Leuko 24+ Spin Medium

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Leuko 24+ Spin density gradient medium, sterile, ready-to-use solution for the in vitro isolation of all leukocytes from more than 12h old sample material (whole blood or buffy coat).

40.00 € 40.0 EUR 40.00 €

109.00 €

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  • Variant
  • Sterility
  • Species
  • Cell separation platform
  • Cell separation method
  • Manufacturer
  • Terms of delivery
  • Storage condition
  • Storage condition
  • Regulatory statement

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Catalog No. 60-00096-10

Terms & Conditions
All ordering information can be found here


HS Code: 38229000

Details,  Leuko 24+ Spin Medium

Leuko 24+ Spin density gradient medium is a sterile, ready-to-use solution for the isolation of human leukocytes from more than 12 h old sample material (whole blood or buffy coat) with high yield. Mononuclear and polymorphonuclear cells can be enriched with Leuko 24+ Spin Density Medium by simple density gradient centrifugation. When Leuko 24+ is combined with PBMC 24+ Spin Density Medium, the leukocyte population can be separated directly into PBMC and multinucleated cells. 

Specification

Target cells

all leukocytes

Separation density cut-off

1,088 g/ml

Cell separation method

negative


Sample material

Human whole blood, Buffy Coat

Compatibility with

pluriMate, SepMate, LeucoSep

Can be used with

pluriSpin, MACS, EasySep, RosetteSep, MojoSort

Features

Access to older sample material

Leuko 24+ Spin Medium enables the enrichment of cells from sample material that is already older than 12 hours. 

Replace

Alternative products, such as GranuloSep, Pancoll or Histopaque - 1119, for the enrichment of leukocytes can be substituted with Leuko Spin.

Compatible

The enriched cells can be used for downstream applications such as MACS, SepMate, RosetteSep, MojoSort .

Combinable

The pluriSpin separation media can be combined with each other and can be used, for example, as a double gradient for the simultaneous enrichment of two cell populations. 

Separation Scheme

First, the sample material is carefully layered onto the Leuko Spin density gradient medium. Mixing of the two phases must be avoided. After density gradient centrifugation, the upper layer (plasma and dilution buffer) is aspirated. The two layers of leukocytes are then transferred to a new tube and the cells are washed.

Tip! Use pluriMate tubes. 

For overlaying the dense medium, we recommend our pluriMate tubes. The integrated barrier of the pluriMate tubes prevents mixing of the two phases (sample material and separation medium) and allows the enriched cells to be poured off after the first centrifugation step. They save time and increase the reproducibility of the results.  

Preparation of PBMC with PBMC Spin Medium. The sample material (1) is carefully placed on the PBMC spin medium (2).

BEFORE

Preparation of leukocytes with Leuko Spin Medium. The sample material (1) is carefully placed on the Leuko Spin Medium (2).

AFTER

Layers after centrifugation. After centrifugation, the leukocytes form two white layers on the Leuko Spin Medium (4). Layer (2) consists of mononuclear leukocytes and layer (3) of polymorphonuclear leukocytes (granulocytes). Cells with a higher density, such as erythrocytes, and dead cells pass through the medium and are located at the bottom of the tube (4).

pluriSelect, density gradient separation media.

Cell separation. simple. fast. uncomplicated.

Other separatation media

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Product specification

Information
Variant 1 BTL, 100 ml or 1 BTL, 250 ml or 1 BTL, 500 ml
Sterility sterile
Species Human
Cell separation platform non-magnetic
Cell separation method negative
General information
Manufacturer pluriSelect
Terms of delivery ambient temperature
Storage condition room temperature, protected from light
Regulatory statement For research use only. Not for use in diagnostic procedures.