sorcin sirna Search Results


sorcin sirna  (Santa Cruz Biotechnology)
88
Santa Cruz Biotechnology sorcin sirna
Figure 1: Expression of <t>sorcin</t> during the period of early pregnancy and during estrous cycle in mouse
Sorcin Sirna, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sorcin+sirna/sorcin+siRNA/10__1530_slash_jme___17___0153-50-26-29
Average 88 stars, based on 1 article reviews
sorcin sirna - by Bioz Stars, 2026-10
88/100 stars
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control lentiviral particles  (Santa Cruz Biotechnology)
90
Santa Cruz Biotechnology control lentiviral particles
Figure 1: Expression of <t>sorcin</t> during the period of early pregnancy and during estrous cycle in mouse
Control Lentiviral Particles, supplied by Santa Cruz Biotechnology, 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/sorcin+sirna/sorcin+shRNA+(h)+Lentiviral+Particles/pmc03282809-52-35-38
Average 90 stars, based on 1 article reviews
control lentiviral particles - by Bioz Stars, 2026-10
90/100 stars
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sorcin  (Santa Cruz Biotechnology)
90
Santa Cruz Biotechnology sorcin
<t>Sorcin</t> controls ChREBP subcellular location in primary mouse β-cells. A : Dissociated mouse islets were transduced for 48 h with null or sorcin-overexpressing adenoviruses in 11 mmol/L glucose RPMI 1640, and then incubated 1 h in 3 mmol/L glucose followed by 6 h in 17 mmol/L RPMI 1640, before immunochemistry and confocal imaging as described in . Scale bars = 5 μm. C : Dissociated mouse islets were transduced with control or sorcin-shRNA lentiviruses for 72 h in 11 mmol/L RPMI 1640 and then incubated for 6 h in 3 mmol/L RPMI 1640 before immunochemistry and confocal imaging as above. B and C : Quantification of endogenous ChREBP in the nucleus, for the experiments presented in A and C . The intensities of ChREBP staining were measured using Volocity 4.0 software, for both nuclear and cytoplasmic regions of interest, in each individual cell, and background intensities were subtracted. Nuclear ChREBP intensity is expressed as percentage of cytoplasmic intensity ( n = 3 experiments, with 24 to 29 cells per condition). (A high-quality digital representation of this figure is available in the online issue.)
Sorcin, supplied by Santa Cruz Biotechnology, 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/sorcin+sirna/sorcin+shRNA+(m)+Lentiviral+Particles/pmc03282809-15-9-23
Average 90 stars, based on 1 article reviews
sorcin - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier
21-nucleotide sirna duplex targeting human sorcin  (Shanghai GenePharma)
90
Shanghai GenePharma 21-nucleotide sirna duplex targeting human sorcin
<t>Sorcin</t> controls ChREBP subcellular location in primary mouse β-cells. A : Dissociated mouse islets were transduced for 48 h with null or sorcin-overexpressing adenoviruses in 11 mmol/L glucose RPMI 1640, and then incubated 1 h in 3 mmol/L glucose followed by 6 h in 17 mmol/L RPMI 1640, before immunochemistry and confocal imaging as described in . Scale bars = 5 μm. C : Dissociated mouse islets were transduced with control or sorcin-shRNA lentiviruses for 72 h in 11 mmol/L RPMI 1640 and then incubated for 6 h in 3 mmol/L RPMI 1640 before immunochemistry and confocal imaging as above. B and C : Quantification of endogenous ChREBP in the nucleus, for the experiments presented in A and C . The intensities of ChREBP staining were measured using Volocity 4.0 software, for both nuclear and cytoplasmic regions of interest, in each individual cell, and background intensities were subtracted. Nuclear ChREBP intensity is expressed as percentage of cytoplasmic intensity ( n = 3 experiments, with 24 to 29 cells per condition). (A high-quality digital representation of this figure is available in the online issue.)
21 Nucleotide Sirna Duplex Targeting Human Sorcin, supplied by Shanghai GenePharma, 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/sorcin+sirna/21+nucleotide+sirna+duplex+targeting+human+sorcin/pm24337682-44-2-27
Average 90 stars, based on 1 article reviews
21-nucleotide sirna duplex targeting human sorcin - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier

Image Search Results


Figure 1: Expression of sorcin during the period of early pregnancy and during estrous cycle in mouse

Journal: Journal of Molecular Endocrinology

Article Title: Sorcin is involved during embryo implantation via activating VEGF/PI3K/Akt pathway in mice

doi: 10.1530/jme-17-0153

Figure Lengend Snippet: Figure 1: Expression of sorcin during the period of early pregnancy and during estrous cycle in mouse

Article Snippet: 128 129 2.4 In vivo sorcin knock-down 130 Pregnant female mice underwent mini laparotomy under anesthesia on D3 of pregnancy to 131 deliver 50 nM of sorcin siRNA (sc-41017; Santa Cruz, CA) in a final volume of 25 μl with 132 Lipofectamine® RNAiMAX reagent (Thermo Fisher Scientific) per manufacturer’s 133 instructions in one of the uterine horn.

Techniques: Expressing

Figure 2: Immunohistochemistry of sorcin expression in mouse uteri during early pregnancy. Sorcin expression was measured in endometrium i.e. glandular epithelium (GE), luminal epithelium (LE), and stroma (S) at different days of pregnancy (D1, D4, D5, D6 and D7). Graph in lower panel shows image score analysis. IS, implantation site; NP, non-pregnant; NC, Negative control. p values are ap<0.001 vs.

Journal: Journal of Molecular Endocrinology

Article Title: Sorcin is involved during embryo implantation via activating VEGF/PI3K/Akt pathway in mice

doi: 10.1530/jme-17-0153

Figure Lengend Snippet: Figure 2: Immunohistochemistry of sorcin expression in mouse uteri during early pregnancy. Sorcin expression was measured in endometrium i.e. glandular epithelium (GE), luminal epithelium (LE), and stroma (S) at different days of pregnancy (D1, D4, D5, D6 and D7). Graph in lower panel shows image score analysis. IS, implantation site; NP, non-pregnant; NC, Negative control. p values are ap<0.001 vs.

Article Snippet: 128 129 2.4 In vivo sorcin knock-down 130 Pregnant female mice underwent mini laparotomy under anesthesia on D3 of pregnancy to 131 deliver 50 nM of sorcin siRNA (sc-41017; Santa Cruz, CA) in a final volume of 25 μl with 132 Lipofectamine® RNAiMAX reagent (Thermo Fisher Scientific) per manufacturer’s 133 instructions in one of the uterine horn.

Techniques: Immunohistochemistry, Expressing, Negative Control

Figure 3: Effect of sorcin inhibition on the number of implantation sites. The right horn was injected with

Journal: Journal of Molecular Endocrinology

Article Title: Sorcin is involved during embryo implantation via activating VEGF/PI3K/Akt pathway in mice

doi: 10.1530/jme-17-0153

Figure Lengend Snippet: Figure 3: Effect of sorcin inhibition on the number of implantation sites. The right horn was injected with

Article Snippet: 128 129 2.4 In vivo sorcin knock-down 130 Pregnant female mice underwent mini laparotomy under anesthesia on D3 of pregnancy to 131 deliver 50 nM of sorcin siRNA (sc-41017; Santa Cruz, CA) in a final volume of 25 μl with 132 Lipofectamine® RNAiMAX reagent (Thermo Fisher Scientific) per manufacturer’s 133 instructions in one of the uterine horn.

Techniques: Inhibition, Injection

Figure 5: Role of ovarian hormones in regulation of sorcin expression. (A) Ovariectomized mice treated with

Journal: Journal of Molecular Endocrinology

Article Title: Sorcin is involved during embryo implantation via activating VEGF/PI3K/Akt pathway in mice

doi: 10.1530/jme-17-0153

Figure Lengend Snippet: Figure 5: Role of ovarian hormones in regulation of sorcin expression. (A) Ovariectomized mice treated with

Article Snippet: 128 129 2.4 In vivo sorcin knock-down 130 Pregnant female mice underwent mini laparotomy under anesthesia on D3 of pregnancy to 131 deliver 50 nM of sorcin siRNA (sc-41017; Santa Cruz, CA) in a final volume of 25 μl with 132 Lipofectamine® RNAiMAX reagent (Thermo Fisher Scientific) per manufacturer’s 133 instructions in one of the uterine horn.

Techniques: Expressing

Figure 6: Effect of sorcin silencing on cytosolic free Ca+2 , VEGF level, VEGFR-2 expression in mouse

Journal: Journal of Molecular Endocrinology

Article Title: Sorcin is involved during embryo implantation via activating VEGF/PI3K/Akt pathway in mice

doi: 10.1530/jme-17-0153

Figure Lengend Snippet: Figure 6: Effect of sorcin silencing on cytosolic free Ca+2 , VEGF level, VEGFR-2 expression in mouse

Article Snippet: 128 129 2.4 In vivo sorcin knock-down 130 Pregnant female mice underwent mini laparotomy under anesthesia on D3 of pregnancy to 131 deliver 50 nM of sorcin siRNA (sc-41017; Santa Cruz, CA) in a final volume of 25 μl with 132 Lipofectamine® RNAiMAX reagent (Thermo Fisher Scientific) per manufacturer’s 133 instructions in one of the uterine horn.

Techniques: Expressing

Figure 7: The proliferation, migration and invasion assay of HUVEC cells. (A) The proliferation of HUVECs was detected in various groups; HUVECs were cultured with supernatants (20% V/V) from mouse primary EECs transfected with sorcin siRNA or scrambled siRNA. In additional group, a blocking anti-VEGF antibody was added in the supernatant from scrambled siRNA treated EECs. Details have been given in “materials and

Journal: Journal of Molecular Endocrinology

Article Title: Sorcin is involved during embryo implantation via activating VEGF/PI3K/Akt pathway in mice

doi: 10.1530/jme-17-0153

Figure Lengend Snippet: Figure 7: The proliferation, migration and invasion assay of HUVEC cells. (A) The proliferation of HUVECs was detected in various groups; HUVECs were cultured with supernatants (20% V/V) from mouse primary EECs transfected with sorcin siRNA or scrambled siRNA. In additional group, a blocking anti-VEGF antibody was added in the supernatant from scrambled siRNA treated EECs. Details have been given in “materials and

Article Snippet: 128 129 2.4 In vivo sorcin knock-down 130 Pregnant female mice underwent mini laparotomy under anesthesia on D3 of pregnancy to 131 deliver 50 nM of sorcin siRNA (sc-41017; Santa Cruz, CA) in a final volume of 25 μl with 132 Lipofectamine® RNAiMAX reagent (Thermo Fisher Scientific) per manufacturer’s 133 instructions in one of the uterine horn.

Techniques: Migration, Invasion Assay, Cell Culture, Transfection, Blocking Assay

Figure 8: Schematic hypothetical representation of the molecular mechanism of sorcin in endometrium

Journal: Journal of Molecular Endocrinology

Article Title: Sorcin is involved during embryo implantation via activating VEGF/PI3K/Akt pathway in mice

doi: 10.1530/jme-17-0153

Figure Lengend Snippet: Figure 8: Schematic hypothetical representation of the molecular mechanism of sorcin in endometrium

Article Snippet: 128 129 2.4 In vivo sorcin knock-down 130 Pregnant female mice underwent mini laparotomy under anesthesia on D3 of pregnancy to 131 deliver 50 nM of sorcin siRNA (sc-41017; Santa Cruz, CA) in a final volume of 25 μl with 132 Lipofectamine® RNAiMAX reagent (Thermo Fisher Scientific) per manufacturer’s 133 instructions in one of the uterine horn.

Techniques:

Sorcin controls ChREBP subcellular location in primary mouse β-cells. A : Dissociated mouse islets were transduced for 48 h with null or sorcin-overexpressing adenoviruses in 11 mmol/L glucose RPMI 1640, and then incubated 1 h in 3 mmol/L glucose followed by 6 h in 17 mmol/L RPMI 1640, before immunochemistry and confocal imaging as described in . Scale bars = 5 μm. C : Dissociated mouse islets were transduced with control or sorcin-shRNA lentiviruses for 72 h in 11 mmol/L RPMI 1640 and then incubated for 6 h in 3 mmol/L RPMI 1640 before immunochemistry and confocal imaging as above. B and C : Quantification of endogenous ChREBP in the nucleus, for the experiments presented in A and C . The intensities of ChREBP staining were measured using Volocity 4.0 software, for both nuclear and cytoplasmic regions of interest, in each individual cell, and background intensities were subtracted. Nuclear ChREBP intensity is expressed as percentage of cytoplasmic intensity ( n = 3 experiments, with 24 to 29 cells per condition). (A high-quality digital representation of this figure is available in the online issue.)

Journal: Diabetes

Article Title: Glucose-Induced Nuclear Shuttling of ChREBP Is Mediated by Sorcin and Ca 2+ Ions in Pancreatic β-Cells

doi: 10.2337/db10-1329

Figure Lengend Snippet: Sorcin controls ChREBP subcellular location in primary mouse β-cells. A : Dissociated mouse islets were transduced for 48 h with null or sorcin-overexpressing adenoviruses in 11 mmol/L glucose RPMI 1640, and then incubated 1 h in 3 mmol/L glucose followed by 6 h in 17 mmol/L RPMI 1640, before immunochemistry and confocal imaging as described in . Scale bars = 5 μm. C : Dissociated mouse islets were transduced with control or sorcin-shRNA lentiviruses for 72 h in 11 mmol/L RPMI 1640 and then incubated for 6 h in 3 mmol/L RPMI 1640 before immunochemistry and confocal imaging as above. B and C : Quantification of endogenous ChREBP in the nucleus, for the experiments presented in A and C . The intensities of ChREBP staining were measured using Volocity 4.0 software, for both nuclear and cytoplasmic regions of interest, in each individual cell, and background intensities were subtracted. Nuclear ChREBP intensity is expressed as percentage of cytoplasmic intensity ( n = 3 experiments, with 24 to 29 cells per condition). (A high-quality digital representation of this figure is available in the online issue.)

Article Snippet: Adenovirus production was then performed as in Ref. . Sorcin (sc-41017-v) and control (sc-108080) short hairpin RNA (shRNA) mouse lentiviruses were purchased from Santa Cruz.

Techniques: Incubation, Imaging, Transduction, Control, shRNA, Staining, Software