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polyclonal antibody against sh3gl1  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology polyclonal antibody against sh3gl1
    Genes identified by SEREX
    Polyclonal Antibody Against Sh3gl1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 60 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/immunohistochemistry+microarray+based+expression+data/Ets+Family+Gel+Shift+Oligonucleotides/pmc03548755-117-3-8
    Average 93 stars, based on 60 article reviews
    polyclonal antibody against sh3gl1 - by Bioz Stars, 2026-10
    93/100 stars

    Images

    1) Product Images from "Autologous antibody to src-homology 3-domain GRB2-like 1 specifically increases in the sera of patients with low-grade gliomas"

    Article Title: Autologous antibody to src-homology 3-domain GRB2-like 1 specifically increases in the sera of patients with low-grade gliomas

    Journal: Journal of Experimental & Clinical Cancer Research : CR

    doi: 10.1186/1756-9966-31-85

    Genes identified by SEREX
    Figure Legend Snippet: Genes identified by SEREX

    Techniques Used: Sequencing, Recombinant, Amplification, Binding Assay, Coagulation, Variant Assay, Migration

    The increasing levels of antibodies to SH3GL1 in sera of the patients with low-grade glioma. Serum antibody level to SH3GL1 was examined by the ELISA as described in the legends of Figure . First screening test (A) and the individual validation test (B) , revealed the significant higher levels of autologous antibody against SH3GL1 in low-grade glioma patients, than healthy donors (P = 0.045 and 0.0189).
    Figure Legend Snippet: The increasing levels of antibodies to SH3GL1 in sera of the patients with low-grade glioma. Serum antibody level to SH3GL1 was examined by the ELISA as described in the legends of Figure . First screening test (A) and the individual validation test (B) , revealed the significant higher levels of autologous antibody against SH3GL1 in low-grade glioma patients, than healthy donors (P = 0.045 and 0.0189).

    Techniques Used: Enzyme-linked Immunosorbent Assay, Biomarker Discovery

    Kaplan-Meier analysis for the overall survival of the patients with low-grade gliomas according to the serum level of anti-SH3GL1 autoantibody. The patients with higher serum level of anti-SH3GL1 autoantibody (solid line) survived significantly longer than those with lower levels (gray line) (p = 0.0124).
    Figure Legend Snippet: Kaplan-Meier analysis for the overall survival of the patients with low-grade gliomas according to the serum level of anti-SH3GL1 autoantibody. The patients with higher serum level of anti-SH3GL1 autoantibody (solid line) survived significantly longer than those with lower levels (gray line) (p = 0.0124).

    Techniques Used:

    Comparison of serum antibody levels among deletion mutants of SH3GL1. To confirm the epitope site, some SH3GL1 deletion mutants (A) were synthesized. Serum antibody levels were examined by ELISA with SH3GL1 muta-1 (B) , mut-2 (C) , mut-3 (D) and mut-4 (E) , and the 10–20 amino acids at the C-terminal end were indicated as the epitope site.
    Figure Legend Snippet: Comparison of serum antibody levels among deletion mutants of SH3GL1. To confirm the epitope site, some SH3GL1 deletion mutants (A) were synthesized. Serum antibody levels were examined by ELISA with SH3GL1 muta-1 (B) , mut-2 (C) , mut-3 (D) and mut-4 (E) , and the 10–20 amino acids at the C-terminal end were indicated as the epitope site.

    Techniques Used: Comparison, Synthesized, Enzyme-linked Immunosorbent Assay

    The detection of epitope site by overlapped peptide array. Series of peptides of 14 amino acid residues, composed of SH3GL1, were synthesized with overlapping by 12 amino acids, and were blotted in nitrocellulose membranes using F-moc amino acids (A) . Three sera of the patients with low-grade glioma indicated the fine reaction in spot 177 and 178 (C) , compared to two normal volunteers (D) and no serum control (B) . The calculated fluorescence intensity, normalized by background control, revealed that these spots were suggested as a minimum epitope site (E).
    Figure Legend Snippet: The detection of epitope site by overlapped peptide array. Series of peptides of 14 amino acid residues, composed of SH3GL1, were synthesized with overlapping by 12 amino acids, and were blotted in nitrocellulose membranes using F-moc amino acids (A) . Three sera of the patients with low-grade glioma indicated the fine reaction in spot 177 and 178 (C) , compared to two normal volunteers (D) and no serum control (B) . The calculated fluorescence intensity, normalized by background control, revealed that these spots were suggested as a minimum epitope site (E).

    Techniques Used: Peptide Microarray, Synthesized, Control, Fluorescence

    Immunohistochemical analysis of SH3GL1 in glioma cells. Immunohistochemical stain for SH3GL1 in whole normal brain, consisted of white matter and gray matter (A) , and three representative results of normal white matter, low-grade glioma and high-grade glioma (B) were shown. Immunostaining for SH3GL1 was classified in five groups, and numbers of tissues in each group were scored (C).
    Figure Legend Snippet: Immunohistochemical analysis of SH3GL1 in glioma cells. Immunohistochemical stain for SH3GL1 in whole normal brain, consisted of white matter and gray matter (A) , and three representative results of normal white matter, low-grade glioma and high-grade glioma (B) were shown. Immunostaining for SH3GL1 was classified in five groups, and numbers of tissues in each group were scored (C).

    Techniques Used: Immunohistochemical staining, Staining, Immunostaining

    Changes in the serum autoantibody level to SH3GL1 in a rat brain tumor model using C6 rat glioblastoma cells which were confirmed to express SH3GL1 protein. MRI studies show a steady growth of tumor mass in the rat brain (A) . The serum autoantibody levels were significantly increased at 2-week after tumor inoculation, and tended to decrease at 4-week after the inoculation (B).
    Figure Legend Snippet: Changes in the serum autoantibody level to SH3GL1 in a rat brain tumor model using C6 rat glioblastoma cells which were confirmed to express SH3GL1 protein. MRI studies show a steady growth of tumor mass in the rat brain (A) . The serum autoantibody levels were significantly increased at 2-week after tumor inoculation, and tended to decrease at 4-week after the inoculation (B).

    Techniques Used:

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    Incubation:

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    Article Snippet: For immunoblotting equivalent amounts of extracts were resolved by SDS–polyacrylamide gel electrophoresis (PAGE), electrotransferred to polyvinylidene fluoride membrane (Millipore, MA), as previously described (Benatti et al., ). .. Membranes were incubated with primary antibodies: anti‐CB2r (1:1,000, sc‐25494, Santa Cruz Biotechnology, Texas), anti‐Vinculin (1:10,000, #V4504, Merck KGaA, Germany) in blocking‐buffer. .. Secondary antibody: anti‐rabbit IgG‐HRP‐linked (1:5,000, #7071, Cell Signaling, MA) for all targets.

    Article Title: Cannabinoid receptors are differentially regulated in the pancreatic islets during the early development of metabolic syndrome
    Article Snippet: .. Primary antibodies were incubated overnight at 4°C as follows: CB1 rabbit polyclonal antibody 1:500 (Cayman Chemical Company, cat 10006590), CB2 rabbit polyclonal antibody 1:500 (Santa Cruz Biotechnology Inc., sc-25494), insulin goat polyclonal antibody 1:500 (Santa Cruz Biotechnology Inc., sc-7839). .. After washing, secondary antibodies were incubated for 2 h at 20°C, AlexaFluor 488 donkey anti-rabbit secondary antibody 1:1000 (Abcam, A-21206) and AlexaFluor 546 donkey anti-goat secondary antibody 1:1000 (Abcam, A-11056).

    Article Title: Electro-acupuncture Pretreatment at Zusanli (ST36) Acupoint Attenuates Lipopolysaccharide-Induced Inflammation in Rats by Inhibiting Ca 2+ Influx Associated with Cannabinoid CB2 Receptors.
    Article Snippet: In this study, we aimed to investigate the effect of electro-acupuncture (EA) pretreatment at zusanli (ST36) acupoint on lipopolysaccharide (LPS)-induced endotoxemic rat model and explore the underlying molecular mechanisms.. Rats were treated with EA at ST36 for 7 days before being subjected to LPS.. Two hours post-LPS, samples such as serum, local acupoint tissues, and spleens were collected and processed for investigations including cytokine production, cytosolic calcium (Ca) concentration, Ca influx, cannabinoid CB2 receptor (CB2R) expression, and TLR4/NF-κB signaling.

    Article Title: Cannabinoid receptors are differentially regulated in the pancreatic islets during the early development of metabolic syndrome
    Article Snippet: The membrane was stained with Ponceau’s S Red and photographed (G12 camera, Canon), and each lane was then cut for subsequent incubation. .. The membrane was washed and incubated with PBS 1X – Tween20 0.3%, 10% nonfat dry milk, and 2% goat normal serum for 30 min at 20°C, and then incubated with anti-CB1 (1:1500; Cayman Chemical Company, cat 10006590), or anti-CB2 (1:500; Santa Cruz Biotechnology, Inc., sc-25494) overnight at 4°C. ..

    Article Title: Neutrophils undergo switch of apoptosis to NETosis during murine fatty liver injury via S1P receptor 2 signaling
    Article Snippet: .. Cells were fixed in 4% paraformaldehyde in PBS for 30 min and permeabilized in 0.5% Triton X-100 in PBS for 3 min; after blocking with 2% bovine serum albumin (Roche), they were incubated with the specific primary antibodies for S1PR 1 (1:50, Santa Cruz, sc-25489); S1PR 2 (1:50, Santa Cruz, sc-25491); S1PR 3 (1:50, Santa Cruz, sc-30024); citrullinated-histone H3 (Cit-H3) (1:200, Abcam), myeloperoxidase (MPO) (1:200; Abcam, 14569), or neutrophil elastase (NE) (1:100, Abcam, ab21595), and secondary antibody conjugated with Cy3 (1:100, Jackson Immunoresearch) was a secondary antibody. .. The samples were observed under a confocal microscope (LSM510, Carl Zeiss MicroImaging).

    Blocking Assay:

    Article Title: Non‐psychotropic Cannabis sativa L. phytocomplex modulates microglial inflammatory response through CB2 receptors‐, endocannabinoids‐, and NF‐κB ‐mediated signaling
    Article Snippet: For immunoblotting equivalent amounts of extracts were resolved by SDS–polyacrylamide gel electrophoresis (PAGE), electrotransferred to polyvinylidene fluoride membrane (Millipore, MA), as previously described (Benatti et al., ). .. Membranes were incubated with primary antibodies: anti‐CB2r (1:1,000, sc‐25494, Santa Cruz Biotechnology, Texas), anti‐Vinculin (1:10,000, #V4504, Merck KGaA, Germany) in blocking‐buffer. .. Secondary antibody: anti‐rabbit IgG‐HRP‐linked (1:5,000, #7071, Cell Signaling, MA) for all targets.

    Article Title: Neutrophils undergo switch of apoptosis to NETosis during murine fatty liver injury via S1P receptor 2 signaling
    Article Snippet: .. Cells were fixed in 4% paraformaldehyde in PBS for 30 min and permeabilized in 0.5% Triton X-100 in PBS for 3 min; after blocking with 2% bovine serum albumin (Roche), they were incubated with the specific primary antibodies for S1PR 1 (1:50, Santa Cruz, sc-25489); S1PR 2 (1:50, Santa Cruz, sc-25491); S1PR 3 (1:50, Santa Cruz, sc-30024); citrullinated-histone H3 (Cit-H3) (1:200, Abcam), myeloperoxidase (MPO) (1:200; Abcam, 14569), or neutrophil elastase (NE) (1:100, Abcam, ab21595), and secondary antibody conjugated with Cy3 (1:100, Jackson Immunoresearch) was a secondary antibody. .. The samples were observed under a confocal microscope (LSM510, Carl Zeiss MicroImaging).

    Western Blot:

    Article Title: Conjugated Bile Acids Promote Invasive Growth of Esophageal Adenocarcinoma Cells and Cancer Stem Cell Expansion via Sphingosine 1-Phosphate Receptor 2–Mediated Yes-Associated Protein Activation
    Article Snippet: All other supplemental materials for cell culture were obtained from Gibco (Thermo Fischer Scientific, Waltham, MA). .. Antibodies used in this study are listed in . table ft1 table-wrap mode="anchored" t5 caption a7 Antibody Species Source Catalog number Application (dilution) S1PR1 Rabbit Abcam (Cambridge, UK) Ab23695 WB (1:500) S1PR2 Rabbit Santa Cruz Biotechnology (Dallas, TX) sc-25491 WB (1:200) S1PR3 Rabbit Santa Cruz Biotechnology sc-30024 WB (1:200) E-cadherin Rabbit Santa Cruz Biotechnology sc-7870 WB (1:200)/IF (1:50) Vimentin Rabbit Cell Signaling Technology (Danvers, MA) mAb 5741 WB (1:1000) CTGF Rabbit Sigma-Aldrich (St. Louis, MO) Sab1300909 WB (1:500) β-Catenin Mouse Santa Cruz Biotechnology sc-7963 WB (1:500) YAP Rabbit Sigma-Aldrich Y0771 WB (1:1000) p-YAP Rabbit Sigma-Aldrich Y4645 WB (1:1000) Lamin B Goat Santa Cruz Biotechnology sc-6216 WB (1:500) β-Actin (JLA20) Mouse DSHB at University of Iowa (Iowa City, IA) JLA20 WB (1:500) Open in a separate window CTGF, connective tissue growth factor; DSHB, Developmental Studies Hybridoma Bank; IF, immunofluorescence; mAb, monoclonal antibody; p-YAP, phosphorylated YAP; S1PR, sphingosine 1-phosphate receptor; WB, Western blotting. ..

    Article Title: Conjugated Bile Acids Promote Invasive Growth of Esophageal Adenocarcinoma Cells and Cancer Stem Cell Expansion via Sphingosine 1-Phosphate Receptor 2–Mediated Yes-Associated Protein Activation
    Article Snippet: S1PR1 , Rabbit , Abcam (Cambridge, UK) , Ab23695 , WB (1:500). .. S1PR2 , Rabbit , Santa Cruz Biotechnology (Dallas, TX) , sc-25491 , WB (1:200). .. S1PR3 , Rabbit , Santa Cruz Biotechnology , sc-30024 , WB (1:200).

    Immunofluorescence:

    Article Title: Conjugated Bile Acids Promote Invasive Growth of Esophageal Adenocarcinoma Cells and Cancer Stem Cell Expansion via Sphingosine 1-Phosphate Receptor 2–Mediated Yes-Associated Protein Activation
    Article Snippet: All other supplemental materials for cell culture were obtained from Gibco (Thermo Fischer Scientific, Waltham, MA). .. Antibodies used in this study are listed in . table ft1 table-wrap mode="anchored" t5 caption a7 Antibody Species Source Catalog number Application (dilution) S1PR1 Rabbit Abcam (Cambridge, UK) Ab23695 WB (1:500) S1PR2 Rabbit Santa Cruz Biotechnology (Dallas, TX) sc-25491 WB (1:200) S1PR3 Rabbit Santa Cruz Biotechnology sc-30024 WB (1:200) E-cadherin Rabbit Santa Cruz Biotechnology sc-7870 WB (1:200)/IF (1:50) Vimentin Rabbit Cell Signaling Technology (Danvers, MA) mAb 5741 WB (1:1000) CTGF Rabbit Sigma-Aldrich (St. Louis, MO) Sab1300909 WB (1:500) β-Catenin Mouse Santa Cruz Biotechnology sc-7963 WB (1:500) YAP Rabbit Sigma-Aldrich Y0771 WB (1:1000) p-YAP Rabbit Sigma-Aldrich Y4645 WB (1:1000) Lamin B Goat Santa Cruz Biotechnology sc-6216 WB (1:500) β-Actin (JLA20) Mouse DSHB at University of Iowa (Iowa City, IA) JLA20 WB (1:500) Open in a separate window CTGF, connective tissue growth factor; DSHB, Developmental Studies Hybridoma Bank; IF, immunofluorescence; mAb, monoclonal antibody; p-YAP, phosphorylated YAP; S1PR, sphingosine 1-phosphate receptor; WB, Western blotting. ..

    Membrane:

    Article Title: Cannabinoid receptors are differentially regulated in the pancreatic islets during the early development of metabolic syndrome
    Article Snippet: The membrane was stained with Ponceau’s S Red and photographed (G12 camera, Canon), and each lane was then cut for subsequent incubation. .. The membrane was washed and incubated with PBS 1X – Tween20 0.3%, 10% nonfat dry milk, and 2% goat normal serum for 30 min at 20°C, and then incubated with anti-CB1 (1:1500; Cayman Chemical Company, cat 10006590), or anti-CB2 (1:500; Santa Cruz Biotechnology, Inc., sc-25494) overnight at 4°C. ..



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