Skip to Content
Books & Reference Materials
Category Image
Extraction Systems
Category Image
Industrial Instruments
Category Image
Glassware & Plasticware
Category Image
Transfection & Cloning
Category Image
Laboratory Quality Control Solutions
Category Image
Entomology Supplies
Category Image
Sample Preparation
Category Image

Lymphoprep™

(0 review)
SKU: 1858-1
UoM: Each
Inquiry Required

  • Pack Size
Store Availability & Pickup
LabMart Limited - Tamale
NS-246, Via, 4388 Tamale-Kumbungu Rd, Tamale, Northern Region, Ghana
Not available
LabMart Limited
10 Rcecourse street, Accra, Greater Accra Region, Ghana
1 available
Add to quote
MOQ : 1.0 Each
Estimated delivery Estimated delivery: 3-5 business days
Telecel AirtelTigo Maestro Mastercard Visa MTN

A simple and effective method for the isolation of mononuclear cells from human blood was reported by Dr. Arne Boyum in 1968. For more than 35 years a commercial medium known as LymphoprepTM has been widely used for isolating these cells.

Mononuclear cells (monocytes and lymphocytes) have a lower buoyant density than the erythrocytes and the polymorphonuclear (PMN) leukocytes (granulocytes). The vast majority of mononuclear cells have densities below 1.077 g/ml. These cells can therefore be isolated by centrifugation on an isoosmotic medium with a density of 1.077 g/ml, which allows the erythrocytes and the PMNs to sediment through the medium while retaining the mononuclear cells at the sample/medium interface.

The described method is rapid, simple and reliable and gives excellent results with blood samples from normal individuals and patients.

To obtain the maximum yield it is important that the blood sample is diluted 1:1 with physiological saline before being applied to the gradient. The contamination of erythrocytes in the mononuclear cell suspension is usually between 3-10% of the total cell number.

Some immature PMNs may band with the lymphocytes during intense immunosuppressive therapy. When heparinised blood is used, it is essential to remove most of the platelets, in order to avoid inhibition in the cytotoxicity test. Each batch of Lymphoprep is checked on the level of endotoxins using a specific LAL test. The goal is to provide batches with an endotoxin level lower or equal to 0.13 IU/ml.

For every batch produced a Certificate of Analysis showing the actual values of density, osmolality and endotoxins is made available upon request. We also claim sterility according to Ph.Eur.

Lymphoprep is manufactured, packed and released in compliance with GMP and ISO 13485.

LymphoprepTM can be used for the preparation of pure lymphocyte suspensions for tissue typing, antilymphocyte sera and immunological research. Thorsby and Brattelie used this technique with only slight modifications in the preparation of pure lymphocyte suspensions for cytotoxicity tests and lymphocyte cultures.

Application: Cell Separation
Storage Temperature: Room Temperature
Product Type: Cell Density Medium
Product Grade: Molecular Biology

A simple and effective method for the isolation of mononuclear cells from human blood was reported by Dr. Arne Boyum in 1968. For more than 35 years a commercial medium known as LymphoprepTM has been widely used for isolating these cells.

Mononuclear cells (monocytes and lymphocytes) have a lower buoyant density than the erythrocytes and the polymorphonuclear (PMN) leukocytes (granulocytes). The vast majority of mononuclear cells have densities below 1.077 g/ml. These cells can therefore be isolated by centrifugation on an isoosmotic medium with a density of 1.077 g/ml, which allows the erythrocytes and the PMNs to sediment through the medium while retaining the mononuclear cells at the sample/medium interface.

The described method is rapid, simple and reliable and gives excellent results with blood samples from normal individuals and patients.

To obtain the maximum yield it is important that the blood sample is diluted 1:1 with physiological saline before being applied to the gradient. The contamination of erythrocytes in the mononuclear cell suspension is usually between 3-10% of the total cell number.

Some immature PMNs may band with the lymphocytes during intense immunosuppressive therapy. When heparinised blood is used, it is essential to remove most of the platelets, in order to avoid inhibition in the cytotoxicity test. Each batch of Lymphoprep is checked on the level of endotoxins using a specific LAL test. The goal is to provide batches with an endotoxin level lower or equal to 0.13 IU/ml.

For every batch produced a Certificate of Analysis showing the actual values of density, osmolality and endotoxins is made available upon request. We also claim sterility according to Ph.Eur.

Lymphoprep is manufactured, packed and released in compliance with GMP and ISO 13485.

LymphoprepTM can be used for the preparation of pure lymphocyte suspensions for tissue typing, antilymphocyte sera and immunological research. Thorsby and Brattelie used this technique with only slight modifications in the preparation of pure lymphocyte suspensions for cytotoxicity tests and lymphocyte cultures.

Lymphoprep protocol.pdf
This will display Shipping & Return.

A simple and effective method for the isolation of mononuclear cells from human blood was reported by Dr. Arne Boyum in 1968. For more than 35 years a commercial medium known as LymphoprepTM has been widely used for isolating these cells.

Mononuclear cells (monocytes and lymphocytes) have a lower buoyant density than the erythrocytes and the polymorphonuclear (PMN) leukocytes (granulocytes). The vast majority of mononuclear cells have densities below 1.077 g/ml. These cells can therefore be isolated by centrifugation on an isoosmotic medium with a density of 1.077 g/ml, which allows the erythrocytes and the PMNs to sediment through the medium while retaining the mononuclear cells at the sample/medium interface.

The described method is rapid, simple and reliable and gives excellent results with blood samples from normal individuals and patients.

To obtain the maximum yield it is important that the blood sample is diluted 1:1 with physiological saline before being applied to the gradient. The contamination of erythrocytes in the mononuclear cell suspension is usually between 3-10% of the total cell number.

Some immature PMNs may band with the lymphocytes during intense immunosuppressive therapy. When heparinised blood is used, it is essential to remove most of the platelets, in order to avoid inhibition in the cytotoxicity test. Each batch of Lymphoprep is checked on the level of endotoxins using a specific LAL test. The goal is to provide batches with an endotoxin level lower or equal to 0.13 IU/ml.

For every batch produced a Certificate of Analysis showing the actual values of density, osmolality and endotoxins is made available upon request. We also claim sterility according to Ph.Eur.

Lymphoprep is manufactured, packed and released in compliance with GMP and ISO 13485.

LymphoprepTM can be used for the preparation of pure lymphocyte suspensions for tissue typing, antilymphocyte sera and immunological research. Thorsby and Brattelie used this technique with only slight modifications in the preparation of pure lymphocyte suspensions for cytotoxicity tests and lymphocyte cultures.

Lymphoprep protocol.pdf

This will display Shipping & Return.

Specifications

Pack Size 1 x 500 mL, 6 x 500 mL, 1 x 250 mL, 4 x 250 mL