Chitin Resin from New England Biolabs

Product Specs
ItemChitin Resin
CompanyNew England Biolabs
Price $129.00 Inquire
Catalog NumberS6651S
Capacity2.0 mg maltose-binding protein
Matrixaffinity matrix
Quantity20 ml
ApplicationsProteomics & Glycomics
Product TypeResins
ModeAffinity Purification
Temperature4 C

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New England Biolabs

240 County Road

Ipswich, Massachusetts 1938

United States

Phone: 800-632-5227
800-632-7799
978-921-1350

Company Profile

Website: http://www.neb.com

(1) Reprogramming of bacterial virulence by lysine acetylationNat CommunApril 27, 2026Ole Schmöker, Britta Girbardt, Sabrina Schulze, Gottfried J. Palm, Leona Berndt, Jens Hoppen, Nilüfer Kara, Xenia Schöps, Ruba Al-Abdulla, Klara Garz, et al.75 mM NaCl) on a chitin matrix gravity flow column (New England Biolabs, Frankfurt/Main DE, cat. no S6651L). After extensive washing with high salt washing buffer (20 mM HEPES, sodium acetate pH 6.5, 500 mM

(2) Chemically Defined Non-human Glycans Comprising Galactose-α1-3-Galactose (α-Gal) Epitopes Glycoengineered into the Fragment Antigen-Binding (Fab) Domain of Cetuximab Differentially Affect Human Anti-α-Gal Immunoglobulin E (IgE) BindingACS Pharmacology & Translational ScienceApril 10, 2026Grayson Hatfield, Lioudmila Tepliakova, Roger Y. TamDIN#02271249) was purchased from McKesson Canada. Chitin resin (50 μL slurry, New England Biolabs, catalog no. S6651S) was washed twice with 50 mM Tris buffer (pH 7.3), and EndoS-CBD (1.0 μL, New England Biolabs, catalog

(3) CUT&Tag for High-Resolution Epigenomic Profiling From a Low Amount of Arabidopsis TissuePlant DirectApril 10, 2026Yixuan Fu, Marc W. Schmid, Sara Simoninithen centrifuged at 31,000 × g, 4°C, for 30 min and the supernatant mixed with 5 mL Chitin Resin (NEB #S6651), previously washed first with 30 mL of ddH2O and then 20 mL of HEGX buffer. The samples were incubated

(4) A Nanobody-Based Toolbox to Probe ApoE4 in the Secretory Pathway and CytosolCellsMarch 6, 2026Laure Vandevelde, Olivier Zwaenepoel, Edith De Bruycker, Maurits Ranson, Clara Van Stichel, Charlien Matthys, Jan Gettemansintein tag fusion protein was applied to chitin beads (New England BioLabs, Ipswich, MA, USA, cat. no. S6651S) according to the manufacturer’s instructions for IMPACT purification. Purity was assessed via SDS-PAGE

(5) Human iPSC-based Modeling of Pulmonary Fibrosis Reveals p300/CBP Inhibition Suppresses Alveolar Transitional Cell StateNat CommunFebruary 12, 2026Yusuke Tsutsui, Atsushi Masui, Satoshi Konishi, Taro Tsujimura, Mio Iwasaki, Takuya Yamamoto, Shimpei Gotoh(Addgene, 124601, a gift from Prof. Steven Henikoff) using a column filled with chitin beads (NEB, S6651L) after solubilization with sonication using Bioruptor II TYPE24 (Sonicbio, BR2024A). The transposase

(6) Heterochromatome wide analyses reveal MBD2 as a phase separation scaffold for heterochromatin compartmentalization and compositionNucleic Acids ResDecember 11, 2025Hui Zhang, Enes Ugur, Christian Hake, Hector Romero, Maria Arroyo, Marah Mahmoud, Frederik Lermyte, Heinrich Leonhardt, M Cristina Cardosocentrifugation at 15 000 rpm for 30 min. The cleared lysates were incubated with 2 ml chitin beads (NEB, S6651S) at 4°C with rotation for 3 h to allow CBD-chitin binding. Then beads were washed and treated in benzonase

(7) NUB1 traps unfolded FAT10 for ubiquitin-independent degradation by the 26S proteasomeNature Structural & Molecular BiologySeptember 1, 2025Connor Arkinson, Ken C. Dong, Christine L. Gee, Shawn M. Costello, Aimee Chi Soe, Greg L. Hura, Susan Marqusee, Andreas Martinproteins were eluted with lysis buffer supplemented with 250 mM imidazole and bound to chitin resin (S6651L, New England Biolabs), before washing in lysis buffer and overnight incubation with lysis buffer supplemented

(8) Combinatorial profiling of multiple histone modifications and transcriptome in single cells using scMTR-seqScience advancesAugust 8, 2025Wang Y, Li J, Malcolm AA, Mansfield W, Clark SJ, Argelaguet R, Biggins L, Acton RJ, Andrews S, Reik W, et al.tube was kept on ice. The supernatant of the lysed bacteria was mixed with 5 ml of chitin slurry (NEB, S6651S) and incubated on a rotator overnight at 4°C. The beads were rinsed with 20 ml of HEGX and mixed with

(9) DynaTag for efficient mapping of transcription factors in low-input samples and at single-cell resolutionNature communicationsJuly 28, 2025Hunold P, Pizzolato G, Heramvand N, Kaiser L, Barbiera G, van Ray O, Thomas R, George J, Peifer M, Hänsel-Hertsch R.cleared by centrifugation at 16,000 × g at 4 °C for 30 min. In the meantime, 2.5 mL chitin resin (NEB, S6651S) was packed into Econo-Pac Chromatography Column (BIO-RAD, 732-1010) and washed with 20 mL HEGX buffer.

(10) Nucleosome spacing can fine-tune higher-order chromatin assemblyNat CommunJuly 9, 2025Lifeng Chen, M. Julia Maristany, Stephen E. Farr, Jinyue Luo, Bryan A. Gibson, Lynda K. Doolittle, Jorge R. Espinosa, Jan Huertas, Sy Redding, Rosana Collepardo-Guevara, et al.x g for 30 minutes and the supernatant was recovered. The clarified lysate was then incubated with Chitin Resin (NEB) with rocking for 2 hours. The slurry was then placed in a gravity column and the flow-through

(11) IT-scC&T-seq streamlines scalable, parallel profiling of protein-DNA interactions in single cellsGenome BiolJuly 7, 2025Jingchun Ma, Wei Jin, Li Rong, Zhanyu Gao, Zaman Hazrat, Hosen Md Shakhawat, Fei Long, Zixuan Zhang, Jiandong Huang, Xiaomei Lu, et al.and 30 s off, 40% duty. The cleared pA-Tn5-CBD protein fraction was enriched with chitin resin (NEB, S6651S) at cold-room for 2 h and further washed with 200 ml of HEGX buffer. The Tn5 protein was released by

(12) Iron-Dependent JMJD1A-Mediated Demethylation of H3K9me2 Regulates Gene Expression During Adipogenesis in a Spatial Genome Organization-Dependent MannerGenes CellsApril 28, 2025Shinnosuke Masuda, Tetsuro Komatsu, Safiya Atia, Tomohiro Suzuki, Mayuko Hayashi, Atsushi Toyoda, Hiroshi Kimura, Takeshi Inagakieliminate insoluble residues, the clarified supernatant was incubated with pre‐washed chitin resin (NEB, S6651S) at 4°C for 2 h. The resin was packed into a column (Bio‐Rad, 7,371,517) and extensively washed with

(13) Cryo-EM structures of DNA-free and DNA-bound BsaXI: architecture of a Type IIB restriction-modification enzymeNucleic Acids ResApril 15, 2025Betty W Shen, Dan Heiter, Weiwei Yang, Shuang-Yong Xu, Barry L Stoddardto remove cell debris. Crude supernatants were loaded through two separate 40 ml chitin resin (NEB S6651) columns by gravity, washed with 300 ml of chitin column buffer, and then cleaved over 3 days with 50

(14) An eRNA transcription checkpoint for diverse signal-dependent enhancer activation programsNature GeneticsApril 4, 2025Lishuan Wang, Wei Yuan, Amir Gamliel, Wubin Ma, Seowon Lee, Yuliang Tan, Zeyu Chen, Havilah Taylor, Kenneth Ohgi, Soohwan Oh, et al.glycerol and 0.2% Triton X-100) and centrifuged at 1,000g for 30 min. The supernatant was incubated with Chitin Resin (NEB) for 12 h. CBD-tagged proteins were purified according to the manufacturer’s instructions. The

(15) Fine-tuned interactions between globular and disordered regions of single-stranded DNA binding (SSB) protein are required for dynamic condensation under physiological conditionsProtein SciMarch 27, 2025Zoltán J. Kovács, Péter Ecsédi, Gábor M. Harami, János Pálinkás, Mina Botros, Lamiya Mahmudova, Viktoria Katran, Dávid Érfalvy, Miklós Cervenak, László Smeller, et al.was removed by centrifugation (36,000g, 30 min), and the supernatant was applied to a chitin column (Chitin resin, NEB). After washing, the column was treated with buffer containing 50 mM DTT overnight. Eluted proteins

(16) A combined adjuvant and ferritin nanocage based mucosal vaccine against Streptococcus pneumoniae induces protective immune responses in a murine modelNat CommunMarch 24, 2025Tien Duc Nguyen, Hoang Duy Le, Giang Chau Dang, Hyun Seok Jung, Yoonjoo Choi, Koemchhoy Khim, Young Kim, Shee Eun Lee, Joon Haeng Rheemanufacturer’s instructions, the supernatant was applied to a column filled with chitin agarose beads (Cat: S6651L, New England Biolabs). Optimization and purification of nanocage vaccine For the assembly of the ferritin-tPspA-FlaB

(17) Semi-automated IT-scATAC-seq profiles cell-specific chromatin accessibility in differentiation and peripheral blood populationsNat CommunMarch 17, 2025Wei Jin, Jingchun Ma, Li Rong, Shengshuo Huang, Tuo Li, Guoxiang Jin, Zhongjun Zhou30 s on and 30 s off, 40% duty. The cleared Tn5-CBD protein fraction was enriched with chitin resin (S6651S, NEB) in the cold room for 2 hours and further washed with 200 ml of HEGX buffer. The Tn5 protein was

(18) Role of aspartate 42 and histidine 79 in the aiPLA2 activity and oligomeric status of Prdx6 at low pHSci RepMarch 11, 2025Pushpa Kakchingtabam, Sharifun Shahnaj, Anju Kumari, Japani Longjam, A. N. Wungnaopam, Khundrakpam Herojit Singh, Nasir A. Siddiqui, Rajendrakumar Singh Laishram, Aron B. Fisher, Hamidur Rahamanstandard buffer solutions used for calibrating the pH meter at 25 °C were purchased from Merck (India). Chitin resin beads were obtained from New England Biolabs (NEB) (Ipswich, MA, USA). Ethylenediaminetetraacetic acid

(19) Chemical- and photo-activation of protein-protein thiol-ene coupling for protein profilingCommun ChemJanuary 29, 2025André Campaniҫo, Marcin Baran, Andrew G. Bowie, Daniel B. Longley, Timothy Harrison, Joanna F. McGouransonication tip, for 5 min with a 3-s pulse. The lysate mixture was centrifuged for 45 min, at 13,000 rpm. Chitin resin (5 mL) (New England Biolabs) was added to a column and the system was equilibrated using column buffer

(20) Single-cell mapping of regulatory DNA:Protein interactionsbioRxivJanuary 2, 2025Wei-Yu Chi, Sang-Ho Yoon, Levan Mekerishvili, Saravanan Ganesan, Catherine Potenski, Franco Izzo, Dan Landau, Ivan Raimondifor 40 minutes at 4 °C to precipitate DNA. The supernatant was loaded on a 2-ml chitin column (NEB, S6651S), followed by washing with 12 ml of HEGX. Then, 3 ml of HEGX containing 100 mM DTT was added to the

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Chitin Resin

Chitin Resin from New England Biolabs

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New England Biolabs

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Chitin Resin from New England Biolabs

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