BlotGlyco® Glycan Purification and Labeling Kit

$450.00$7,200.00

BlotGlyco® Beads: Polymer beads are densely covered with hydrazide groups to facilitate glycan capture

  • BlotGlyco® is a sample preparation kit for glycan analysis of biological samples.
  • Using this kit will purify and label glycans from the crude samples such as glycoprotein, serum, cell, organ, plant tissue and so on. The label is selectable depending on detection methods including HPLC, LC-MS, MALDI-TOF MS and so on.
  • BlotGlyco® beads are coated with dense hydrazide functional groups, which enable specific binding with aldehyde groups at the reducing end of glycan. The hydrazide groups on the beads form stable covalent bond with aldehyde; therefore, it allows the vigorous washing steps to eliminate peptide and other impurities.
  • BlotGlyco® kit is a useful tool for isolating glycans from the variety of biological samples, selectively and comprehensively.

 

Product Description

BlotGlyco® Beads: Polymer beads are densely covered with hydrazide groups to facilitate glycan capture

  • BlotGlyco® is a sample preparation kit for glycan analysis of biological samples.
  • Using this kit will purify and label glycans from the crude samples such as glycoprotein, serum, cell, organ, plant tissue and so on. The label is selectable depending on detection methods including HPLC, LC-MS, MALDI-TOF MS and so on.
  • BlotGlyco® beads are coated with dense hydrazide functional groups, which enable specific binding with aldehyde groups at the reducing end of glycan. The hydrazide groups on the beads form stable covalent bond with aldehyde; therefore, it allows the vigorous washing steps to eliminate peptide and other impurities.
  • BlotGlyco® kit is a quite useful tool for isolating glycans from the variety of biological samples, selectively and comprehensively.

Application

Sample Preparation for Glycan Analysis

GlycoBeads for Glycan chart.png

Our sample preperation for glycan analysis is a streamlined process, optimized for screening N-glycan in large sample batches during cell line selection, upstream and downstream process development.

A streamlined process, optimized for screening N-glycans in large sample batches during cell line selection, upstream and downstream process development.

  • Glycosylation analysis of biologics (for research, screening, quality control and production process monitoring)
  • Glycosylation analysis of cells, especially for the differentiation researches of stem cells
  • Combination of glycomics and proteomics (glycans can be analyzed from electrohoresis bands)
  • Glycan biomarker discovery
  • Free oligosaccharide purification and analysis in human milk and urine

Features

  • Purification and labeling are completed in about 5 hours using just one spin tube
  • No special equipment is necessary except a heating block and a small desktop centrifuge. No column chromatography is necessary.
  • Glycans can be purified and labeled from various crude biological samples. Conventional fluorescent labeling reagents (2AB, PA) are applicable. Kit contains a unique labeling reagent for the high sensitive MALDI-TOF MS measurement.
  • By using a 96 well filter plate and a vacuum manifold, as many as 96 samples are processed simultaneously.

Automating Glycan Sample Prep

BlotGlyco-Glycan Purification and Labeling Kit

Experiments

Biomarker discovery

  • N-glycan of human serum: using 5μL serum
    blotglyco-exp-biomarker

Glycosylation analysis of Biologics

  • N-glycan of antibody: using 10μg IgG
    blotglyco-exp-biologics

  1. INAFUKU, Saori, et al. A comparison of N-glycan profiles in human plasma and vitreous fluid. Graefe’s Archive for Clinical and Experimental Ophthalmology, 2014, 252.8: 1235-1243.
  2. ONITSUKA, Masayoshi, et al. Glycosylation analysis of an aggregated antibody produced by Chinese hamster ovary cells in bioreactor culture. Journal of bioscience and bioengineering, 2014, 117.5: 639-644.
  3. ISHIBASHI, Yusuke, et al. Serum tri‐and tetra‐antennary N‐glycan is a potential predictive biomarker for castration‐resistant prostate cancer. The Prostate, 2014, 74.15: 1521-1529.
  4. YAMASAKI, Yasushi, et al. Use of noninvasive serum glycan markers to distinguish nonalcoholic steatohepatitis from simple steatosis. Journal of gastroenterology and hepatology, 2014.
  5. HATAKEYAMA, Shingo, et al. Serum< i> N-Glycan Alteration Associated with Renal Cell Carcinoma Detected by High Throughput Glycan Analysis. The Journal of urology, 2014, 191.3: 805-813.
  6. SUDO, Makoto, et al. Different IVIG Glycoforms Affect In Vitro Inhibition of Anti-Ganglioside Antibody-Mediated Complement Deposition. PloS one, 2014, 9.9: e107772.
  7. SHINOHARA, Yasuro; FURUKAWA, Jun-ichi. Surface Plasmon Resonance as a Tool to Characterize Lectin–Carbohydrate Interactions. In: Lectins. Springer New York, 2014. p. 185-205.
  8. ISHIHARA, Takeshi, et al. Discovery of novel differentiation markers in the early stage of chondrogenesis by glycoform-focused reverse proteomics and genomics. Biochimica et Biophysica Acta (BBA)-General Subjects, 2014, 1840.1: 645-655.
  9. MITSUDOME, Takumi, et al. Expression, Purification, and Characterization of Endo-β-N-Acetylglucosaminidase H Using Baculovirus-Mediated Silkworm Protein Expression System. Applied biochemistry and biotechnology, 2014, 172.8: 3978-3988.
  10. NOMURA, Tsuyoshi, et al. Improvement of glycosylation structure by suppression of β-< i> N-acetylglucosaminidases in silkworm. Journal of bioscience and bioengineering, 2014.
  11. ITO, Kiyoaki, et al. Lack of Galactosylation Enhances the Pathogenic Activity of IgG1 but Not IgG2a Anti-Erythrocyte Autoantibodies. The Journal of Immunology, 2014, 192.2: 581-588.
  12. YUYAMA, Kohei, et al. Decreased Amyloid-β Pathologies by Intracerebral Loading of Glycosphingolipid-enriched Exosomes in Alzheimer Model Mice. Journal of Biological Chemistry, 2014, 289.35: 24488-24498.
  13. KITAZAWA, Kiminari, et al. β-Galactosyl Yariv reagent binds to the β-1, 3-galactan of arabinogalactan proteins. Plant physiology, 2013, 161.3: 1117-1126.
  14. ASAO, Takayuki, et al. Development of a Novel System for Mass Spectrometric Analysis of Cancer-Associated Fucosylation in Plasma α 1-Acid Glycoprotein. BioMed research international, 2013, 2013.
  15. KANEKO, Kentaro, et al. Rapid and High-Throughput N-Glycomic Analysis of Plant Glycoproteins. In: Plant Proteomics. Humana Press, 2014. p. 645-653.
  16. HATAKEYAMA, Shingo, et al. Serum N-Glycan Profiling Predicts Prognosis in Patients Undergoing Hemodialysis. The Scientific World Journal, 2013, 2013.
  17. DONG, Weijie; MATSUNO, Yu‐ki; KAMEYAMA, Akihiko. Serum protein fractionation using supported molecular matrix electrophoresis. Electrophoresis, 2013, 34.16: 2432-2439.
  18. NOUSO, Kazuhiro, et al. Clinical utility of high-throughput glycome analysis in patients with pancreatic cancer. Journal of gastroenterology, 2013, 48.10: 1171-1179.
  19. KATO, Kentaro, et al. Sialic acid-dependent attachment of mucins from three mouse strains to< i> Entamoeba histolytica. Biochemical and biophysical research communications, 2013, 436.2: 252-258.
  20. HUANG, Sheng-He, et al. Chemoinfectomics in Drug Design and Development. Anti-Infective Agents, 2013, 11.2: 100-108.
  21. KAMIYAMA, Toshiya, et al. Identification of novel serum biomarkers of hepatocellular carcinoma using glycomic analysis. Hepatology, 2013, 57.6: 2314-2325.
  22. MIYAHARA, Koji, et al. Serum glycan markers for evaluation of disease activity and prediction of clinical course in patients with ulcerative colitis. PloS one, 2013, 8.10: e74861.
  23. FURUKAWA, Jun-ichi; FUJITANI, Naoki; SHINOHARA, Yasuro. Recent advances in cellular glycomic analyses. Biomolecules, 2013, 3.1: 198-225.
  24. NAGATA, Yudai, et al. RNAi suppression of β-N-acetylglucosaminidase (BmFDL) for complex-type N-linked glycan synthesis in cultured silkworm cells. Biotechnology letters, 2013, 35.7: 1009-1016.
  25. TAKEUCHI, Motoi, et al. N-and O-glycome analysis of serum and urine from bladder cancer patients using a high-throughput glycoblotting method. Journal of Glycomics & Lipidomics, 2013.
  26. KWASE, Yoshiyuki A.; COCHRAN, Melissa; NITZ, Mark. Protecting‐Group‐Free Glycoconjugate Synthesis: Hydrazide and Oxyamine Derivatives in N‐Glycoside Formation. Modern Synthetic Methods in Carbohydrate Chemistry: From Monosaccharides to Complex Glycoconjugates, 2013, 67-96.
  27. URASHIMA, Tadasu, et al. Recent advances in studies on milk oligosaccharides of cows and other domestic farm animals. Bioscience, biotechnology, and biochemistry, 2013, 77.3: 455-466.
  28. YAMADA, Keita; HIRABAYASHI, Jun; KAKEHI, Kazuaki. Analysis of O-glycans as 9-fluorenylmethyl derivatives and its application to the studies on glycan array. Analytical chemistry, 2013, 85.6: 3325-3333.
  29. MATSUSHITA, Takahiko, et al. Site-specific conformational alteration induced by sialylation of MUC1 tandem repeating glycopeptides at an epitope region for the anti-KL-6 monoclonal antibody. Biochemistry, 2013, 52.2: 402-414.
  30. FURUKAWA, Takayuki, et al. Glycoblotting-based high throughput protocol for the structural characterization of hyaluronan degradation products during enzymatic fragmentation. Glycoconjugate journal, 2013, 30.2: 171-182.
  31. NAGAHORI, Noriko, et al. Effect of Ganglioside GM3 Synthase Gene Knockout on the Glycoprotein N‐Glycan Profile of Mouse Embryonic Fibroblast. ChemBioChem, 2013, 14.1: 73-82.
  32. KUMAR HV, Ravi, et al. A New Approach for the Synthesis of Hyperbranched N-Glycan Core Structures from Locust Bean Gum. Organic letters, 2013, 15.24: 6278-6281.
  33. FUJITANI, Naoki, et al. Total cellular glycomics allows characterizing cells and streamlining the discovery process for cellular biomarkers. Proceedings of the National Academy of Sciences, 2013, 110.6: 2105-2110.
  34. SHINOHARA, Yasuro; FUJITANI, Naoki; FURUKAWA, Jun-ichi. Total Cellular Glycomics: A Glycomic Approach to Describe Cells and Streamline the Discovery Process for Cellular Biomarkers. TRENDS IN GLYCOSCIENCE AND GLYCOTECHNOLOGY, 2013, 25.141: 103-116.
  35. YAMADA, Kazunori, et al. Galactosylation of IgG1 modulates FcγRIIB-mediated inhibition of murine autoimmune hemolytic anemia. Journal of autoimmunity, 2013, 47: 104-110.
  36. KOUGUCHI, Hirokazu, et al. Characterization of a Surface Glycoprotein from Echinococcus multilocularis and Its Mucosal Vaccine Potential in Dogs. PloS one, 2013, 8.7: e69821.
  37. KATO, Atsushi, et al. α-1-C-Butyl-1, 4-dideoxy-1, 4-imino-l-arabinitol as a Second-Generation Iminosugar-Based Oral α-Glucosidase Inhibitor for Improving Postprandial Hyperglycemia. Journal of medicinal chemistry, 2012, 55.23: 10347-10362.
  38. ABE, Midori, et al. A cross-linked polymer possessing a high density of hydrazide groups: high-throughput glycan purification and labeling for high-performance liquid chromatography analysis. Polymer journal, 2011, 44.3: 269-277.
  39. AMANO, Maho; HASHIMOTO, Ryo; NISHIMURA, Shin‐ Effects of Single Genetic Damage in Carbohydrate‐Recognizing Proteins in Mouse Serum N‐Glycan Profile Revealed by Simple Glycotyping Analysis. ChemBioChem, 2012, 13.3: 451-464.
  40. NAKAGAWA, Tsutomu, et al. Analysis of polarized secretion of fucosylated alpha-fetoprotein in HepG2 cells. Journal of proteome research, 2012, 11.5: 2798-2806.
  41. AMANO, Maho, et al. Tumour suppressor p16INK4a–anoikis‐favouring decrease in N/O‐glycan/cell surface sialylation by down‐regulation of enzymes in sialic acid biosynthesis in tandem in a pancreatic carcinoma model. FEBS Journal, 2012, 279.21: 4062-4080.
  42. ONITSUKA, Masayoshi, et al. Enhancement of sialylation on humanized IgG-like bispecific antibody by overexpression of α2, 6-sialyltransferase derived from Chinese hamster ovary cells. Applied microbiology and biotechnology, 2012, 94.1: 69-80.
  43. YANG, Shuang; ZHANG, Hui. Solid‐phase glycan isolation for glycomics analysis. PROTEOMICS-Clinical Applications, 2012, 6.11-12: 596-608.
  44. OTANI, Masako, et al. Sialylation determines the nephritogenicity of IgG3 cryoglobulins. Journal of the American Society of Nephrology, 2012, 23.11: 1869-1878.
  45. NISHIMURA, Shin‐Ichiro, et al. Glycomics for Drug Discovery: Metabolic Perturbation in Androgen‐Independent Prostate Cancer Cells Induced by Unnatural Hexosamine Mimics. Angewandte Chemie International Edition, 2012, 51.14: 3386-3390.
  46. SEITO, Naoki, et al. Interruption of glycosphingolipid synthesis enhances osteoarthritis development in mice. Arthritis & Rheumatism, 2012, 64.8: 2579-2588.
  47. TSUKUDA, Yukinori, et al. Ganglioside GM3 has an essential role in the pathogenesis and progression of rheumatoid arthritis. PloS one, 2012, 7.6: e40136.
  48. NISHIMURA, Shin-Ichiro. Toward automated glycan analysis. Advances in carbohydrate chemistry and biochemistry, 2011, 65: 220.
  49. TAKIMORI, Shota, et al. Alteration of the N‐glycome of bovine milk glycoproteins during early lactation. FEBS Journal, 2011, 278.19: 3769-3781.
  50. TAKEGAWA, Yasuhiro, et al. Simultaneous analysis of heparan sulfate, chondroitin/dermatan sulfates, and hyaluronan disaccharides by glycoblotting-assisted sample preparation followed by single-step zwitter-ionic-hydrophilic interaction chromatography. Analytical chemistry, 2011, 83.24: 9443-9449.
  51. FUJITANI, Naoki, et al. Qualitative and quantitative cellular glycomics of glycosphingolipids based on rhodococcal endoglycosylceramidase-assisted glycan cleavage, glycoblotting-assisted sample preparation, and matrix-assisted laser desorption ionization tandem time-of-flight mass spectrometry analysis. Journal of Biological Chemistry, 2011, 286.48: 41669-41679.
  52. FUKUDA, Tomohiko, et al. α1, 6-Fucosyltransferase-deficient Mice Exhibit Multiple Behavioral Abnormalities Associated with a Schizophrenia-like Phenotype IMPORTANCE OF THE BALANCE BETWEEN THE DOPAMINE AND SEROTONIN SYSTEMS. Journal of Biological Chemistry, 2011, 286.21: 18434-18443.
  53. TAKIMORI, Shota, et al. Alteration of the N‐glycome of bovine milk glycoproteins during early lactation. FEBS Journal, 2011, 278.19: 3769-3781.
  54. HIROSE, Kazuko, et al. Insight into glycan diversity and evolutionary lineage based on comparative Avio-N-glycomics and sialic acid analysis of 88 egg whites of galloanserae. Biochemistry, 2011, 50.21: 4757-4774.
  55. OHYANAGI, Tatsuya, et al. Importance of sialic acid residues illuminated by live animal imaging using phosphorylcholine self-assembled monolayer-coated quantum dots. Journal of the American Chemical Society, 2011, 133.32: 12507-12517.
  56. INAGAKI, Mizuho, et al. The multiplicity of n-glycan structures of bovine milk 18 kDa lactophorin (milk glyCAM-1). Bioscience, biotechnology, and biochemistry, 2010, 74.2: 447-450.
  57. MIURA, Yoshiaki, et al. Glycoblotting-assisted O-glycomics: ammonium carbamate allows for highly efficient O-glycan release from glycoproteins. Analytical chemistry, 2010, 82.24: 10021-10029.
  58. KIMURA, Aiko, et al. Carbohydrate moieties contribute significantly to the physicochemical properties of French bean 7S globulin phaseolin. Journal of agricultural and food chemistry, 2010, 58.5: 2923-2930.
  59. AMANO, Maho, et al. Threshold in stage-specific embryonic glycotypes uncovered by a full portrait of dynamic N-glycan expression during cell differentiation. Molecular & Cellular Proteomics, 2010, 9.3: 523-537.
  60. AMANO, Maho; NISHIMURA, Shin-Ichiro. Chapter Four-Large-Scale Glycomics for Discovering Cancer‐Associated< i> N-Glycans by Integrating Glycoblotting and Mass Spectrometry. Methods in enzymology, 2010, 478: 109-125.
  61. SATO, Masaki, et al. High-sensitivity analysis of naturally occurring sugar chains, using a novel fluorescent linker molecule. Journal of biochemistry, 2009, 146.1: 33-41.
  62. MATSUMOTO, Kazuko, et al. Identification of predictive biomarkers for response to trastuzumab using plasma FUCA activity and N-glycan identified by MALDI-TOF-MS. Journal of proteome research, 2009, 8.2: 457-462.
  63. UEMATSU, Rie, et al. Glycosylation specific for adhesion molecules in epidermis and its receptor revealed by glycoform-focused reverse genomics. Molecular & Cellular Proteomics, 2009, 8.2: 232-244.
  64. MIURA, Yoshiaki; NISHIMURA, Shin-Ichiro. BlotGlyco (R) and glycoblotting for large scale, high throughput glycomics. TRENDS IN GLYCOSCIENCE AND GLYCOTECHNOLOGY, 2008, 20.111: 17-27.
  65. MIURA, Yoshiaki, et al. BlotGlycoABC™, an integrated glycoblotting technique for rapid and large scale clinical glycomics. Molecular & cellular proteomics, 2008, 7.2: 370-377.
  66. FURUKAWA, Jun-ichi, et al. Comprehensive approach to structural and functional glycomics based on chemoselective glycoblotting and sequential tag conversion. Analytical chemistry, 2008, 80.4: 1094-1101.
  67. PERKEL, Jeffrey M. Research Profile: At last, large-scale functional glycomics. Analytical Chemistry, 2008, 80.5: 1354-1355.
  68. SHIMAOKA, Hideyuki, et al. One‐Pot Solid‐Phase Glycoblotting and Probing by Transoximization for High‐Throughput Glycomics and Glycoproteomics. Chemistry-A European Journal, 2007, 13.6: 1664-1673.

Available Options

Catalog No.ItemPolymer BeadsReaction TubeCleanup ColumnPriceQuantity
#BS-45407ZBlotGlyco 100B100 Assays100100$3,840.00
#BS-45408ZBlotGlyco 100C100 AssaysNo Reaction TubesNo Cleanup Columns$3,600.00
#BS-45409ZBlotGlyco 100D100 AssaysNo Reaction Tubes100$3,760.00
#BS-45410ZBlotGlyco 200C200 AssaysNo Reaction TubesNo Cleanup Columns$7,200.00
#BS-45411ZBlotGlyco 100E100 Assays100No Cleanup Columns$3,680.00
#BS-45412ZBlotGlyco 200E200 Assays200No Cleanup Columns$7,200.00
#BS-45413ZBlotGlyco 96 plate B96 Assays1 Filterplate1 Cleanup Plate$3,840.00
#BS-45414ZBlotGlyco 10B10 Assays1010$450.00
#BS-45415ZBlotGlyco 50B50 Assays5050$2,025.00

Title