoferlin C2C and C2E domains titrated against Loop1.3. Colocalization between Loop1.3 and YFP-otoferlin (otoferlin amino acids 1–1,885) is included for comparison.

Article Snippet: Otoferlin amino acids 1–1,885 were amplified via PCR from a PCDNA3 vector and subcloned into the HindIII and BamHI sites of the CKAR vector acquired from Addgene (plasmid 14860).

Techniques: Binding Assay