Sepharose CL-2B

21st Aug 2026

CHROMATOGRAPHY RESIN

Sepharose CL-2B

A well-proven cross-linked agarose gel filtration base matrix frequently used for coupling affinity ligands to the matrix.

Catalog No.: Se-500C

Product Overview

Sepharose CL-2B is a well-proven cross-linked agarose gel filtration base matrix and is frequently used for coupling affinity ligands to the matrix.

The matrix is not pre-activated and the user performs all steps in coupling.

Key Advantage: Higher degree of crosslinking improves matrix stability.

Description

Sepharose is a bead-formed agarose-based gel filtration matrix. Sepharose is available with 3 different agarose contents; 2%, 4%, and 6%, designated Sepharose 2B, Sepharose 4B and Sepharose 6B respectively.

Both Sepharose and Sepharose CL have broad fractionation ranges which makes them suitable for characterizing or cleaning-up samples containing components of diverse molecular weight.

Key Characteristics

Matrix 2% agarose
Particle Size 60 μm–200 μm
Recommended Flow Rate <15 cm/h
Recommended Column Height 10 cm
pH Working Range 3–13
CIP Stability pH 2–14

Product Specifications

Specification Details
Product Sepharose CL-2B
Catalog No. Se-500C
Matrix 2% agarose
Particle Size 60 μm–200 μm
Recommended Flow Rate <15 cm/h
Recommended Column Height 10 cm
Maximum Operating Pressure 60–120 cm/h
Pressure Drop 15 cm H₂O / bed height
Bed Height 10 cm
Column Internal Diameter 5 cm
pH Working Range 3–13
CIP Stability pH 2–14
Autoclavable Yes
Sterilization 20 min at 120°C in phosphate buffer, pH 7
Storage 4 to 30°C, 20% Ethanol
Pack Size 1 L

Equilibration

Before applying the sample, equilibrate the column with at least two column volumes of the eluent to be used in the separation, or until the baseline is stable.

Longer equilibration might be needed with detergent solutions. Equilibration is not needed between runs with the same eluent.

Regeneration

Regeneration is normally performed by washing with 2 to 3 column volumes of buffer, followed by re-equilibration in the new buffer if changing conditions.

Sanitization

Wash the column with 0.5 M NaOH.

Sterilization

Autoclavability: 20 min at 120°C in phosphate buffer, pH 7.