replication strain atcc 12202 Search Results


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ATCC enterococcus faecium atcc 12202 vancomycin resistant
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Mutation at leucine 7 of N17 domain suppresses HTT-Q73 association with mitochondria . A , schematic representation of detecting mitochondrial localization of HTT-Q73 mutants. B and C , Western blotting and quantitative analysis of Myc-tagged wildtype (WT) HTT-Q73 and N17 domain-truncated HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. ATPB: loading control of mitochondrial fractions; Actin: loading control of whole cell lysates (WCLs). One-way ANOVA was conducted, followed by Dunnett's multiple comparisons test (related to HTT-Q73-WT). D , Western blotting of the expression of HTT-Q73 mutants (WT, L7A, M8A, and F11A) and HTT-Q23 in WCL of N2a cells at 72 h post-transfection. E and F , Western blotting and quantitative analysis of the expression of HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. <t>Matrin3:</t> loading control of nuclear fractions; ENO3: loading control of cytosol fractions. One-way ANOVA was conducted, followed by Tukey's multiple comparison test. G and H , Western blotting and quantitative analysis of the expression level of Q73-L7A mutant in nuclear fractions and WCL of N2a cells at 72 h post-transfection. Unpaired t test was conducted. n = 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001. HTT-Q73, HTT exon 1 with 73 glutamine repeats.
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Mutation at leucine 7 of N17 domain suppresses HTT-Q73 association with mitochondria . A , schematic representation of detecting mitochondrial localization of HTT-Q73 mutants. B and C , Western blotting and quantitative analysis of Myc-tagged wildtype (WT) HTT-Q73 and N17 domain-truncated HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. ATPB: loading control of mitochondrial fractions; Actin: loading control of whole cell lysates (WCLs). One-way ANOVA was conducted, followed by Dunnett's multiple comparisons test (related to HTT-Q73-WT). D , Western blotting of the expression of HTT-Q73 mutants (WT, L7A, M8A, and F11A) and HTT-Q23 in WCL of N2a cells at 72 h post-transfection. E and F , Western blotting and quantitative analysis of the expression of HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. <t>Matrin3:</t> loading control of nuclear fractions; ENO3: loading control of cytosol fractions. One-way ANOVA was conducted, followed by Tukey's multiple comparison test. G and H , Western blotting and quantitative analysis of the expression level of Q73-L7A mutant in nuclear fractions and WCL of N2a cells at 72 h post-transfection. Unpaired t test was conducted. n = 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001. HTT-Q73, HTT exon 1 with 73 glutamine repeats.
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PromoCell human umbilical artery endothelial cells
Mutation at leucine 7 of N17 domain suppresses HTT-Q73 association with mitochondria . A , schematic representation of detecting mitochondrial localization of HTT-Q73 mutants. B and C , Western blotting and quantitative analysis of Myc-tagged wildtype (WT) HTT-Q73 and N17 domain-truncated HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. ATPB: loading control of mitochondrial fractions; Actin: loading control of whole cell lysates (WCLs). One-way ANOVA was conducted, followed by Dunnett's multiple comparisons test (related to HTT-Q73-WT). D , Western blotting of the expression of HTT-Q73 mutants (WT, L7A, M8A, and F11A) and HTT-Q23 in WCL of N2a cells at 72 h post-transfection. E and F , Western blotting and quantitative analysis of the expression of HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. <t>Matrin3:</t> loading control of nuclear fractions; ENO3: loading control of cytosol fractions. One-way ANOVA was conducted, followed by Tukey's multiple comparison test. G and H , Western blotting and quantitative analysis of the expression level of Q73-L7A mutant in nuclear fractions and WCL of N2a cells at 72 h post-transfection. Unpaired t test was conducted. n = 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001. HTT-Q73, HTT exon 1 with 73 glutamine repeats.
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Cell Signaling Technology Inc ki67
Mutation at leucine 7 of N17 domain suppresses HTT-Q73 association with mitochondria . A , schematic representation of detecting mitochondrial localization of HTT-Q73 mutants. B and C , Western blotting and quantitative analysis of Myc-tagged wildtype (WT) HTT-Q73 and N17 domain-truncated HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. ATPB: loading control of mitochondrial fractions; Actin: loading control of whole cell lysates (WCLs). One-way ANOVA was conducted, followed by Dunnett's multiple comparisons test (related to HTT-Q73-WT). D , Western blotting of the expression of HTT-Q73 mutants (WT, L7A, M8A, and F11A) and HTT-Q23 in WCL of N2a cells at 72 h post-transfection. E and F , Western blotting and quantitative analysis of the expression of HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. <t>Matrin3:</t> loading control of nuclear fractions; ENO3: loading control of cytosol fractions. One-way ANOVA was conducted, followed by Tukey's multiple comparison test. G and H , Western blotting and quantitative analysis of the expression level of Q73-L7A mutant in nuclear fractions and WCL of N2a cells at 72 h post-transfection. Unpaired t test was conducted. n = 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001. HTT-Q73, HTT exon 1 with 73 glutamine repeats.
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Promega oligofectamine transfection reagent
Mutation at leucine 7 of N17 domain suppresses HTT-Q73 association with mitochondria . A , schematic representation of detecting mitochondrial localization of HTT-Q73 mutants. B and C , Western blotting and quantitative analysis of Myc-tagged wildtype (WT) HTT-Q73 and N17 domain-truncated HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. ATPB: loading control of mitochondrial fractions; Actin: loading control of whole cell lysates (WCLs). One-way ANOVA was conducted, followed by Dunnett's multiple comparisons test (related to HTT-Q73-WT). D , Western blotting of the expression of HTT-Q73 mutants (WT, L7A, M8A, and F11A) and HTT-Q23 in WCL of N2a cells at 72 h post-transfection. E and F , Western blotting and quantitative analysis of the expression of HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. <t>Matrin3:</t> loading control of nuclear fractions; ENO3: loading control of cytosol fractions. One-way ANOVA was conducted, followed by Tukey's multiple comparison test. G and H , Western blotting and quantitative analysis of the expression level of Q73-L7A mutant in nuclear fractions and WCL of N2a cells at 72 h post-transfection. Unpaired t test was conducted. n = 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001. HTT-Q73, HTT exon 1 with 73 glutamine repeats.
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ABclonal Biotechnology h3k4me3 a22146 antibody
Mutation at leucine 7 of N17 domain suppresses HTT-Q73 association with mitochondria . A , schematic representation of detecting mitochondrial localization of HTT-Q73 mutants. B and C , Western blotting and quantitative analysis of Myc-tagged wildtype (WT) HTT-Q73 and N17 domain-truncated HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. ATPB: loading control of mitochondrial fractions; Actin: loading control of whole cell lysates (WCLs). One-way ANOVA was conducted, followed by Dunnett's multiple comparisons test (related to HTT-Q73-WT). D , Western blotting of the expression of HTT-Q73 mutants (WT, L7A, M8A, and F11A) and HTT-Q23 in WCL of N2a cells at 72 h post-transfection. E and F , Western blotting and quantitative analysis of the expression of HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. <t>Matrin3:</t> loading control of nuclear fractions; ENO3: loading control of cytosol fractions. One-way ANOVA was conducted, followed by Tukey's multiple comparison test. G and H , Western blotting and quantitative analysis of the expression level of Q73-L7A mutant in nuclear fractions and WCL of N2a cells at 72 h post-transfection. Unpaired t test was conducted. n = 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001. HTT-Q73, HTT exon 1 with 73 glutamine repeats.
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Cell Signaling Technology Inc 62548 cd31
Mutation at leucine 7 of N17 domain suppresses HTT-Q73 association with mitochondria . A , schematic representation of detecting mitochondrial localization of HTT-Q73 mutants. B and C , Western blotting and quantitative analysis of Myc-tagged wildtype (WT) HTT-Q73 and N17 domain-truncated HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. ATPB: loading control of mitochondrial fractions; Actin: loading control of whole cell lysates (WCLs). One-way ANOVA was conducted, followed by Dunnett's multiple comparisons test (related to HTT-Q73-WT). D , Western blotting of the expression of HTT-Q73 mutants (WT, L7A, M8A, and F11A) and HTT-Q23 in WCL of N2a cells at 72 h post-transfection. E and F , Western blotting and quantitative analysis of the expression of HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. <t>Matrin3:</t> loading control of nuclear fractions; ENO3: loading control of cytosol fractions. One-way ANOVA was conducted, followed by Tukey's multiple comparison test. G and H , Western blotting and quantitative analysis of the expression level of Q73-L7A mutant in nuclear fractions and WCL of N2a cells at 72 h post-transfection. Unpaired t test was conducted. n = 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001. HTT-Q73, HTT exon 1 with 73 glutamine repeats.
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Image Search Results


Mutation at leucine 7 of N17 domain suppresses HTT-Q73 association with mitochondria . A , schematic representation of detecting mitochondrial localization of HTT-Q73 mutants. B and C , Western blotting and quantitative analysis of Myc-tagged wildtype (WT) HTT-Q73 and N17 domain-truncated HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. ATPB: loading control of mitochondrial fractions; Actin: loading control of whole cell lysates (WCLs). One-way ANOVA was conducted, followed by Dunnett's multiple comparisons test (related to HTT-Q73-WT). D , Western blotting of the expression of HTT-Q73 mutants (WT, L7A, M8A, and F11A) and HTT-Q23 in WCL of N2a cells at 72 h post-transfection. E and F , Western blotting and quantitative analysis of the expression of HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. Matrin3: loading control of nuclear fractions; ENO3: loading control of cytosol fractions. One-way ANOVA was conducted, followed by Tukey's multiple comparison test. G and H , Western blotting and quantitative analysis of the expression level of Q73-L7A mutant in nuclear fractions and WCL of N2a cells at 72 h post-transfection. Unpaired t test was conducted. n = 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001. HTT-Q73, HTT exon 1 with 73 glutamine repeats.

Journal: The Journal of Biological Chemistry

Article Title: Leucine 7 is a key residue for mutant huntingtin–induced mitochondrial pathology and neurotoxicity in Huntington's disease

doi: 10.1016/j.jbc.2025.108297

Figure Lengend Snippet: Mutation at leucine 7 of N17 domain suppresses HTT-Q73 association with mitochondria . A , schematic representation of detecting mitochondrial localization of HTT-Q73 mutants. B and C , Western blotting and quantitative analysis of Myc-tagged wildtype (WT) HTT-Q73 and N17 domain-truncated HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. ATPB: loading control of mitochondrial fractions; Actin: loading control of whole cell lysates (WCLs). One-way ANOVA was conducted, followed by Dunnett's multiple comparisons test (related to HTT-Q73-WT). D , Western blotting of the expression of HTT-Q73 mutants (WT, L7A, M8A, and F11A) and HTT-Q23 in WCL of N2a cells at 72 h post-transfection. E and F , Western blotting and quantitative analysis of the expression of HTT-Q73 mutants in mitochondrial fractions of N2a cells at 72 h post-transfection. n = 3 independent experiments. Matrin3: loading control of nuclear fractions; ENO3: loading control of cytosol fractions. One-way ANOVA was conducted, followed by Tukey's multiple comparison test. G and H , Western blotting and quantitative analysis of the expression level of Q73-L7A mutant in nuclear fractions and WCL of N2a cells at 72 h post-transfection. Unpaired t test was conducted. n = 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001. HTT-Q73, HTT exon 1 with 73 glutamine repeats.

Article Snippet: Primary antibodies were diluted 1:1000 and applied as follows: c-Myc (SC-40, Santa Cruz), actin (TA-09, ZSGB-BIO), DRP1 (611,113, BD Biosciences), MFN1 (13798-1-AP, Proteintech), MFN2 (12186-1-AP, Proteintech), ENO3 (15421-1-AP, Proteintech), Matrin3 (12202-2-AP, Proteintech), TFAM (ab131607, Abcam), OPA1 (27733-1-AP, Proteintech), mtCO2 (55070-1-AP, Proteintech), PGC1-α (NBP104676, Novus), cleaved PARP (9541S, CST), ATPB (17247-1-AP, Proteintech), RNaseH1 (15606-1-AP, Proteintech), Poly-γ (A8451, Abclonal), VDAC (55259-1-AP, Proteintech), Cytochrome-C (10993-1-AP, Proteintech), and MnSOD (611580, BD Biosciences).

Techniques: Mutagenesis, Western Blot, Transfection, Control, Expressing, Comparison