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目錄產品 » CytoSinct? CD8 Nanobeads, human (GMP)

CytoSinct? CD8 Nanobeads, human (GMP)

The CytoSinct CD8 Nanobeads, human (GMP) is used for in vitro isolation or depletion CD8+ cells from fresh or frozen peripheral blood mononuclear cells (PBMCs), leukapheresis products or single cell suspension based on the surface expression of human CD8. Due to the nanoscale structure of the CytoSinct CD8 Nanobeads, human (GMP), the excess reagent can be removed by centrifugation or conventional supernatant replacement.
L00933
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Product Description The CytoSinct CD8 Nanobeads, human (GMP) is used for in vitro isolation or depletion CD8+ cells from fresh or frozen peripheral blood mononuclear cells (PBMCs), leukapheresis products or single cell suspension based on the surface expression of human CD8. Due to the nanoscale structure of the CytoSinct CD8 Nanobeads, human (GMP), the excess reagent can be removed by centrifugation or conventional supernatant replacement.

Capacity
Catalog number SizeCapacity
L00933-7.57.5 mLUp to 4×109 target cells from up to 4×1010 total cells.
Composition Colloidal solution of iron-dextran nanobeads conjugated to monoclonal CD8 antibody in PBS buffer stabilized with HSA and Poloxamer 1883
Endotoxin Content <2 EU/mL as determined by Limulus Amebocyte Lysate (LAL) limit assay (USP <85>)
Sterility Sterility is tested and confirmed according to USP <71>
Storage & Stability Store at 2-8 ℃


Warnings and precautions 1. Do not freeze.
2. The product is intended for in vitro use only. Not for intravenous infusion.
3. Any clinical application of the separated cells is exclusively within the responsibility of the user.
4. Do not use after the expiry date printed on the product label.
5. Do not use it if the package is damaged. Use reagent only if the vial is undamaged and sealed.
6. Do not reuse.
7. The product is not recommended for use with patients known or suspected to have sensitivity against mouse immunoglobulins or iron-dextran.
8. Patients may develop human anti-mouse antibodies (HAMA).

Instructions for use 1. Label cells at room temperature for 30 minutes.
2. Work under sterile conditions.
3. The capacity given is for reference. Optimizing the process according to actual requirements is recommended.


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