Sephadex® G-100 - Medium , CAS No.9050-94-6

CAS: 9050-94-6 Cat. No.: S665614
AVAILABLE TO ORDER
GRADE & PURITY Medium
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
10g
S665614-10g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$699.90
50g
S665614-50g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$2,699.90
Enter a quantity for the sizes you want to add.
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Why this grade

Medium for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Dextran gel is a kind of bead gel, which contains a lot of hydroxyl groups and swells easily in water and electrolyte solution. Hydrophilic matrix minimizes its non-specific adsorption, and achieves high recovery rate during biomolecule separation. G-type dextran gels have different crosslinking degrees, so their swelling degree and fractionation range are also different. The swelling degree of dextran gel is basically unaffected by the presence of salt and detergent.

Instructions for use:  exist in the form of dry powder, which must be swelled before use. Excessive stirring should be avoided during swelling, because it may damage the filler. Do not use magnetic stirrer.

I. Preparation of filler

(1) expand the filler in excess deionized water or buffer solution at room temperature for 24 hours, or expand it with hot water for 1 hour (do not take a water bath! )。

Elution buffer should not contain high viscosity reagents. If there are floating objects on the upper layer during swelling, please remove them.

(2) Balance the swelling filler, all buffers and other materials to the experimental operating temperature, and degas all buffers.

Two-pack column

(1) check whether all components of the chromatographic column, especially the filter screen, sealing ring and screw plug are tight, and whether the glass tube is clean and complete.

(2) Wet the column and the bottom of the column with water or buffer and keep the liquid level for a short period of time, so that there is no bubble at the bottom.

(3) Use a glass rod to guide the homogenate to be poured into the column at one time along the inner wall of the column, taking care not to generate bubbles. Open the liquid outlet of the column to make gel

Settle freely in the column, and connect the top stigma of the column.

(4) Open the peristaltic pump, and let the buffer flow through at a flow rate which is 1.33 times of the flow rate when in use, so as to stabilize the column bed (pay attention not to exceed the filling pressure)

Material maximum pressure resistance).

Three equilibria

Balance the chromatographic column at least 5-10 column volumes before loading until the baseline of the recorder becomes stable (pH value and conductance value of effluent are equal to

PH value and conductance value of Buffer on the upper column).

Four samples

Samples must be centrifuged or filtered (0.45um filter membrane).

Generally, the loading amount of gel filtration is not more than 5% of the column bed volume, and we suggest that the initial loading should be controlled at 1-2% of the column bed volume, depending on the score

From the situation can be adjusted; When desalting, the loading amount can reach 20% of the column bed volume, and the selection of column height is also related to the separation requirements. The higher the column, the higher the separation

The better the separation effect is, however, the gel column with too high column height will cause large back pressure, which should be avoided as much as possible. Difficult to separate substances must have certain

Column height and flow rate are controlled, and the ratio of height to diameter during desalination is 5: 1.

Five elution methods

It can be eluted with saline-free solution or buffer solution during column loading.

Six cleaning in place (CIP)

CIP is performed once after the gel is used ten times, in order to remove the precipitated and stubborn residual protein in the column bed. The method is to oxidize with 0.1 M hydrogen

2 column volumes were washed with sodium, and then regenerated with at least 10 column volumes of equilibrium buffer.

Add notes:

(1) before loading, the sample must be filtered by membrane and pigment removed, otherwise impurities and pigment will be adsorbed on the filler and affect the filler

Normal use. All buffers need to be filtered with a 0.45um filter.

(2) Avoid using strong acid and alkali with high concentration, and the concentration of acid and alkali should be lower than 0.1 mol. Alkali slows down the flow rate.

(3) Different samples have different adsorption and elution methods, which can be carried out according to relevant literatures.

Save notes:

Untreated filler shall be sealed at room temperature. After using the filler, wash the salt thoroughly with pure water, and finally store it in 20% ethanol at 4℃

Save.

Sephadex is a gel filtration support prepared by cross-linking dextran with trichloroacetic acid. Different types of Sephadex have different degrees of cross-linking, and thus their swelling degree and molecular separation range are also different. There are five different G types, including G-10 for small molecules to G-75 for large molecules. Sephadex G-10 is one of them. Sephadex G-50 has four different particle sizes (coarse, filler, fine, and ultra-fine), with Superfine having the smallest particle size and being able to achieve more efficient separation through a shorter diffusion distance. For large-scale group separation that requires high flow rate and low operating pressure, coarse particle fillers are preferred.

Specifications

Specifications & Purity
Medium
Legal Information
Sephadex is a registered trademark of Cytiva
Storage
Store at 2-8°C, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot NumberCertificate TypeDateItem
F2601417Certificate of AnalysisMay 19, 2026 S665614
F2601418Certificate of AnalysisMay 19, 2026 S665614
Chemical and Physical Properties
SensitivityMoisture sensitive
Flash Point(°C)38 °C
Documents & Articles
Citations of This Product
References
1. Meimei Fu, Qianru Xiang, Zhuoyi Huang, Wenjun Luo, Zhou Fang, Jintao Li, Yue Li, Zijun Xia, Yangjia Huang, Yitao Zhao, Wenzhen Liao, Jinshan Guo.  (2025)  Photo-Cross-Linked and Photothermal Flammulina velutipes Polysaccharide Hydrogel Loaded with Caffeic Acid-Copper Nanozyme for Diabetic Wound Healing.  ACS Applied Materials & Interfaces,      [PMID:40952936] [10.1021/acsami.5c11453]
2. Fang Long, Zuomin Hu, Huanzhao Luo, Zhongxing Chu, Shuqin Li, Yaping Zhou, Anping Li, Feijun Luo.  (2026)  Remodeling of Bamboo (Phyllostachys edulis) Shoot Polysaccharides by Monascus purpureus Fermentation Enhances Antioxidant Protection in Caco-2 Cells.  Foods,  15  (4): (704).  [PMID:41750896] [10.3390/foods15040704]
Solution Calculators
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