Catalog Products » CytoSinct™ TCR αβ Nanobeads, human (GMP)

CytoSinct™ TCR αβ Nanobeads, human (GMP)

CytoSinct TCR αβ Nanobeads, human (GMP) is intended for the in vitro magnetic labeling for pre-separation, removal or other processing of human TCR αβ positive cells from heterogeneous cell populations for instance leukapheresis samples or expanded TCR αβ knockout cell cultures, enabling further cultivation, genetic modification or other processing of the cells.
L00952
$1000.00

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Overview
Product Description CytoSinct TCR αβ Nanobeads, human (GMP) is intended for the in vitro magnetic labeling for pre-separation, removal or other processing of human TCR αβ positive cells from heterogeneous cell populations for instance leukapheresis samples or expanded TCR αβ knockout cell cultures, enabling further cultivation, genetic modification or other processing of the cells.

Properties
Capacity
Catalog number SizeCapacity
L009527.5 mLUp to 8×109 target cells from up to 2×1010 total cells
Composition Colloidal solution of iron-dextran nanobeads conjugated to monoclonal TCR αβ antibody in PBS buffer stabilized with HSA and Poloxamer 188
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°C

Regulatory and legal notes

Warnings and precautions
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
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.