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Empowering Primary Immune Cell Research: High-Efficiency Human CD4⁺/CD8⁺ T Cell and B Cell Sorting

Source: Elabscience®Published: Jan 15,2026

At the forefront of immunological research, whether exploring the precise killing and regulation of T cells or unraveling antibody secretion and antigen presentation by B cells, the foundation of experimentation consistently relies on obtaining primary immune cells of high purity, high viability, and undisturbed physiological function. While traditional positive selection methods can achieve high-purity cells, the binding of antibodies to key cell surface receptors (e.g., CD3, CD4, CD19) can readily alter the cells' native state, potentially impacting downstream functional assays, signaling studies, and even the development of cell-based therapies.

Addressing this critical challenge, the Elabscience® R&D team, leveraging its well-established magnetic bead ‑ based negative selection technology platform, now introduces the Human CD4/CD8 T Cell and B Cell Negative Isolation Kits. Utilizing a negative isolation approach with magnetic beads, these kits eliminate the need for direct labeling of human CD4/CD8 T cells and B cells, thereby avoiding antibody‑induced cell activation or epitope masking. This preserves the cells in their native state, with all surface receptors and molecules (such as CD3/CD28/PD‑1/CD40/BCR, etc.) maintaining their intact, native conformation. These kits represent the golden starting point for functional activation studies, signaling pathway investigations, drug target validation, and cell therapy engineering.

 

Table of Contents

1. Introduction to Cell Isolation Products

2. Features of Cell Isolation Products

3. Experimental Validation Results of Cell Isolation Products

 

01 Introduction to Cell Isolation Products

The Elabscience® Human CD4/CD8 T Cell and B Cell Negative Isolation Kit isolates CD4/CD8 T cells and B cells from fresh human peripheral blood PBMC samples via a negative selection method. Its principle involves labeling non-target cells (non-CD4/CD8 T cells and non-B cells) with different biotin‑conjugated monoclonal antibodies, followed by removal using streptavidin‑coated magnetic beads. This achieves the isolation of human peripheral blood PBMC‑derived CD4/CD8 T cells and B cells. It preserves the unstimulated, native state of the target cells, and the obtained cells are free of any antibody or bead labeling, making them directly suitable for downstream applications. This product series mainly includes the following contents:

Table 1. EasySort™ Human T and B Cell Isolation Kits

Cat. No.

Product Name

Size

Storage

MIH002N

EasySortTM Human CD4+ T Cell Isolation Kit

10/100/200 Assays

2-8°C

MIH003N

EasySortTM Human CD8+ T Cell Isolation Kit

10/100/200 Assays

2-8°C

MIH004N

EasySortTM Human B Cell Isolation Kit

10/100/200 Assays

2-8°C

 

02 Features of Cell Isolation Products

No red blood cell lysis required: ensures better cell viability

No stimulation: target cells are free of antibody or bead labeling, preserving their natural state

High purity: achieves >95% purity post‑selection

No separation column needed: simplifies the workflow

Short processing time: negative selection can be completed in as little as 15 minutes

Broad sample compatibility: suitable for fresh or cryopreserved human PBMC samples

 

03 Experimental Validation Results of Cell Isolation Products

Human CD4 T cell purity increased from 25.42% to 96.92% after negative selection sorting.

Fig. 1 The purity of CD4+ T cells before and after sorting was analyzed by flow cytometry using Elab Fluor® Violet 450 Anti-Human CD3 Antibody [OKT-3] (E-AB-F1001Q) and APC Anti-Human CD4 Antibody [SK3] (E-AB-F1352E). The proportions of CD3⁺CD4⁺ T cells before and after sorting were 25.42% and 96.92%, respectively.

Human CD8 T cell purity increased from 16.97% to 95.79% after negative selection sorting.

Fig. 2 The purity of CD8+ T cells before and after sorting was analyzed by flow cytometry using Elab Fluor® Violet 450 Anti-Human CD3 Antibody [OKT-3] (E-AB-F1001Q) and PE Anti-Human CD8a Antibody [HIT8a] (E-AB-F1271D). The proportions of CD3⁺CD8⁺ T cells before and after sorting were 16.97% and 95.79%, respectively.

Human B cell purity increased from 4.92% to 93.64% after negative selection sorting.

Fig. 3 The purity of human B cells was analyzed by flow cytometry using PerCP Anti-Human CD45 Antibody [HI30] (E-AB-F1137F), PE Anti-Human CD3 Antibody [OKT-3] (E-AB-F1001D), and APC Anti-Human CD19 Antibody [CB19] (E-AB-F1004E). The purity of CD45⁺CD3⁻CD19⁺ human B cells in normal human peripheral blood mononuclear cell samples before and after sorting was 4.92% and 93.64%, respectively.

 

Table 2. T Cell & B Cell Research Products

Product Name

Cat. No.

10×ACK Lysis Buffer

E-CK-A105

Human PBMC Separation Solution(P 1.077)

E-CK-A103

EasySort™ Human CD3+T Cell Isolation Kit

MIH001N

EasySort™-5 Magnet

EC001

Human CD3/CD28 T Cell Activation Beads

MIH001A

CFSE Cell Division Tracker Kit

E-CK-A345

Human Th1/Th2 Flow Cytometry Staining Kit

XJH001

Human Th17 Flow Cytometry Staining Kit

XJH002

Cell Stimulation and Protein Transport Inhibitor Kit

E-CK-A091

Intracellular Fixation/Permeabilization Buffer Kit

E-CK-A109

 

Table 3. Multi‑Color Flow Cytometry Antibodies for T & B Cells

Marker

Clone No.

Fluorochrome

Cat. No.

Application

CD3

OKT-3

Elab Fluor® Violet 450

E-AB-F1001Q

Detection of T cell activation status

CD69

FN50

APC

E-AB-F1138E

CD25

CHI621

PE

AN00360D

HLA-DR

L243

FITC

E-AB-F1111C

CD3

OKT-3

Elab Fluor® Violet 450

E-AB-F1001Q

Human CD4⁺ T‑Cell Detection

CD4

SK3

APC

E-AB-F1352E

CD3

OKT-3

Elab Fluor® Violet 450

E-AB-F1001Q

Human CD8⁺ T‑Cell Detection

CD8

HIT8a

PE

E-AB-F1271D

CD45

HI30

PerCP

E-AB-F1137F

Human B‑Cell Detection

CD3

OKT-3

PE

E-AB-F1001D

CD19

CB19

APC

E-AB-F1004E

 

The above provides an overview of the Elabscience® Human CD4/CD8 T Cell and B Cell Negative Isolation Kit. In the future, Elabscience® will also launch the Human NK Cell Negative Isolation Kit. If you have any questions or require detailed technical documents, please feel free to leave a comment or contact us directly!