mouse anti breast cancer gene 1 Search Results


93
Santa Cruz Biotechnology mouse anti tieg1 klf10 monoclonal antibody
Fig. 4. <t>Klf10</t> was upregulated in the ventricles of STZ mice, A qRT-PCR analysis of Klf4 in the ventricle of control, STZ-4W or insulin-treated STZ-4W STZ-4W þ Ins) mice. Each data represents the mean ± SEM (n ¼ 6e9). ****p < 0.0001 by ANOVA post hoc Tukey's test. B. The correlation between the expression levels of Klf4 and Klf10 (r ¼ 0.3989, p ¼ 0.0733). C qRT-PCR analysis of Klf10. Each data represents the mean ± SEM (n ¼ 6e9). *p < 0.05 by ANOVA post hoc Tukey's test. D. The correlation between the expression levels of Nrg1 and Klf10 (r ¼ 0.7935, p ¼ 0.0001). E. Perinuclear localization of Klf 10 (green), CD31 (magenta) and DAPI (cyan) in the ventricles of control and STZ-4W mice. For RT-PCR, relative quantification (RQ) of the gene expression was calculated with the comparative Ct method. Hprt was used as an internal reference.
Mouse Anti Tieg1 Klf10 Monoclonal Antibody, supplied by Santa Cruz Biotechnology, 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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StressMarq enac subunits
Fig. 4. <t>Klf10</t> was upregulated in the ventricles of STZ mice, A qRT-PCR analysis of Klf4 in the ventricle of control, STZ-4W or insulin-treated STZ-4W STZ-4W þ Ins) mice. Each data represents the mean ± SEM (n ¼ 6e9). ****p < 0.0001 by ANOVA post hoc Tukey's test. B. The correlation between the expression levels of Klf4 and Klf10 (r ¼ 0.3989, p ¼ 0.0733). C qRT-PCR analysis of Klf10. Each data represents the mean ± SEM (n ¼ 6e9). *p < 0.05 by ANOVA post hoc Tukey's test. D. The correlation between the expression levels of Nrg1 and Klf10 (r ¼ 0.7935, p ¼ 0.0001). E. Perinuclear localization of Klf 10 (green), CD31 (magenta) and DAPI (cyan) in the ventricles of control and STZ-4W mice. For RT-PCR, relative quantification (RQ) of the gene expression was calculated with the comparative Ct method. Hprt was used as an internal reference.
Enac Subunits, supplied by StressMarq, 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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Santa Cruz Biotechnology mouse anti net1
Fig. 4. <t>Klf10</t> was upregulated in the ventricles of STZ mice, A qRT-PCR analysis of Klf4 in the ventricle of control, STZ-4W or insulin-treated STZ-4W STZ-4W þ Ins) mice. Each data represents the mean ± SEM (n ¼ 6e9). ****p < 0.0001 by ANOVA post hoc Tukey's test. B. The correlation between the expression levels of Klf4 and Klf10 (r ¼ 0.3989, p ¼ 0.0733). C qRT-PCR analysis of Klf10. Each data represents the mean ± SEM (n ¼ 6e9). *p < 0.05 by ANOVA post hoc Tukey's test. D. The correlation between the expression levels of Nrg1 and Klf10 (r ¼ 0.7935, p ¼ 0.0001). E. Perinuclear localization of Klf 10 (green), CD31 (magenta) and DAPI (cyan) in the ventricles of control and STZ-4W mice. For RT-PCR, relative quantification (RQ) of the gene expression was calculated with the comparative Ct method. Hprt was used as an internal reference.
Mouse Anti Net1, supplied by Santa Cruz Biotechnology, 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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Cell Signaling Technology Inc anti immune responsive gene 1 irg1
Fig. 4. <t>Klf10</t> was upregulated in the ventricles of STZ mice, A qRT-PCR analysis of Klf4 in the ventricle of control, STZ-4W or insulin-treated STZ-4W STZ-4W þ Ins) mice. Each data represents the mean ± SEM (n ¼ 6e9). ****p < 0.0001 by ANOVA post hoc Tukey's test. B. The correlation between the expression levels of Klf4 and Klf10 (r ¼ 0.3989, p ¼ 0.0733). C qRT-PCR analysis of Klf10. Each data represents the mean ± SEM (n ¼ 6e9). *p < 0.05 by ANOVA post hoc Tukey's test. D. The correlation between the expression levels of Nrg1 and Klf10 (r ¼ 0.7935, p ¼ 0.0001). E. Perinuclear localization of Klf 10 (green), CD31 (magenta) and DAPI (cyan) in the ventricles of control and STZ-4W mice. For RT-PCR, relative quantification (RQ) of the gene expression was calculated with the comparative Ct method. Hprt was used as an internal reference.
Anti Immune Responsive Gene 1 Irg1, 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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Proteintech anti myotubularin related protein 12
Fig. 4. <t>Klf10</t> was upregulated in the ventricles of STZ mice, A qRT-PCR analysis of Klf4 in the ventricle of control, STZ-4W or insulin-treated STZ-4W STZ-4W þ Ins) mice. Each data represents the mean ± SEM (n ¼ 6e9). ****p < 0.0001 by ANOVA post hoc Tukey's test. B. The correlation between the expression levels of Klf4 and Klf10 (r ¼ 0.3989, p ¼ 0.0733). C qRT-PCR analysis of Klf10. Each data represents the mean ± SEM (n ¼ 6e9). *p < 0.05 by ANOVA post hoc Tukey's test. D. The correlation between the expression levels of Nrg1 and Klf10 (r ¼ 0.7935, p ¼ 0.0001). E. Perinuclear localization of Klf 10 (green), CD31 (magenta) and DAPI (cyan) in the ventricles of control and STZ-4W mice. For RT-PCR, relative quantification (RQ) of the gene expression was calculated with the comparative Ct method. Hprt was used as an internal reference.
Anti Myotubularin Related Protein 12, 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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Boster Bio tumor susceptibility gene 101
Fig. 4. <t>Klf10</t> was upregulated in the ventricles of STZ mice, A qRT-PCR analysis of Klf4 in the ventricle of control, STZ-4W or insulin-treated STZ-4W STZ-4W þ Ins) mice. Each data represents the mean ± SEM (n ¼ 6e9). ****p < 0.0001 by ANOVA post hoc Tukey's test. B. The correlation between the expression levels of Klf4 and Klf10 (r ¼ 0.3989, p ¼ 0.0733). C qRT-PCR analysis of Klf10. Each data represents the mean ± SEM (n ¼ 6e9). *p < 0.05 by ANOVA post hoc Tukey's test. D. The correlation between the expression levels of Nrg1 and Klf10 (r ¼ 0.7935, p ¼ 0.0001). E. Perinuclear localization of Klf 10 (green), CD31 (magenta) and DAPI (cyan) in the ventricles of control and STZ-4W mice. For RT-PCR, relative quantification (RQ) of the gene expression was calculated with the comparative Ct method. Hprt was used as an internal reference.
Tumor Susceptibility Gene 101, supplied by Boster Bio, 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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GeneTex gtx632015 antibody
Fig. 4. <t>Klf10</t> was upregulated in the ventricles of STZ mice, A qRT-PCR analysis of Klf4 in the ventricle of control, STZ-4W or insulin-treated STZ-4W STZ-4W þ Ins) mice. Each data represents the mean ± SEM (n ¼ 6e9). ****p < 0.0001 by ANOVA post hoc Tukey's test. B. The correlation between the expression levels of Klf4 and Klf10 (r ¼ 0.3989, p ¼ 0.0733). C qRT-PCR analysis of Klf10. Each data represents the mean ± SEM (n ¼ 6e9). *p < 0.05 by ANOVA post hoc Tukey's test. D. The correlation between the expression levels of Nrg1 and Klf10 (r ¼ 0.7935, p ¼ 0.0001). E. Perinuclear localization of Klf 10 (green), CD31 (magenta) and DAPI (cyan) in the ventricles of control and STZ-4W mice. For RT-PCR, relative quantification (RQ) of the gene expression was calculated with the comparative Ct method. Hprt was used as an internal reference.
Gtx632015 Antibody, supplied by GeneTex, 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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Novus Biologicals rabbit polyclonal anti brca1
Fig. 4. <t>Klf10</t> was upregulated in the ventricles of STZ mice, A qRT-PCR analysis of Klf4 in the ventricle of control, STZ-4W or insulin-treated STZ-4W STZ-4W þ Ins) mice. Each data represents the mean ± SEM (n ¼ 6e9). ****p < 0.0001 by ANOVA post hoc Tukey's test. B. The correlation between the expression levels of Klf4 and Klf10 (r ¼ 0.3989, p ¼ 0.0733). C qRT-PCR analysis of Klf10. Each data represents the mean ± SEM (n ¼ 6e9). *p < 0.05 by ANOVA post hoc Tukey's test. D. The correlation between the expression levels of Nrg1 and Klf10 (r ¼ 0.7935, p ¼ 0.0001). E. Perinuclear localization of Klf 10 (green), CD31 (magenta) and DAPI (cyan) in the ventricles of control and STZ-4W mice. For RT-PCR, relative quantification (RQ) of the gene expression was calculated with the comparative Ct method. Hprt was used as an internal reference.
Rabbit Polyclonal Anti Brca1, supplied by Novus Biologicals, 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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Boster Bio rabbit polyclonal antibody for glut4
Primers for real-time PCR.
Rabbit Polyclonal Antibody For Glut4, supplied by Boster Bio, 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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Proteintech rabbit anti hspb8
Primers for real-time PCR.
Rabbit Anti Hspb8, supplied by Proteintech, 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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Proteintech rabbit anti nbr1
Primers for real-time PCR.
Rabbit Anti Nbr1, supplied by Proteintech, 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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Thermo Fisher gene exp cxcl10 mm00445235 m1
Primers for real-time PCR.
Gene Exp Cxcl10 Mm00445235 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Fig. 4. Klf10 was upregulated in the ventricles of STZ mice, A qRT-PCR analysis of Klf4 in the ventricle of control, STZ-4W or insulin-treated STZ-4W STZ-4W þ Ins) mice. Each data represents the mean ± SEM (n ¼ 6e9). ****p < 0.0001 by ANOVA post hoc Tukey's test. B. The correlation between the expression levels of Klf4 and Klf10 (r ¼ 0.3989, p ¼ 0.0733). C qRT-PCR analysis of Klf10. Each data represents the mean ± SEM (n ¼ 6e9). *p < 0.05 by ANOVA post hoc Tukey's test. D. The correlation between the expression levels of Nrg1 and Klf10 (r ¼ 0.7935, p ¼ 0.0001). E. Perinuclear localization of Klf 10 (green), CD31 (magenta) and DAPI (cyan) in the ventricles of control and STZ-4W mice. For RT-PCR, relative quantification (RQ) of the gene expression was calculated with the comparative Ct method. Hprt was used as an internal reference.

Journal: Journal of pharmacological sciences

Article Title: Compensatory role of neuregulin-1 in diabetic cardiomyopathy.

doi: 10.1016/j.jphs.2023.08.009

Figure Lengend Snippet: Fig. 4. Klf10 was upregulated in the ventricles of STZ mice, A qRT-PCR analysis of Klf4 in the ventricle of control, STZ-4W or insulin-treated STZ-4W STZ-4W þ Ins) mice. Each data represents the mean ± SEM (n ¼ 6e9). ****p < 0.0001 by ANOVA post hoc Tukey's test. B. The correlation between the expression levels of Klf4 and Klf10 (r ¼ 0.3989, p ¼ 0.0733). C qRT-PCR analysis of Klf10. Each data represents the mean ± SEM (n ¼ 6e9). *p < 0.05 by ANOVA post hoc Tukey's test. D. The correlation between the expression levels of Nrg1 and Klf10 (r ¼ 0.7935, p ¼ 0.0001). E. Perinuclear localization of Klf 10 (green), CD31 (magenta) and DAPI (cyan) in the ventricles of control and STZ-4W mice. For RT-PCR, relative quantification (RQ) of the gene expression was calculated with the comparative Ct method. Hprt was used as an internal reference.

Article Snippet: Cryostat sections (15 mm) were incubated overnight at 4 C with the following primary antibodies: mouse antieneuregulin-1 monoclonal antibody (1:100; Santa Cruz Biotechnology, Dallas, TX, USA), rat anti-CD31 monoclonal antibody (1:50; BD Pharmingen, Franklin Lakes, NJ, USA), or mouse anti-TIEG1 (KLF10) monoclonal antibody (1:50; Santa Cruz Biotechnology).

Techniques: Quantitative RT-PCR, Control, Expressing, Reverse Transcription Polymerase Chain Reaction, Gene Expression

Primers for real-time PCR.

Journal: Evidence-based Complementary and Alternative Medicine : eCAM

Article Title: Acupuncture Alters Expression of Insulin Signaling Related Molecules and Improves Insulin Resistance in OLETF Rats

doi: 10.1155/2016/9651592

Figure Lengend Snippet: Primers for real-time PCR.

Article Snippet: Nonspecific binding sites were blocked with 5% milk powder diluted in TBS with 0.05% Tween 20 (TBST) for 60 min. Proteins were detected using the following antibodies: rabbit polyclonal antibody for PI3K-p85 (diluted 1 : 3000; Bios; bs-0128R), rabbit polyclonal antibody for phospho-PKC ζ / λ (diluted 1 : 3000; CST; #9378), rabbit polyclonal antibody for GLUT4 (diluted 1 : 3000; Boster; BA1626), and mouse monoclonal antibody for GAPDH (diluted 1 : 3000; Boster; BM1623).

Techniques:

Effects of acupuncture on mRNA expressions of IRS1, IRS2, PI3K-p85 α , Akt2, aPKC ζ , aPKC λ , and GLUT4 in skeletal muscle of OLETF rats. Acupuncture was applied to the indicated region for 20 min per day, over the course of 21 days. Following administration, the musculus quadriceps femoris was obtained. Relative mRNA expression was determined by real-time RT-PCR. Data are showed as mean ± standard deviation (SD) ( n = 8 each group). ∗∗ P < 0.01 versus SD group; △ P < 0.05 and △△ P < 0.01 versus OLETF group. IRS1: insulin receptor substrate 1; IRS2: insulin receptor substrate 2; PI3K: phosphatidylinositol-3 kinase; PKC: protein kinase C; GLUT4: glucose transporter 4; Akt2: protein kinase B beta.

Journal: Evidence-based Complementary and Alternative Medicine : eCAM

Article Title: Acupuncture Alters Expression of Insulin Signaling Related Molecules and Improves Insulin Resistance in OLETF Rats

doi: 10.1155/2016/9651592

Figure Lengend Snippet: Effects of acupuncture on mRNA expressions of IRS1, IRS2, PI3K-p85 α , Akt2, aPKC ζ , aPKC λ , and GLUT4 in skeletal muscle of OLETF rats. Acupuncture was applied to the indicated region for 20 min per day, over the course of 21 days. Following administration, the musculus quadriceps femoris was obtained. Relative mRNA expression was determined by real-time RT-PCR. Data are showed as mean ± standard deviation (SD) ( n = 8 each group). ∗∗ P < 0.01 versus SD group; △ P < 0.05 and △△ P < 0.01 versus OLETF group. IRS1: insulin receptor substrate 1; IRS2: insulin receptor substrate 2; PI3K: phosphatidylinositol-3 kinase; PKC: protein kinase C; GLUT4: glucose transporter 4; Akt2: protein kinase B beta.

Article Snippet: Nonspecific binding sites were blocked with 5% milk powder diluted in TBS with 0.05% Tween 20 (TBST) for 60 min. Proteins were detected using the following antibodies: rabbit polyclonal antibody for PI3K-p85 (diluted 1 : 3000; Bios; bs-0128R), rabbit polyclonal antibody for phospho-PKC ζ / λ (diluted 1 : 3000; CST; #9378), rabbit polyclonal antibody for GLUT4 (diluted 1 : 3000; Boster; BA1626), and mouse monoclonal antibody for GAPDH (diluted 1 : 3000; Boster; BM1623).

Techniques: Expressing, Quantitative RT-PCR, Standard Deviation

Effects of acupuncture on protein expressions of PI3K-p85, phospho-PKC ζ / λ , and GLUT4 in skeletal muscle of OLETF rats. Protein expression was determined by Western blot. GAPDH was used as an internal control. Data are shown as mean ± SD ( n = 8 each group). ∗ P < 0.05 and ∗∗ P < 0.01 versus SD group; △△ P < 0.01 versus OLETF group.

Journal: Evidence-based Complementary and Alternative Medicine : eCAM

Article Title: Acupuncture Alters Expression of Insulin Signaling Related Molecules and Improves Insulin Resistance in OLETF Rats

doi: 10.1155/2016/9651592

Figure Lengend Snippet: Effects of acupuncture on protein expressions of PI3K-p85, phospho-PKC ζ / λ , and GLUT4 in skeletal muscle of OLETF rats. Protein expression was determined by Western blot. GAPDH was used as an internal control. Data are shown as mean ± SD ( n = 8 each group). ∗ P < 0.05 and ∗∗ P < 0.01 versus SD group; △△ P < 0.01 versus OLETF group.

Article Snippet: Nonspecific binding sites were blocked with 5% milk powder diluted in TBS with 0.05% Tween 20 (TBST) for 60 min. Proteins were detected using the following antibodies: rabbit polyclonal antibody for PI3K-p85 (diluted 1 : 3000; Bios; bs-0128R), rabbit polyclonal antibody for phospho-PKC ζ / λ (diluted 1 : 3000; CST; #9378), rabbit polyclonal antibody for GLUT4 (diluted 1 : 3000; Boster; BA1626), and mouse monoclonal antibody for GAPDH (diluted 1 : 3000; Boster; BM1623).

Techniques: Expressing, Western Blot, Control