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N-Hydroxysulfosuccinimide. Protein Modification Agent -Carboxyl group reactive, Forms amine reactive peptides, Needs EDC to mediate. Size: 500mg.

B-Mercaptoethanal. Mild reducing agent for cleaving disulfite bonds. Size: 100mL.

(D,L)-1,4-Dithiothreitol,DTT. Protein Modification Agent-Reducing agent for cleaving disulfide bonds. Size: 5 grams.

HOOK-Biotin Agent. Biotin agent is supplied as individual agent in 500 mg size.

HOOK-NHS-Biotin Agent. Each biotin agent is supplied as individual agent in 50 mg size.

HOOK-NHS-LC-Biotin Agent. Each biotin agent is supplied as individual agent in 50 mg size.

SOURCEâ„¢ 15RPC Reversed Phase Chromatography Media, Cytiva. SOURCEâ„¢ 15RPC Reversed Phase Chromatography Media, GE Healthcare - 17-0727-20, 10 mL, SOURCEâ„¢ 15RPC

SOURCEâ„¢ 30S Ion Exchange Chromatography Media, Cytiva. SOURCEâ„¢ 30S Ion Exchange Chromatography Media, GE Healthcare - 17-1273-01, 50 mL, SOURCEâ„¢ 30S

SOURCEâ„¢ 15Q Ion Exchange Chromatography Media, Cytiva. SOURCEâ„¢ 15Q Ion Exchange Chromatography Media, GE Healthcare - 17-0947-20, 10 mL, SOURCEâ„¢ 15Q

SOURCEâ„¢ 15Q Ion Exchange Chromatography Media, Cytiva. SOURCEâ„¢ 15Q Ion Exchange Chromatography Media, GE Healthcare - 17-0947-01, 50 mL, SOURCEâ„¢ 15Q

SOURCEâ„¢ 30Q Ion Exchange Chromatography Media, Cytiva. SOURCEâ„¢ 30Q Ion Exchange Chromatography Media, GE Healthcare - 17-1275-01, 50 mL, SOURCEâ„¢ 30Q

SOURCEâ„¢ 15S Ion Exchange Chromatography Media, Cytiva. SOURCEâ„¢ 15S Ion Exchange Chromatography Media, GE Healthcare - 17-0944-10, 10 mL, SOURCEâ„¢ 15S

SOURCEâ„¢ 15S Ion Exchange Chromatography Media, Cytiva. SOURCEâ„¢ 15S Ion Exchange Chromatography Media, GE Healthcare - 17-0944-01, 50 mL, SOURCEâ„¢ 15S

SP Sepharoseâ„¢ XL Ion Exchange Chromatography Media, Cytiva. SP Sepharoseâ„¢ XL Ion Exchange Chromatography Media, GE Healthcare - 17-5073-01, 300 mL, SP Sepharoseâ„¢ XL

Q Sepharoseâ„¢ XL Ion Exchange Chromatography Media, Cytiva. Q Sepharoseâ„¢ XL Ion Exchange Chromatography Media, GE Healthcare - 17-5072-01, 300 mL, Q Sepharoseâ„¢ XL

Glutathione Sepharoseâ„¢ 4B Affinity Chromatography Media, Cytiva. Glutathione Sepharoseâ„¢ 4B Affinity Chromatography Media, GE Healthcare - 17-0756-05, 100 mL, Glutathione Sepharoseâ„¢ 4B

NHS Mag Sepharose, Cytiva - 28-9440-09, 500 µL

Protein G Mag Sepharose, Cytiva - 28-9440-08, 500 µL

Protein A Mag Sepharose, Cytiva - 28-9440-06, 500 µL

NHS Mag Sepharose, Cytiva - 28-9513-80, 4 x 500 µL

Protein G Mag Sepharose, Cytiva - 28-9513-79, 4 x 500 µL

Protein A Mag Sepharose, Cytiva - 28-9513-78, 4 x 500 µL

Desalting Column And Resin 1 Set.

Protein A Mag Sepharose Xtra 2.

Protein A Mag Sepharose Xtra 5.

Protein G Mag Sepharose Xtra 2.

Protein G Mag Sepharose Xtra 5.

His Mag Sepharose Ni 2x1 mL.

His Mag Sepharose Ni 5x1mL.

Captoâ„¢ Core 700 Multimodal Chromatography Media, Cytiva. Captoâ„¢ Core 700 Multimodal Chromatography Media, GE Healthcare - 17548101, 25 mL, Captoâ„¢ Core 700

Captoâ„¢ Core 700 Multimodal Chromatography Media, Cytiva. Captoâ„¢ Core 700 Multimodal Chromatography Media, GE Healthcare - 17548102, 100 mL, Captoâ„¢ Core 700

HiScreen Capto Core 700 Prepacked 4.7 ml Column. For intermediate purification and polishing of large molecules in flow-through mode. Each bead has ligand-activated core and outer layer without ligands preventing large targets from entering the beads.

Concanavalin A AGAR .75ML PK10. Concanavalin A Agarose consists of Con A coupled to 4% agarose by the cyanogen bromide method. Con A is a tetrameric metalloprotein lectin isolated from Canavalia ensiformis (jack bean).

RESIN IMMOB REDUCTANT 2ML F/PRT/PEPTIDE - 786-148

Immobilized metal affinity chromatography. (IMAC) resin utilizing nickel (Ni2+) for the purification of 6x histidine tagged proteins.

Captoâ„¢ L Affinity Chromatography Media, Cytiva. Captoâ„¢ L Affinity Chromatography Media, GE Healthcare - 17547801, 25 mL, Captoâ„¢ L

Captoâ„¢ L Affinity Chromatography Media, Cytiva. Captoâ„¢ L Affinity Chromatography Media, GE Healthcare - 17547802, 200 mL, Captoâ„¢ L

Captoâ„¢ L Affinity Chromatography Media, Cytiva. Captoâ„¢ L Affinity Chromatography Media, GE Healthcare - 17547806, 5 mL, Captoâ„¢ L

HiScreen Capto L Columns, Cytiva - 17-5478-14, 4.7 ml, HiScreenâ„¢ Captoâ„¢ L

Ready to use ion exchange column. Pre-packed with Capto adhere ImpRes multimodal medium.The column is an excellent choice for method optimization and parameter screening.The multimodal functionality gives a different selectivity compared with traditional ion exchange columns

Ready to use ion exchange column. Pre-packed with Capto adhere ImpRes multimodal medium.The column is an excellent choice for method optimization and parameter screening.The multimodal functionality gives a different selectivity compared with traditional ion exchange columns

Capto adhere ImpRes is a multimodal anion exchange medium. For intermediate purification and polishing of monoclonal antibodies after the Protein A capture step,giving the possibility to design a two step chromatographic downstream process T

Capto adhere ImpRes is a multimodal anion exchange medium. For intermediate purification and polishing of monoclonal antibodies after the Protein A capture step,giving the possibility to design a two step chromatographic downstream process

Capto adhere ImpRes is a multimodal cation exchange medium. With a different selectivity,compared with traditional ion exchangers.It can be used to bind proteins at the conductivity of the feed material and to solve specific purification challenges.T

Capto adhere ImpRes is a multimodal cation exchange medium. With a different selectivity,compared with traditional ion exchangers.It can be used to bind proteins at the conductivity of the feed material and to solve specific purification challenges.

Ni Sepharose Excel. Is A 90 Um Highly Cross-Linked Agarose Imac Medium Precharged With Nickel Ions Exceptionally Strongly Bound To A Chelating Ligand.

Sephadex G-10. Sephadex G-25 is the first choice for desalting faster and safer than dialysis.Sephadex G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.100 g

Sephadex G-10. Sephadex G-25 is the first choice for desalting faster and safer than dialysis.Sephadex G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.500 g

Sephadex G-15. Sephadex G-25 is the first choice for desalting faster and safer than dialysis.Sephadex G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.100 g

Sephadex G-25 Superfine. Sephadex G-25 is the first choice for desalting faster and safer than dialysis.Sephadex G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.100 g

Sephadex G-25 Fine. Sephadex G-25 is the first choice for desalting faster and safer than dialysis.Sephadex G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.100 g

Sephadex G-25 Fine. Sephadex G-25 is the first choice for desalting faster and safer than dialysis.Sephadex G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.500 g

Sephadex G-25 Medium. Sephadex G-25 is the first choice for desalting faster and safer than dialysis.Sephadex G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.100 g

Sephadex G-25 Medium. Sephadex G-25 is the first choice for desalting faster and safer than dialysis.Sephadex G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.500 g

Sephadex G-25 Coarse. Sephadex G-25 is the first choice for desalting faster and safer than dialysis.Sephadex G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.100 g

Sephadex G-25 Coarse. Sephadex G-25 is the first choice for desalting faster and safer than dialysis.Sephadex G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.500 g

Sephadex G-50 Superfine. Sephadex G-25 is the first choice for desalting faster and safer than dialysis.Sephadex G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.100 g

Sephadex G-50 Fine. Sephadex G-25 is the first choice for desalting faster and safer than dialysis.Sephadex G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.100 g

Sephadex G-50 Fine. Sephadex G-25 is the first choice for desalting faster and safer than dialysis.Sephadex G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.500 g

Sephadex G-50 medium. Sephadex G-25 is the first choice for desalting faster and safer than dialysis.Sephadex G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.100 g

Sephadex G-50 medium. Sephadex G-25 is the first choice for desalting faster and safer than dialysis.Sephadex G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.500 g

Sephadex G-75. Sephadex G-25 is the first choice for desalting faster and safer than dialysis.Sephadex G-25 is ideal for buffer exchange and for removal of free label, e.g..The classic gel filtration medium.100 g

Sephadex G-75 Superfine. Well-proven and widely used in industrial processes.Proven batch-to-batch reproducibility for more than 30 years. Wide selection of separation ranges.Hydrophilic backbone gives low non-specific interactions plus excellent recoveries.Economical.100 g

Sephadexâ„¢ G-100 Gel Filtration Media, Cytiva. Sephadexâ„¢ G-100 Gel Filtration Media, GE Healthcare - 17-0060-01, 100 g, Sephadexâ„¢ G-100

Sephadexâ„¢ G-100 Gel Filtration Media, Cytiva. Sephadexâ„¢ G-100 Gel Filtration Media, GE Healthcare - 17-0061-01, 100 g, Sephadexâ„¢ G-100 Superfine

Sephadex LH-20. Excellent for fractionation of lipids, hormones, vitamins, and other small biomolecules. Designed for use in polar organic solvents and aqueous solvent mixtures.Since Sephadex LH-20 has such unique properties, we recommend that you consult the publications 100 g

Sephadex LH-20. Excellent for fractionation of lipids, hormones, vitamins, and other small biomolecules. Designed for use in polar organic solvents and aqueous solvent mixtures.Since Sephadex LH-20 has such unique properties, we recommend that you consult the publications 500 g

Sephadex LH-20. Excellent for fractionation of lipids, hormones, vitamins, and other small biomolecules. Designed for use in polar organic solvents and aqueous solvent mixtures.Since Sephadex LH-20 has such unique properties, we recommend that you consult the publications 25 g

DEAE Sephadex A-25. High binding capacities for column or batch techniques Proven batch-to-batch reproducibility for more than 30 years Very high capacities even at elevated ionic strengths Hydrophilic backbone gives low non-specific binding and high recoveries

DEAE Sephadex A-50. High binding capacities for column or batch techniques Proven batch-to-batch reproducibility for more than 30 years Very high capacities even at elevated ionic strengths Hydrophilic backbone gives low non-specific binding and high recoveries

CM Sephadex C-25. High binding capacities for column or batch techniques Proven batch-to-batch reproducibility for more than 30 years Very high capacities even at elevated ionic strengths Hydrophilic backbone gives low non-specific binding and high recoveries

CM Sephadex C-50. 500 g

CNBr-activated Sepharose 4B is an established cyanogen bromide-activated medium used for more than twenty years and documented with many references.Multi-point attachment of protein ligands minimizes leakage of coupled ligand.Easy, rapid and efficient coupling.15 g

Con A Sepharose 4B. Immobilized Concanavalin A is useful for isolating mannose- and glucose-containing glycoproteins.To select the optimum lectin for purification, screen different lectin media, e.g. Con A Sepharose 4B and Lentil Lectin Sepharose 4B.100 ml

Con A Sepharose 4B. Immobilized Concanavalin A is useful for isolating mannose- and glucose-containing glycoproteins.To select the optimum lectin for purification, screen different lectin media, e.g. Con A Sepharose 4B and Lentil Lectin Sepharose 4B.5 ml

Lentil Lectin Sepharose 4B purifies glycoproteins, including detergent-solubilized membrane glycoproteins and viral glycoproteinsRetains binding ability in the presence of detergentsTo select the optimum lectin for purification, screen different lectin media 25 ml

Epoxy-activated Sepharose 6B is for coupling ligands that contain hydroxyl, amino or thiol groups.Long hydrophilic, uncharged spacer arms eliminate non-specific interactions and make the oxirane groups available for coupling.15 g

DEAE Sephacel. 500 ml

Calmodulin Sepharose 4B. For single-step purification of calmodulin-binding peptide fusion proteins.Suitable for tandem affinity purification (TAP) of protein complexes.Purification of calmodulin-regulated proteins from all eukaryotic cells.10ml

EAH Sepharose 4B is for coupling aldehyde- or carboxyl acid group containing ligands.Long spacer arms make the primary groups easily available for coupling.Ligand coupling results in stable amine or amide linkages.50 ml

illustra Sephadex G-50 DNA Grade F. For purification of DNA from small molecules by gel filtration.Tested to ensure reproducibly high recovery of DNA.Sephadex G-50 DNA Grade is used in AutoSeq G-50 columns, ProbeQuant G-50 Micro Columns, MicroSpin G-50 Columns and NICK Columns.100 g

illustra Sephadex G-100 DNA Grade SF. For purification of DNA from small molecules by gel filtration.Tested to ensure reproducibly high recovery of DNA.Sephadex G-50 DNA Grade is used in AutoSeq G-50 columns, ProbeQuant G-50 Micro Columns, MicroSpin G-50 Columns and NICK Columns..100 g

Chelating Sepharose Fast Flow. Iminodiacetic acid coupled to Sepharose Fast Flow for purification of histidine-tagged proteins via metal ion complex formation.50 ml

Sephacryl S-200 HR. Maximum recovery and minimum nonspecific adsorption with long-term chemical and physical stability resulting from the hydrophilic, rigid allyl dextran/ bisacrylamide matrix.

Sephacryl S-200 HR. Maximum recovery and minimum nonspecific adsorption with long-term chemical and physical stability resulting from the hydrophilic, rigid allyl dextran/ bisacrylamide matrix.

Sephacryl S-300 HR. Maximum recovery and minimum nonspecific adsorption with long-term chemical and physical stability resulting from the hydrophilic, rigid allyl dextran/ bisacrylamide matrix.

Sephacryl S-300 HR. Maximum recovery and minimum nonspecific adsorption with long-term chemical and physical stability resulting from the hydrophilic, rigid allyl dextran/ bisacrylamide matrix.

Sephacryl S-400 HR. Maximum recovery and minimum nonspecific adsorption with long-term chemical and physical stability resulting from the hydrophilic, rigid allyl dextran/ bisacrylamide matrix.

Sephacryl S-400 HR. Maximum recovery and minimum nonspecific adsorption with long-term chemical and physical stability resulting from the hydrophilic, rigid allyl dextran/ bisacrylamide matrix.Sephacryl S-100 HR is designed for separating peptides and small proteins.

Sephacryl S-100 HR. Maximum recovery and minimum nonspecific adsorption with long-term chemical and physical stability resulting from the hydrophilic, rigid allyl dextran/ bisacrylamide matrix.

Sephacryl S-100 HR. Maximum recovery and minimum nonspecific adsorption with long-term chemical and physical stability resulting from the hydrophilic, rigid allyl dextran/ bisacrylamide matrix.

Sephacryl S-500 HR. Maximum recovery and minimum nonspecific adsorption with long-term chemical and physical stability resulting from the hydrophilic, rigid allyl dextran/ bisacrylamide matrix.

Sephacryl S-500 HR. Maximum recovery and minimum nonspecific adsorption with long-term chemical and physical stability resulting from the hydrophilic, rigid allyl dextran/ bisacrylamide matrix.

Protein G Sepharose 4 Fast Flow. Protein G media exhibit binding specificities that are complementary to Protein A media Bind a broad range of species and subclasses of IgG High purity is assured due to the strong affinity between protein G and the target IgG 5 ml

Protein G Sepharose 4 Fast Flow. Protein G media exhibit binding specificities that are complementary to Protein A media Bind a broad range of species and subclasses of IgG High purity is assured due to the strong affinity between protein G and the target IgG

Protein G Sepharoseâ„¢ 4 Fast Flow Affinity Chromatography Media, Cytiva. Protein G Sepharoseâ„¢ 4 Fast Flow Affinity Chromatography Media, GE Healthcare - 17-0618-05, 200 mL, Protein G Sepharoseâ„¢ 4 Fast Flow

DEAE Sepharoseâ„¢ CL-6B Ion Exchange Chromatography Media, Cytiva. DEAE Sepharoseâ„¢ CL-6B Ion Exchange Chromatography Media, GE Healthcare - 17-0710-01, 500 mL, DEAE Sepharoseâ„¢ CL-6B

Glutathione Sepharose 4B. 10ml,For single-step purification of recombinant derivatives of glutathione S-transferase and glutathione-dependent proteins,Binding capacity: 5mg horse liver GST/mL, Average particle size: 90um

Glutathione Sepharose 4B. Fast and simple purification of GST-tagged proteins.

Protein A Sepharose CL-4B. The classic Protein A Sepharose CL-4B is well documented for immunoglobin purification and fractionation and is suitable for immunoprecipitation procedures.Strong binding to Fc region of IgG.Ideal for polyclonal antibody purification.High capacity20 mg human IgG/ml.1.5 g

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