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biotin sba  (Vector Laboratories)


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    Structured Review

    Vector Laboratories biotin sba
    Biotin Sba, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 93/100, based on 53 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/B-1015-5/Biotinylated+Soybean+Agglutinin+(SBA)/pm42878060-206-14-15
    Average 93 stars, based on 53 article reviews
    biotin sba - by Bioz Stars, 2026-11
    93/100 stars

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    Related Articles

    Binding Assay:

    Article Title: Ligand-specific tuning of CLEC10A signalling strength and dendritic cell responses through engagement of different GalNAc-containing glycan structures.
    Article Snippet: See the T erm s and C onditions (https://onlinelibrary.w iley.com /term s-and-conditions) on W iley O nline L ibrary for rules of use; O A articles are governed by the applicable C reative C om m ons L icense acetic acid (Fluka, Charlotte, NC, USA/Sigma-Aldrich) in DMSO and incubated for 2 h at 37° C. Subsequently, glycodendrimers were separated from unbound oligosaccharides on PD10 desalting columns (Sigma-Aldrich) according to the manufacturer’s protocol and lyophilised at least five times to improve purity. .. To determine the lectin binding, glycodendrimers were serially diluted in 0.2 M NaHCO3 (Sigma-Aldrich; pH 9.2) and coated onto NUNC Maxisorp plates (Thermo Fisher, Waltham, MA, USA) overnight at 4° C. Plates were blocked with TSM (20 mM Tris, 150 mM NaCl, 2 mM MgCl2 (all Sigma-Aldrich) and 1 mM CaCl2 (VWR chemicals, Radnor, PA, USA)), containing 0.5% bovine serum albumin (BSA fraction V, Roche, Basel, Switzerland) for 30 min at 37° C. Afterwards, 0.5 lg mL 1 CLEC10A-Fc, CLEC10A H259T-Fc, DC-SIGN-Fc (all produced in house), or biotinylated Helix pomatia agglutinin (HPA; Sigma-Aldrich) or 1 lg mL 1 biotinylated soybean agglutinin (SBA; Vector Laboratories, Newark, CA, USA) were added for 1 h at room temperature (RT). .. Where indicated, lectins were pre-incubated with 10 mM EGTA (Thermo Fisher) for 15 min. Plates were washed and lectin binding was detected with a secondary horseradish peroxidase (HRP)-coupled goat-anti-human IgG Fc antibody (Jackson ImmunoResearch, West Grove, PA, USA) or streptavidin-HRP (MyBioSource, San Diego, CA, USA) for 30 min at RT.

    Produced:

    Article Title: Ligand-specific tuning of CLEC10A signalling strength and dendritic cell responses through engagement of different GalNAc-containing glycan structures.
    Article Snippet: See the T erm s and C onditions (https://onlinelibrary.w iley.com /term s-and-conditions) on W iley O nline L ibrary for rules of use; O A articles are governed by the applicable C reative C om m ons L icense acetic acid (Fluka, Charlotte, NC, USA/Sigma-Aldrich) in DMSO and incubated for 2 h at 37° C. Subsequently, glycodendrimers were separated from unbound oligosaccharides on PD10 desalting columns (Sigma-Aldrich) according to the manufacturer’s protocol and lyophilised at least five times to improve purity. .. To determine the lectin binding, glycodendrimers were serially diluted in 0.2 M NaHCO3 (Sigma-Aldrich; pH 9.2) and coated onto NUNC Maxisorp plates (Thermo Fisher, Waltham, MA, USA) overnight at 4° C. Plates were blocked with TSM (20 mM Tris, 150 mM NaCl, 2 mM MgCl2 (all Sigma-Aldrich) and 1 mM CaCl2 (VWR chemicals, Radnor, PA, USA)), containing 0.5% bovine serum albumin (BSA fraction V, Roche, Basel, Switzerland) for 30 min at 37° C. Afterwards, 0.5 lg mL 1 CLEC10A-Fc, CLEC10A H259T-Fc, DC-SIGN-Fc (all produced in house), or biotinylated Helix pomatia agglutinin (HPA; Sigma-Aldrich) or 1 lg mL 1 biotinylated soybean agglutinin (SBA; Vector Laboratories, Newark, CA, USA) were added for 1 h at room temperature (RT). .. Where indicated, lectins were pre-incubated with 10 mM EGTA (Thermo Fisher) for 15 min. Plates were washed and lectin binding was detected with a secondary horseradish peroxidase (HRP)-coupled goat-anti-human IgG Fc antibody (Jackson ImmunoResearch, West Grove, PA, USA) or streptavidin-HRP (MyBioSource, San Diego, CA, USA) for 30 min at RT.

    Whole Genome Amplification:

    Article Title: Glycopolymer-Functionalized Gold Nanoparticles for the Detection of Western Diamondback Rattlesnake ( Crotalus atrox ) Venom
    Article Snippet: High-performance liquid chromatography (HPLC)-grade acetonitrile (≥99.8%), glucose (lab-reagent grade), hexane fraction from petrol (lab-reagent grade), DCM (99% lab reagent grade), sodium hydrogen carbonate (≥99%), ethyl acetate (≥99.7%, analytical reagent grade), sodium chloride (≥99.5%), calcium chloride, 40–60 petroleum ether (lab reagent grade), hydrochloric acid (∼37%, analytical grade), glacial acetic acid (analytical grade), and magnesium sulfate (reagent grade) were purchased from Thermo Fisher Scientific. .. Soybean agglutinin (SBA) and wheat germ agglutinin (WGA) were purchased from Vector Laboratories. .. Naja naja (Indian cobra) venom was purchased from Latoxan.

    Article Title: Glycopolymer-Functionalized Gold Nanoparticles for the Detection of Western Diamondback Rattlesnake ( Crotalus atrox ) Venom.
    Article Snippet: High-performance liquid chromatography (HPLC)-grade acetonitrile (≥99.8%), glucose (lab-reagent grade), hexane fraction from petrol (lab-reagent grade), DCM (99% lab reagent grade), sodium hydrogen carbonate (≥99%), ethyl acetate (≥99.7%, analytical reagent grade), sodium chloride (≥99.5%), calcium chloride, 40−60 petroleum ether (lab reagent grade), hydrochloric acid (∼37%, analytical grade), glacial acetic acid (analytical grade), and magnesium sulfate (reagent grade) were purchased from Thermo Fisher Scientific. .. Soybean agglutinin (SBA) and wheat germ agglutinin (WGA) were purchased from Vector Laboratories. ..

    Article Title: Lipopolysaccharide Detection with Glycan-Specific Lectins—a Nonspecific Binding Approach Applied to Surface Plasmon Resonance
    Article Snippet: Phosphate buffer solution pH 7.4 (1X PBS) was purchased from Corning (Corning, US). .. Biotinylated lectins Concanavalin (ConA), Glycine max agglutinin (SBA), Triticum vulgaris agglutinin (WGA), Dolichos biflorus agglutinin (DBA), Ulex europaeus agglutinin (UEA I), Ricinus communis agglutinin (RCA), and Arachis hypogea agglutinin (PNA) were purchased from Vector Laboratories (Newark, US). .. Phenol extracted LPS from E. coli O55:B5 (CDC 1644-70), E. coli O111:B4 (private source), K. pneumoniae (ATCC 15830), P. aeruginosa (ATCC 27316), and S. enterica (ATCC 7823) were purchased from Sigma-Aldrich (Oakville, Canada).

    Enzyme-linked Immunosorbent Assay:

    Article Title: Aberrant glycosylation patterns as potential biomarkers for diagnosis and disease progression in bullous pemphigoid
    Article Snippet: .. Briefly, during Lectin ELISA of serum and blister fluid, biotinylated lectins were diluted with 1% BSA to the following concentrations: HPA-L (Vector, B-1115) 5μg/mL, SNA (Vector, B-1305) 0.5μg/mL, PSA (Vector, B-1055) 0.5μg/mL, SBA (Vector, B-1015) 0.5μg/mL, RCA120 (Vector, B-1085) 0.05μg/mL, AAL (Vector, B-1395) 0.01μg/mL, while during Lectin ELISA of saliva, biotinylated lectins were diluted to the following concentrations: HPA-L 5μg/mL, SNA 2μg/mL, PSA 1μg/mL, SBA 5μg/mL, RCA120 1μg/mL, AAL 1μg/mL. .. Streptavidin linked to HRP (Vector, SA-5014) was diluted 1:2000 and incubated at 37°C for 30 minutes.

    Concentration Assay:

    Article Title: Graph attention network-driven single-cell omics analysis reveals how B4GALNT1-mediated glycosylation remodelling of the ferroptosis-pyroptosis network promotes drug resistance in hepatocellular carcinoma.
    Article Snippet: .. BIE et al. 9 of 28 Biotin-labelled lectins, including Biotin-VVA (Vector Laboratories, B-1231, USA), Biotin-SBA (Vector Laboratories, B-1015, USA), and Biotin-PNA (Vector Laboratories, B1075, USA), were added at a working concentration of 1–3 μg/mL and incubated for 1.5 h at room temperature ..

    Incubation:

    Article Title: Graph attention network-driven single-cell omics analysis reveals how B4GALNT1-mediated glycosylation remodelling of the ferroptosis-pyroptosis network promotes drug resistance in hepatocellular carcinoma.
    Article Snippet: .. BIE et al. 9 of 28 Biotin-labelled lectins, including Biotin-VVA (Vector Laboratories, B-1231, USA), Biotin-SBA (Vector Laboratories, B-1015, USA), and Biotin-PNA (Vector Laboratories, B1075, USA), were added at a working concentration of 1–3 μg/mL and incubated for 1.5 h at room temperature ..



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    Correlation analysis of serum and blister fluid glycosylation with BP clinical indicators, and diagnostic accuracy assessed by ROC analysis. (a) Evaluation of the correlation between 6 glycosylation structures (binding to <t>PHA-L,</t> <t>SNA,</t> PSA, <t>SBA,</t> RCA120, AAL) and clinical indicators (BP180 and BP230 antibody titers, eosinophil count and percentage, white blood cell count, total serum IgE titer, erythrocyte sedimentation rate, high-sensitivity C-reactive protein level, hospital stay duration, age) in serum. (b) Evaluation of the correlation between 6 glycosylation structures (binding to PHA-L, SNA, PSA, SBA, RCA120, AAL) and clinical indicators (BP180 and BP230 antibody titers, eosinophil count and percentage, total protein, albumin, sodium, potassium, calcium ion concentrations, age, and the six glycosylation modifications) in blister fluid. Spearman’s correlation analysis was used for statistical testing. X indicates p>0.05 after statistical testing. Red color represents positive correlation, while blue color represents negative correlation. The larger and deeper the circle, the stronger the correlation coefficient. (c) ROC analysis for serum glycopatterns recognized by lectin PSA, SNA, SBA to discriminate BP patients from healthy controls. (d) ROC analysis for blister fluid glycopatterns recognized by lectin RCA120, SBA, AAL to discriminate BP patients from control group. The area under the curve (AUC) is used as a metric of diagnostic ability.
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    Lectin detection profiles. A total of 12 plasmon shift values, measured after 15 min of immobilization, were recorded for each lectin, with the average and standard deviation values represented by each band in the graph. Each lectin is used to create the LPS profiles for each bacterial species injected at 100 μg/mL, as well as a PBS buffer blank reference. The lectins chosen are Concanavalin (ConA), Glycine max <t>agglutinin</t> <t>(SBA),</t> Triticum vulgaris agglutinin (WGA), Dolichos biflorus agglutinin (DBA), Ulex europaeus agglutinin (UEA I), Ricinus communis agglutinin (RCA), and Arachis hypogea agglutinin (PNA). These lectins will be referred by their abbreviation for the next figures to avoid unnecessary length in the legend.
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    Lectin detection profiles. A total of 12 plasmon shift values, measured after 15 min of immobilization, were recorded for each lectin, with the average and standard deviation values represented by each band in the graph. Each lectin is used to create the LPS profiles for each bacterial species injected at 100 μg/mL, as well as a PBS buffer blank reference. The lectins chosen are Concanavalin (ConA), Glycine max <t>agglutinin</t> <t>(SBA),</t> Triticum vulgaris agglutinin (WGA), Dolichos biflorus agglutinin (DBA), Ulex europaeus agglutinin (UEA I), Ricinus communis agglutinin (RCA), and Arachis hypogea agglutinin (PNA). These lectins will be referred by their abbreviation for the next figures to avoid unnecessary length in the legend.
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    Correlation analysis of serum and blister fluid glycosylation with BP clinical indicators, and diagnostic accuracy assessed by ROC analysis. (a) Evaluation of the correlation between 6 glycosylation structures (binding to PHA-L, SNA, PSA, SBA, RCA120, AAL) and clinical indicators (BP180 and BP230 antibody titers, eosinophil count and percentage, white blood cell count, total serum IgE titer, erythrocyte sedimentation rate, high-sensitivity C-reactive protein level, hospital stay duration, age) in serum. (b) Evaluation of the correlation between 6 glycosylation structures (binding to PHA-L, SNA, PSA, SBA, RCA120, AAL) and clinical indicators (BP180 and BP230 antibody titers, eosinophil count and percentage, total protein, albumin, sodium, potassium, calcium ion concentrations, age, and the six glycosylation modifications) in blister fluid. Spearman’s correlation analysis was used for statistical testing. X indicates p>0.05 after statistical testing. Red color represents positive correlation, while blue color represents negative correlation. The larger and deeper the circle, the stronger the correlation coefficient. (c) ROC analysis for serum glycopatterns recognized by lectin PSA, SNA, SBA to discriminate BP patients from healthy controls. (d) ROC analysis for blister fluid glycopatterns recognized by lectin RCA120, SBA, AAL to discriminate BP patients from control group. The area under the curve (AUC) is used as a metric of diagnostic ability.

    Journal: Frontiers in Immunology

    Article Title: Aberrant glycosylation patterns as potential biomarkers for diagnosis and disease progression in bullous pemphigoid

    doi: 10.3389/fimmu.2025.1538126

    Figure Lengend Snippet: Correlation analysis of serum and blister fluid glycosylation with BP clinical indicators, and diagnostic accuracy assessed by ROC analysis. (a) Evaluation of the correlation between 6 glycosylation structures (binding to PHA-L, SNA, PSA, SBA, RCA120, AAL) and clinical indicators (BP180 and BP230 antibody titers, eosinophil count and percentage, white blood cell count, total serum IgE titer, erythrocyte sedimentation rate, high-sensitivity C-reactive protein level, hospital stay duration, age) in serum. (b) Evaluation of the correlation between 6 glycosylation structures (binding to PHA-L, SNA, PSA, SBA, RCA120, AAL) and clinical indicators (BP180 and BP230 antibody titers, eosinophil count and percentage, total protein, albumin, sodium, potassium, calcium ion concentrations, age, and the six glycosylation modifications) in blister fluid. Spearman’s correlation analysis was used for statistical testing. X indicates p>0.05 after statistical testing. Red color represents positive correlation, while blue color represents negative correlation. The larger and deeper the circle, the stronger the correlation coefficient. (c) ROC analysis for serum glycopatterns recognized by lectin PSA, SNA, SBA to discriminate BP patients from healthy controls. (d) ROC analysis for blister fluid glycopatterns recognized by lectin RCA120, SBA, AAL to discriminate BP patients from control group. The area under the curve (AUC) is used as a metric of diagnostic ability.

    Article Snippet: Briefly, during Lectin ELISA of serum and blister fluid, biotinylated lectins were diluted with 1% BSA to the following concentrations: HPA-L (Vector, B-1115) 5μg/mL, SNA (Vector, B-1305) 0.5μg/mL, PSA (Vector, B-1055) 0.5μg/mL, SBA (Vector, B-1015) 0.5μg/mL, RCA120 (Vector, B-1085) 0.05μg/mL, AAL (Vector, B-1395) 0.01μg/mL, while during Lectin ELISA of saliva, biotinylated lectins were diluted to the following concentrations: HPA-L 5μg/mL, SNA 2μg/mL, PSA 1μg/mL, SBA 5μg/mL, RCA120 1μg/mL, AAL 1μg/mL.

    Techniques: Glycoproteomics, Diagnostic Assay, Binding Assay, Cell Counting, Sedimentation, Control

    Alterations of glycopatterns in saliva of BP patients. (a) Comparative analysis of relative expression levels of 37 lectin-specific glycan structures in saliva samples of BP patients compared to healthy controls. The ratio of the BP group to the control group was logarithmically converted to a base of 1.5. A ratio >1 indicates an increase of more than 1.5 times compared to the control group, whereas a ratio <-1 denotes a decrease of over 0.67 times compared to the control group. High expression is depicted in red, while low expression is represented in blue. (b) Heat map of lectin with significant differentiation between BP patients and healthy controls. (c) The lectin ELISA confirmed that 3 glycans (binding to SNA, SBA, AAL) were significantly increased in the saliva of BP patients (n=20) compared to healthy controls (n=20). The data are presented as Mean ± SD. Analysis was performed using Wilcoxon Mann-Whitney test. (d) The ELISA was conducted to determine the positive rate of anti-BP180-NC16A antibodies in the saliva of BP patients. (e) Relationship between the presence of anti-BP180-NC16A antibodies in saliva and mucosal damage in BP patients. The data were presented as proportions, and statistical analysis was performed using chi-square test. (f) Differential analysis comparing the glycosylation structures (SNA) confirmed by lectin ELISA in the BP180 antibody-positive (n=12) and -negative groups (n=8) in saliva. The Wilcoxon Mann-Whitney test was used for statistical analysis.

    Journal: Frontiers in Immunology

    Article Title: Aberrant glycosylation patterns as potential biomarkers for diagnosis and disease progression in bullous pemphigoid

    doi: 10.3389/fimmu.2025.1538126

    Figure Lengend Snippet: Alterations of glycopatterns in saliva of BP patients. (a) Comparative analysis of relative expression levels of 37 lectin-specific glycan structures in saliva samples of BP patients compared to healthy controls. The ratio of the BP group to the control group was logarithmically converted to a base of 1.5. A ratio >1 indicates an increase of more than 1.5 times compared to the control group, whereas a ratio <-1 denotes a decrease of over 0.67 times compared to the control group. High expression is depicted in red, while low expression is represented in blue. (b) Heat map of lectin with significant differentiation between BP patients and healthy controls. (c) The lectin ELISA confirmed that 3 glycans (binding to SNA, SBA, AAL) were significantly increased in the saliva of BP patients (n=20) compared to healthy controls (n=20). The data are presented as Mean ± SD. Analysis was performed using Wilcoxon Mann-Whitney test. (d) The ELISA was conducted to determine the positive rate of anti-BP180-NC16A antibodies in the saliva of BP patients. (e) Relationship between the presence of anti-BP180-NC16A antibodies in saliva and mucosal damage in BP patients. The data were presented as proportions, and statistical analysis was performed using chi-square test. (f) Differential analysis comparing the glycosylation structures (SNA) confirmed by lectin ELISA in the BP180 antibody-positive (n=12) and -negative groups (n=8) in saliva. The Wilcoxon Mann-Whitney test was used for statistical analysis.

    Article Snippet: Briefly, during Lectin ELISA of serum and blister fluid, biotinylated lectins were diluted with 1% BSA to the following concentrations: HPA-L (Vector, B-1115) 5μg/mL, SNA (Vector, B-1305) 0.5μg/mL, PSA (Vector, B-1055) 0.5μg/mL, SBA (Vector, B-1015) 0.5μg/mL, RCA120 (Vector, B-1085) 0.05μg/mL, AAL (Vector, B-1395) 0.01μg/mL, while during Lectin ELISA of saliva, biotinylated lectins were diluted to the following concentrations: HPA-L 5μg/mL, SNA 2μg/mL, PSA 1μg/mL, SBA 5μg/mL, RCA120 1μg/mL, AAL 1μg/mL.

    Techniques: Expressing, Glycoproteomics, Control, Enzyme-linked Immunosorbent Assay, Binding Assay, MANN-WHITNEY

    Correlation of salivary glycosylation with BP clinical indicators and diagnostic accuracy of selected lectins via ROC analysis. (a) Correlation analysis was conducted to identify the relationship between changes in six glycan structures (specifically binding to PHA-L, SNA, PSA, SBA, RCA120, and AAL) in saliva and disease severity indicators (BP180 antibody titer, BP230 antibody titer, erythema and wheal score, mucosal damage score, BPDAI score). BP patients were categorized into four subgroups based on the positivity of salivary anti-BP180-NC16A and the presence of oral mucosal damage. Spearman’s correlation analysis was used for statistical testing. X indicates p>0.05 after statistical testing. Red color represents positive correlation, while blue color represents negative correlation. The larger and deeper the circle, the stronger the correlation coefficient. The numerical values in the middle represent the Spearman correlation coefficients. (b) Changes in the glycan structures bound to SNA, and AAL in the saliva of BP patients were detected using lectin ELISA before treatment at admission and after significant improvement at discharge (n=11). The Wilcoxon Signed-Rank test was used for statistical analysis. (c) ROC analysis was conducted to assess the glycan structures bound to SNA and AAL in saliva as biomarkers. AUC was used as an indicator to evaluate diagnostic capability.

    Journal: Frontiers in Immunology

    Article Title: Aberrant glycosylation patterns as potential biomarkers for diagnosis and disease progression in bullous pemphigoid

    doi: 10.3389/fimmu.2025.1538126

    Figure Lengend Snippet: Correlation of salivary glycosylation with BP clinical indicators and diagnostic accuracy of selected lectins via ROC analysis. (a) Correlation analysis was conducted to identify the relationship between changes in six glycan structures (specifically binding to PHA-L, SNA, PSA, SBA, RCA120, and AAL) in saliva and disease severity indicators (BP180 antibody titer, BP230 antibody titer, erythema and wheal score, mucosal damage score, BPDAI score). BP patients were categorized into four subgroups based on the positivity of salivary anti-BP180-NC16A and the presence of oral mucosal damage. Spearman’s correlation analysis was used for statistical testing. X indicates p>0.05 after statistical testing. Red color represents positive correlation, while blue color represents negative correlation. The larger and deeper the circle, the stronger the correlation coefficient. The numerical values in the middle represent the Spearman correlation coefficients. (b) Changes in the glycan structures bound to SNA, and AAL in the saliva of BP patients were detected using lectin ELISA before treatment at admission and after significant improvement at discharge (n=11). The Wilcoxon Signed-Rank test was used for statistical analysis. (c) ROC analysis was conducted to assess the glycan structures bound to SNA and AAL in saliva as biomarkers. AUC was used as an indicator to evaluate diagnostic capability.

    Article Snippet: Briefly, during Lectin ELISA of serum and blister fluid, biotinylated lectins were diluted with 1% BSA to the following concentrations: HPA-L (Vector, B-1115) 5μg/mL, SNA (Vector, B-1305) 0.5μg/mL, PSA (Vector, B-1055) 0.5μg/mL, SBA (Vector, B-1015) 0.5μg/mL, RCA120 (Vector, B-1085) 0.05μg/mL, AAL (Vector, B-1395) 0.01μg/mL, while during Lectin ELISA of saliva, biotinylated lectins were diluted to the following concentrations: HPA-L 5μg/mL, SNA 2μg/mL, PSA 1μg/mL, SBA 5μg/mL, RCA120 1μg/mL, AAL 1μg/mL.

    Techniques: Glycoproteomics, Diagnostic Assay, Binding Assay, Enzyme-linked Immunosorbent Assay

    Lectin detection profiles. A total of 12 plasmon shift values, measured after 15 min of immobilization, were recorded for each lectin, with the average and standard deviation values represented by each band in the graph. Each lectin is used to create the LPS profiles for each bacterial species injected at 100 μg/mL, as well as a PBS buffer blank reference. The lectins chosen are Concanavalin (ConA), Glycine max agglutinin (SBA), Triticum vulgaris agglutinin (WGA), Dolichos biflorus agglutinin (DBA), Ulex europaeus agglutinin (UEA I), Ricinus communis agglutinin (RCA), and Arachis hypogea agglutinin (PNA). These lectins will be referred by their abbreviation for the next figures to avoid unnecessary length in the legend.

    Journal: ACS Omega

    Article Title: Lipopolysaccharide Detection with Glycan-Specific Lectins—a Nonspecific Binding Approach Applied to Surface Plasmon Resonance

    doi: 10.1021/acsomega.5c00867

    Figure Lengend Snippet: Lectin detection profiles. A total of 12 plasmon shift values, measured after 15 min of immobilization, were recorded for each lectin, with the average and standard deviation values represented by each band in the graph. Each lectin is used to create the LPS profiles for each bacterial species injected at 100 μg/mL, as well as a PBS buffer blank reference. The lectins chosen are Concanavalin (ConA), Glycine max agglutinin (SBA), Triticum vulgaris agglutinin (WGA), Dolichos biflorus agglutinin (DBA), Ulex europaeus agglutinin (UEA I), Ricinus communis agglutinin (RCA), and Arachis hypogea agglutinin (PNA). These lectins will be referred by their abbreviation for the next figures to avoid unnecessary length in the legend.

    Article Snippet: Biotinylated lectins Concanavalin (ConA), Glycine max agglutinin (SBA), Triticum vulgaris agglutinin (WGA), Dolichos biflorus agglutinin (DBA), Ulex europaeus agglutinin (UEA I), Ricinus communis agglutinin (RCA), and Arachis hypogea agglutinin (PNA) were purchased from Vector Laboratories (Newark, US).

    Techniques: Standard Deviation, Injection