hip sirna  (Santa Cruz Biotechnology)

 
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    Name:
    Hhip siRNA
    Description:
    Gene Silencers generally consist of pools of three to five target specific 19 25 nucleotide sequences in length For independent verification of Hhip gene silencing results individual duplex components or plasmids are also available upon request Suitable control antibody Hhip Antibody 5D11 sc 293265 is recommended as control antibody for monitoring of Hhip expression knockdown by Western blotting or immunofluorescence
    Catalog Number:
    SC-43835
    Price:
    None
    Category:
    Gene Editing siRNA shRNA Gene Silencers Membrane Receptor Hhip siRNA shRNA Plasmid and Lentiviral Particle Gene Silencers Hhip siRNA and shRNA Plasmids h
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    Structured Review

    Santa Cruz Biotechnology hip sirna
    Characterization and consequences of GPC3–lhh interaction. ( A – C ) Ihh binds to GPC3. ( A ) Binding of 125 I-Ihh to human embryonic kidney (HEK)293T cells transfected with GPC3 expressing vector or vector controls (EF). A representative experiment of three is shown: points, average of triplicates; bars, ±s.d. ( B ) The specific binding of 125 I-Ihh to HEK293T cells transfected with GPC3 or EF was determined in the presence of 100 × unlabelled Ihh. Bars: average of triplicates+s.d.; asterisk: statistically significant difference. ( C ) SRP analysis of the GPC3–Ihh interaction. GPC3ΔGPI was immobilized in the flow cell into streptavidin-coated SA sensor chips, and various concentrations of Ihh (bottom to top: 15, 30, 60, 120 and 240 nM) were injected on the surface of flow cells. The nonspecific binding was subtracted from the sensogram. Inset: ka , kd and Kd values were determined using a 1:1 Languimuir binding model. Each value is expressed as the mean±s.e. of five different concentrations. ( D ) GPC3 inhibits Hh signalling independently of CDO and <t>HIP.</t> Top: NIH 3T3 cells were transfected with a GPC3 or EF along with a luciferase reporter vector driven by an Hh responsive promoter (8Xgli) and β-galactosidase. As indicated, <t>siRNA</t> for silencing CDO siRNA, HIP siRNA or non-targeting control siRNA was also transfected. Cells were stimulated for 48 h with Shh- or control-conditioned medium and luciferase and β-galactosidase assays carried out. For each siRNA condition, the fold stimulation induced by Hh in EF-transfected cells was considered to be 100%. Bars represent the luciferase activity as percentage of the control (average+s.d. of triplicates). Bottom: Western blot for CDO and HIP in NIH 3T3 cells treated as indicated, using actin as loading control. ( E , F ) Increased Ihh levels in GPC3-null mice. ( E ) Western blot analysis of Ihh levels in whole-embryo lysates using actin as loading control was carried out. Bands were then scanned and quantified by densitometry. Average density+s.d. of Ihh/actin ratio is shown. In all three independent litters were analysed. ( F ) Relative levels of Ihh transcripts determined by real-time PCR using β-actin transcript levels as reference. Two independent litters were analysed. Bars represent mean+s.d. for the indicated genotypes. CDO, CAM-related/downregulated by oncogenes; EF, elongation factor; GPC3, Glypican 3; Hh, hedgehog; HIP, Hedgehog-interacting protein; Ihh, Indian hedgehog; mRNA, messenger RNA; PCR, polymerase chain reaction; RU, relative units; Shh, sonic hedgehog; siRNA, small interference RNA; SRP, small plasmon resonance; WT, wild type.
    Gene Silencers generally consist of pools of three to five target specific 19 25 nucleotide sequences in length For independent verification of Hhip gene silencing results individual duplex components or plasmids are also available upon request Suitable control antibody Hhip Antibody 5D11 sc 293265 is recommended as control antibody for monitoring of Hhip expression knockdown by Western blotting or immunofluorescence
    https://www.bioz.com/result/hip sirna/product/Santa Cruz Biotechnology
    Average 92 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    hip sirna - by Bioz Stars, 2021-07
    92/100 stars

    Images

    1) Product Images from "Overgrowth of a mouse model of Simpson- Golabi-Behmel syndrome is partly mediated by Indian Hedgehog"

    Article Title: Overgrowth of a mouse model of Simpson- Golabi-Behmel syndrome is partly mediated by Indian Hedgehog

    Journal: EMBO Reports

    doi: 10.1038/embor.2009.98

    Characterization and consequences of GPC3–lhh interaction. ( A – C ) Ihh binds to GPC3. ( A ) Binding of 125 I-Ihh to human embryonic kidney (HEK)293T cells transfected with GPC3 expressing vector or vector controls (EF). A representative experiment of three is shown: points, average of triplicates; bars, ±s.d. ( B ) The specific binding of 125 I-Ihh to HEK293T cells transfected with GPC3 or EF was determined in the presence of 100 × unlabelled Ihh. Bars: average of triplicates+s.d.; asterisk: statistically significant difference. ( C ) SRP analysis of the GPC3–Ihh interaction. GPC3ΔGPI was immobilized in the flow cell into streptavidin-coated SA sensor chips, and various concentrations of Ihh (bottom to top: 15, 30, 60, 120 and 240 nM) were injected on the surface of flow cells. The nonspecific binding was subtracted from the sensogram. Inset: ka , kd and Kd values were determined using a 1:1 Languimuir binding model. Each value is expressed as the mean±s.e. of five different concentrations. ( D ) GPC3 inhibits Hh signalling independently of CDO and HIP. Top: NIH 3T3 cells were transfected with a GPC3 or EF along with a luciferase reporter vector driven by an Hh responsive promoter (8Xgli) and β-galactosidase. As indicated, siRNA for silencing CDO siRNA, HIP siRNA or non-targeting control siRNA was also transfected. Cells were stimulated for 48 h with Shh- or control-conditioned medium and luciferase and β-galactosidase assays carried out. For each siRNA condition, the fold stimulation induced by Hh in EF-transfected cells was considered to be 100%. Bars represent the luciferase activity as percentage of the control (average+s.d. of triplicates). Bottom: Western blot for CDO and HIP in NIH 3T3 cells treated as indicated, using actin as loading control. ( E , F ) Increased Ihh levels in GPC3-null mice. ( E ) Western blot analysis of Ihh levels in whole-embryo lysates using actin as loading control was carried out. Bands were then scanned and quantified by densitometry. Average density+s.d. of Ihh/actin ratio is shown. In all three independent litters were analysed. ( F ) Relative levels of Ihh transcripts determined by real-time PCR using β-actin transcript levels as reference. Two independent litters were analysed. Bars represent mean+s.d. for the indicated genotypes. CDO, CAM-related/downregulated by oncogenes; EF, elongation factor; GPC3, Glypican 3; Hh, hedgehog; HIP, Hedgehog-interacting protein; Ihh, Indian hedgehog; mRNA, messenger RNA; PCR, polymerase chain reaction; RU, relative units; Shh, sonic hedgehog; siRNA, small interference RNA; SRP, small plasmon resonance; WT, wild type.
    Figure Legend Snippet: Characterization and consequences of GPC3–lhh interaction. ( A – C ) Ihh binds to GPC3. ( A ) Binding of 125 I-Ihh to human embryonic kidney (HEK)293T cells transfected with GPC3 expressing vector or vector controls (EF). A representative experiment of three is shown: points, average of triplicates; bars, ±s.d. ( B ) The specific binding of 125 I-Ihh to HEK293T cells transfected with GPC3 or EF was determined in the presence of 100 × unlabelled Ihh. Bars: average of triplicates+s.d.; asterisk: statistically significant difference. ( C ) SRP analysis of the GPC3–Ihh interaction. GPC3ΔGPI was immobilized in the flow cell into streptavidin-coated SA sensor chips, and various concentrations of Ihh (bottom to top: 15, 30, 60, 120 and 240 nM) were injected on the surface of flow cells. The nonspecific binding was subtracted from the sensogram. Inset: ka , kd and Kd values were determined using a 1:1 Languimuir binding model. Each value is expressed as the mean±s.e. of five different concentrations. ( D ) GPC3 inhibits Hh signalling independently of CDO and HIP. Top: NIH 3T3 cells were transfected with a GPC3 or EF along with a luciferase reporter vector driven by an Hh responsive promoter (8Xgli) and β-galactosidase. As indicated, siRNA for silencing CDO siRNA, HIP siRNA or non-targeting control siRNA was also transfected. Cells were stimulated for 48 h with Shh- or control-conditioned medium and luciferase and β-galactosidase assays carried out. For each siRNA condition, the fold stimulation induced by Hh in EF-transfected cells was considered to be 100%. Bars represent the luciferase activity as percentage of the control (average+s.d. of triplicates). Bottom: Western blot for CDO and HIP in NIH 3T3 cells treated as indicated, using actin as loading control. ( E , F ) Increased Ihh levels in GPC3-null mice. ( E ) Western blot analysis of Ihh levels in whole-embryo lysates using actin as loading control was carried out. Bands were then scanned and quantified by densitometry. Average density+s.d. of Ihh/actin ratio is shown. In all three independent litters were analysed. ( F ) Relative levels of Ihh transcripts determined by real-time PCR using β-actin transcript levels as reference. Two independent litters were analysed. Bars represent mean+s.d. for the indicated genotypes. CDO, CAM-related/downregulated by oncogenes; EF, elongation factor; GPC3, Glypican 3; Hh, hedgehog; HIP, Hedgehog-interacting protein; Ihh, Indian hedgehog; mRNA, messenger RNA; PCR, polymerase chain reaction; RU, relative units; Shh, sonic hedgehog; siRNA, small interference RNA; SRP, small plasmon resonance; WT, wild type.

    Techniques Used: Binding Assay, Transfection, Expressing, Plasmid Preparation, Flow Cytometry, Injection, Luciferase, Activity Assay, Western Blot, Mouse Assay, Real-time Polymerase Chain Reaction, Chick Chorioallantoic Membrane Assay, Polymerase Chain Reaction

    Related Articles

    Transfection:

    Article Title: Overgrowth of a mouse model of Simpson- Golabi-Behmel syndrome is partly mediated by Indian Hedgehog
    Article Snippet: The Gli reporter assay was carried out in NIH 3T3 cells as described previously ( ). .. To silence CDO or HIP, 100 nM of CDO siRNA (sc-60346, Santa Cruz), HIP siRNA (sc-40164, Santa Cruz) or non-targeting control siRNA A (sc-37007, Santa Cruz) was transfected using DharmaFECT-1 transfection reagent (Dharmacon, Chicago, IL, USA). β-Galactosidase activity was used to normalize the transfection efficiencies. .. For each siRNA condition, results are presented as a percentage of the luciferase activity measured after transfection with vector control (elongation factor (EF)). siRNA-mediated knockdown of CDO and HIP was confirmed in parallel wells by Western blot analysis.

    Activity Assay:

    Article Title: Overgrowth of a mouse model of Simpson- Golabi-Behmel syndrome is partly mediated by Indian Hedgehog
    Article Snippet: The Gli reporter assay was carried out in NIH 3T3 cells as described previously ( ). .. To silence CDO or HIP, 100 nM of CDO siRNA (sc-60346, Santa Cruz), HIP siRNA (sc-40164, Santa Cruz) or non-targeting control siRNA A (sc-37007, Santa Cruz) was transfected using DharmaFECT-1 transfection reagent (Dharmacon, Chicago, IL, USA). β-Galactosidase activity was used to normalize the transfection efficiencies. .. For each siRNA condition, results are presented as a percentage of the luciferase activity measured after transfection with vector control (elongation factor (EF)). siRNA-mediated knockdown of CDO and HIP was confirmed in parallel wells by Western blot analysis.

    Small Interfering RNA:

    Article Title: Hedgehog Interacting Protein (Hhip) Regulates Insulin Secretion in Mice Fed High Fat Diets
    Article Snippet: Mouse anti-gp91phox-Cter for WB (1:10000) was obtained from Dr. Nathalie Grandvaux (CRCHUM) as reported elsewhere . .. Chemical reagents included small interfering RNA (siRNA) of Hhip from Santa Cruz Biotechnology (Santa Cruz, CA, USA), which pools three target-specific 19–25 nucleotide sequences (Fig. ); recombinant Hhip (rHhip) from R & D Systems, Inc. (Burlington, ON, Canada); BSA (fatty acid free) and sodium palmitate (PA) were procured from Sigma-Aldrich Canada. ..

    Recombinant:

    Article Title: Hedgehog Interacting Protein (Hhip) Regulates Insulin Secretion in Mice Fed High Fat Diets
    Article Snippet: Mouse anti-gp91phox-Cter for WB (1:10000) was obtained from Dr. Nathalie Grandvaux (CRCHUM) as reported elsewhere . .. Chemical reagents included small interfering RNA (siRNA) of Hhip from Santa Cruz Biotechnology (Santa Cruz, CA, USA), which pools three target-specific 19–25 nucleotide sequences (Fig. ); recombinant Hhip (rHhip) from R & D Systems, Inc. (Burlington, ON, Canada); BSA (fatty acid free) and sodium palmitate (PA) were procured from Sigma-Aldrich Canada. ..

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  • 92
    Santa Cruz Biotechnology hip sirna
    Characterization and consequences of GPC3–lhh interaction. ( A – C ) Ihh binds to GPC3. ( A ) Binding of 125 I-Ihh to human embryonic kidney (HEK)293T cells transfected with GPC3 expressing vector or vector controls (EF). A representative experiment of three is shown: points, average of triplicates; bars, ±s.d. ( B ) The specific binding of 125 I-Ihh to HEK293T cells transfected with GPC3 or EF was determined in the presence of 100 × unlabelled Ihh. Bars: average of triplicates+s.d.; asterisk: statistically significant difference. ( C ) SRP analysis of the GPC3–Ihh interaction. GPC3ΔGPI was immobilized in the flow cell into streptavidin-coated SA sensor chips, and various concentrations of Ihh (bottom to top: 15, 30, 60, 120 and 240 nM) were injected on the surface of flow cells. The nonspecific binding was subtracted from the sensogram. Inset: ka , kd and Kd values were determined using a 1:1 Languimuir binding model. Each value is expressed as the mean±s.e. of five different concentrations. ( D ) GPC3 inhibits Hh signalling independently of CDO and <t>HIP.</t> Top: NIH 3T3 cells were transfected with a GPC3 or EF along with a luciferase reporter vector driven by an Hh responsive promoter (8Xgli) and β-galactosidase. As indicated, <t>siRNA</t> for silencing CDO siRNA, HIP siRNA or non-targeting control siRNA was also transfected. Cells were stimulated for 48 h with Shh- or control-conditioned medium and luciferase and β-galactosidase assays carried out. For each siRNA condition, the fold stimulation induced by Hh in EF-transfected cells was considered to be 100%. Bars represent the luciferase activity as percentage of the control (average+s.d. of triplicates). Bottom: Western blot for CDO and HIP in NIH 3T3 cells treated as indicated, using actin as loading control. ( E , F ) Increased Ihh levels in GPC3-null mice. ( E ) Western blot analysis of Ihh levels in whole-embryo lysates using actin as loading control was carried out. Bands were then scanned and quantified by densitometry. Average density+s.d. of Ihh/actin ratio is shown. In all three independent litters were analysed. ( F ) Relative levels of Ihh transcripts determined by real-time PCR using β-actin transcript levels as reference. Two independent litters were analysed. Bars represent mean+s.d. for the indicated genotypes. CDO, CAM-related/downregulated by oncogenes; EF, elongation factor; GPC3, Glypican 3; Hh, hedgehog; HIP, Hedgehog-interacting protein; Ihh, Indian hedgehog; mRNA, messenger RNA; PCR, polymerase chain reaction; RU, relative units; Shh, sonic hedgehog; siRNA, small interference RNA; SRP, small plasmon resonance; WT, wild type.
    Hip Sirna, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/hip sirna/product/Santa Cruz Biotechnology
    Average 92 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    hip sirna - by Bioz Stars, 2021-07
    92/100 stars
      Buy from Supplier

    85
    Santa Cruz Biotechnology st13 knockdown
    Effect of <t>ST13</t> expression on SW620 cell cycling
    St13 Knockdown, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/st13 knockdown/product/Santa Cruz Biotechnology
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    85
    Santa Cruz Biotechnology sirnas
    Effect of <t>ST13</t> expression on SW620 cell cycling
    Sirnas, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Santa Cruz Biotechnology hip 55 shrna plasmid
    Effect of <t>ST13</t> expression on SW620 cell cycling
    Hip 55 Shrna Plasmid, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/hip 55 shrna plasmid/product/Santa Cruz Biotechnology
    Average 92 stars, based on 1 article reviews
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    Image Search Results


    Characterization and consequences of GPC3–lhh interaction. ( A – C ) Ihh binds to GPC3. ( A ) Binding of 125 I-Ihh to human embryonic kidney (HEK)293T cells transfected with GPC3 expressing vector or vector controls (EF). A representative experiment of three is shown: points, average of triplicates; bars, ±s.d. ( B ) The specific binding of 125 I-Ihh to HEK293T cells transfected with GPC3 or EF was determined in the presence of 100 × unlabelled Ihh. Bars: average of triplicates+s.d.; asterisk: statistically significant difference. ( C ) SRP analysis of the GPC3–Ihh interaction. GPC3ΔGPI was immobilized in the flow cell into streptavidin-coated SA sensor chips, and various concentrations of Ihh (bottom to top: 15, 30, 60, 120 and 240 nM) were injected on the surface of flow cells. The nonspecific binding was subtracted from the sensogram. Inset: ka , kd and Kd values were determined using a 1:1 Languimuir binding model. Each value is expressed as the mean±s.e. of five different concentrations. ( D ) GPC3 inhibits Hh signalling independently of CDO and HIP. Top: NIH 3T3 cells were transfected with a GPC3 or EF along with a luciferase reporter vector driven by an Hh responsive promoter (8Xgli) and β-galactosidase. As indicated, siRNA for silencing CDO siRNA, HIP siRNA or non-targeting control siRNA was also transfected. Cells were stimulated for 48 h with Shh- or control-conditioned medium and luciferase and β-galactosidase assays carried out. For each siRNA condition, the fold stimulation induced by Hh in EF-transfected cells was considered to be 100%. Bars represent the luciferase activity as percentage of the control (average+s.d. of triplicates). Bottom: Western blot for CDO and HIP in NIH 3T3 cells treated as indicated, using actin as loading control. ( E , F ) Increased Ihh levels in GPC3-null mice. ( E ) Western blot analysis of Ihh levels in whole-embryo lysates using actin as loading control was carried out. Bands were then scanned and quantified by densitometry. Average density+s.d. of Ihh/actin ratio is shown. In all three independent litters were analysed. ( F ) Relative levels of Ihh transcripts determined by real-time PCR using β-actin transcript levels as reference. Two independent litters were analysed. Bars represent mean+s.d. for the indicated genotypes. CDO, CAM-related/downregulated by oncogenes; EF, elongation factor; GPC3, Glypican 3; Hh, hedgehog; HIP, Hedgehog-interacting protein; Ihh, Indian hedgehog; mRNA, messenger RNA; PCR, polymerase chain reaction; RU, relative units; Shh, sonic hedgehog; siRNA, small interference RNA; SRP, small plasmon resonance; WT, wild type.

    Journal: EMBO Reports

    Article Title: Overgrowth of a mouse model of Simpson- Golabi-Behmel syndrome is partly mediated by Indian Hedgehog

    doi: 10.1038/embor.2009.98

    Figure Lengend Snippet: Characterization and consequences of GPC3–lhh interaction. ( A – C ) Ihh binds to GPC3. ( A ) Binding of 125 I-Ihh to human embryonic kidney (HEK)293T cells transfected with GPC3 expressing vector or vector controls (EF). A representative experiment of three is shown: points, average of triplicates; bars, ±s.d. ( B ) The specific binding of 125 I-Ihh to HEK293T cells transfected with GPC3 or EF was determined in the presence of 100 × unlabelled Ihh. Bars: average of triplicates+s.d.; asterisk: statistically significant difference. ( C ) SRP analysis of the GPC3–Ihh interaction. GPC3ΔGPI was immobilized in the flow cell into streptavidin-coated SA sensor chips, and various concentrations of Ihh (bottom to top: 15, 30, 60, 120 and 240 nM) were injected on the surface of flow cells. The nonspecific binding was subtracted from the sensogram. Inset: ka , kd and Kd values were determined using a 1:1 Languimuir binding model. Each value is expressed as the mean±s.e. of five different concentrations. ( D ) GPC3 inhibits Hh signalling independently of CDO and HIP. Top: NIH 3T3 cells were transfected with a GPC3 or EF along with a luciferase reporter vector driven by an Hh responsive promoter (8Xgli) and β-galactosidase. As indicated, siRNA for silencing CDO siRNA, HIP siRNA or non-targeting control siRNA was also transfected. Cells were stimulated for 48 h with Shh- or control-conditioned medium and luciferase and β-galactosidase assays carried out. For each siRNA condition, the fold stimulation induced by Hh in EF-transfected cells was considered to be 100%. Bars represent the luciferase activity as percentage of the control (average+s.d. of triplicates). Bottom: Western blot for CDO and HIP in NIH 3T3 cells treated as indicated, using actin as loading control. ( E , F ) Increased Ihh levels in GPC3-null mice. ( E ) Western blot analysis of Ihh levels in whole-embryo lysates using actin as loading control was carried out. Bands were then scanned and quantified by densitometry. Average density+s.d. of Ihh/actin ratio is shown. In all three independent litters were analysed. ( F ) Relative levels of Ihh transcripts determined by real-time PCR using β-actin transcript levels as reference. Two independent litters were analysed. Bars represent mean+s.d. for the indicated genotypes. CDO, CAM-related/downregulated by oncogenes; EF, elongation factor; GPC3, Glypican 3; Hh, hedgehog; HIP, Hedgehog-interacting protein; Ihh, Indian hedgehog; mRNA, messenger RNA; PCR, polymerase chain reaction; RU, relative units; Shh, sonic hedgehog; siRNA, small interference RNA; SRP, small plasmon resonance; WT, wild type.

    Article Snippet: To silence CDO or HIP, 100 nM of CDO siRNA (sc-60346, Santa Cruz), HIP siRNA (sc-40164, Santa Cruz) or non-targeting control siRNA A (sc-37007, Santa Cruz) was transfected using DharmaFECT-1 transfection reagent (Dharmacon, Chicago, IL, USA). β-Galactosidase activity was used to normalize the transfection efficiencies.

    Techniques: Binding Assay, Transfection, Expressing, Plasmid Preparation, Flow Cytometry, Injection, Luciferase, Activity Assay, Western Blot, Mouse Assay, Real-time Polymerase Chain Reaction, Chick Chorioallantoic Membrane Assay, Polymerase Chain Reaction

    Effect of ST13 expression on SW620 cell cycling

    Journal: Journal of Zhejiang University. Science. B

    Article Title: ST13, a proliferation regulator, inhibits growth and migration of colorectal cancer cell lines *

    doi: 10.1631/jzus.B1200037

    Figure Lengend Snippet: Effect of ST13 expression on SW620 cell cycling

    Article Snippet: Small hairpin RNA (shRNA) lentiviral particles used for ST13 knockdown (sc-40684-v) and Mock knockdown (sc-108080) were purchased from Santa Cruz, CA, USA.

    Techniques: Expressing

    Effect of ST13 expression on SW620 cell growth in vitro

    Journal: Journal of Zhejiang University. Science. B

    Article Title: ST13, a proliferation regulator, inhibits growth and migration of colorectal cancer cell lines *

    doi: 10.1631/jzus.B1200037

    Figure Lengend Snippet: Effect of ST13 expression on SW620 cell growth in vitro

    Article Snippet: Small hairpin RNA (shRNA) lentiviral particles used for ST13 knockdown (sc-40684-v) and Mock knockdown (sc-108080) were purchased from Santa Cruz, CA, USA.

    Techniques: Expressing, In Vitro

    ST13 expression in colorectal cancer cell lines

    Journal: Journal of Zhejiang University. Science. B

    Article Title: ST13, a proliferation regulator, inhibits growth and migration of colorectal cancer cell lines *

    doi: 10.1631/jzus.B1200037

    Figure Lengend Snippet: ST13 expression in colorectal cancer cell lines

    Article Snippet: Small hairpin RNA (shRNA) lentiviral particles used for ST13 knockdown (sc-40684-v) and Mock knockdown (sc-108080) were purchased from Santa Cruz, CA, USA.

    Techniques: Expressing

    Effect of ST13 expression on SW620 cells migration in vitro

    Journal: Journal of Zhejiang University. Science. B

    Article Title: ST13, a proliferation regulator, inhibits growth and migration of colorectal cancer cell lines *

    doi: 10.1631/jzus.B1200037

    Figure Lengend Snippet: Effect of ST13 expression on SW620 cells migration in vitro

    Article Snippet: Small hairpin RNA (shRNA) lentiviral particles used for ST13 knockdown (sc-40684-v) and Mock knockdown (sc-108080) were purchased from Santa Cruz, CA, USA.

    Techniques: Expressing, Migration, In Vitro

    Effect of ST13 expression on the development and growth of inoculated SW620 cells

    Journal: Journal of Zhejiang University. Science. B

    Article Title: ST13, a proliferation regulator, inhibits growth and migration of colorectal cancer cell lines *

    doi: 10.1631/jzus.B1200037

    Figure Lengend Snippet: Effect of ST13 expression on the development and growth of inoculated SW620 cells

    Article Snippet: Small hairpin RNA (shRNA) lentiviral particles used for ST13 knockdown (sc-40684-v) and Mock knockdown (sc-108080) were purchased from Santa Cruz, CA, USA.

    Techniques: Expressing