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Home -> Products & Services -> CAR Expression Plasmids -> BCMA scFv-CD28-CD3ζ (2nd) CAR Expression Plasmid
 
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BCMA scFv-CD28-CD3ζ (2nd) CAR Expression Plasmid

Item No.: PCAR-086
Shipping: 2 μg
Storage: -20°C

INTRODUCTION

Chimeric Antigen Receptors (CARs) are recombinant receptors that are composed of four regions: an antigen recognition domain (ectodomain), a hinge region, a transmembrane region, and an intracellular T cell signaling domain (endodomain). CAR-T cell therapy uses T cells engineered with CARs to target specific antigen(s) for cancer immunotherapy.

BCMA (also known as TNFRSF17) is a cell surface receptor of the TNF receptor superfamily. It is preferentially expressed in mature B lymphocytes, and may be important for B cell development and autoimmune response. BCMA can specifically bind to the tumor necrosis factor (ligand) superfamily, member 13b (TNFSF13B/TALL-1/BAFF), and to lead to NF-kappaB and MAPK8/JNK activation. BCMA also binds to various TRAF family members, and thus may transduce signals for cell survival and proliferation. BCMA protein is a target of chimeric antigen receptor (CAR) T-cells used in the treatment of multiple myeloma.

RGBiotech offers BCMA scFv-CD28-CD3ζ (2nd) CAR Expression Plasmid to assist CAR-T research. This vector contains a second (2nd) generation of BCMA CAR that consists of four major components: 1) anti-BCMA scFv as an extracellular antigen-binding domain, 2) a hinge region, 3) a transmembrane domain, and 4) CD28 and CD3ζ (CDzeta, CD247) intracellular signaling domains.

HIGHLIGHTS

-Vector Backbone Options: non-viral, or viral (lentiviral, retroviral, AAV, adenoviral)
-Promoter Options: EF1a, CMV, CAG, tissue specific promoter etc.
-Antibiotic Selection Marker Options: puromycin, hygromycin, neomycin, blasticidin, zeocin etc.
-Fluorescent Reporter Options: none, GFP, RFP etc.
-Custom construction is also available based on specific requirements from customer. Please contact us at admin@rgbiotech.com.

APPLICATIONS

-Cell transfection
-Virus production
-Generation of BCMA CAR-T cells

 

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