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pCDCAR1 CD20 h(γ), T (CAR-T-1-M302-G)

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All products and services are For Research Use Only and CANNOT be used in the treatment or diagnosis of disease.

The vector of anti-CD20 chimeric antigen receptor (CAR) is constructed for the engineering of T cells to target human CD20. The T cells are genetically modified through transduction with a lentiviral vector expressing scFv of anti-CD20 antibody linked to FcεRIγ signaling domains. And the vector product was designed for the treatment of CD20+ malignancies , B-cell lymphoma, mantle cell lymphoma, CD20+ diffuse large cell lymphoma (DLCL), leukemias.

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Details

  • Target
  • CD20
  • Targeting Cell Type
  • T cell
  • Targeting Diseases
  • CD20+ malignancies; B-cell lymphoma; mantle cell lymphoma; CD20+ diffuse large cell lymphoma (DLCL); leukemias
  • Generation
  • First
  • Vector Name
  • pCDCAR1
  • Vector Length
  • 8kb
  • Vector Type
  • Lentiviral
  • Receptor Construction
  • scFv-FcεRIγ
  • Discription of Signaling Cassetes
  • FcεRIγ
    The high-affinity IgE receptor, also known as FcεRI, or Fc epsilon RI, is the high-affinity receptor for the Fc region of immunoglobulin E (IgE). FcεRI is a key molecule involved in allergic reactions. It is a tetramer composed of 1alpha, 1 beta, and 2 gamma chains. The gamma chains are also subunits of other Fc receptors. The scFv-based CARs engineered to contain a signaling domain from FcεRIγ have been shown to deliver a potent signal for T cell activation and function.

Target

  • Clone
  • 1F5
  • Host
  • Mouse
  • Target Species
  • Human
  • Gene Name
  • membrane spanning 4-domains A1
  • Synonyms
  • B1; S7; Bp35; CD20; CVID5; MS4A2; LEU-16; BA0185

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  • Published Data
WB

Fig.1 Detection of 1F5 scFv-Ig by Western blot analysis.

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Fig.1 Detection of 1F5 scFv-Ig by Western blot analysis.

1F5 scFv-Ig from COS cell supernatants were detected by probing Western blots using alkaline phosphatase-conjugated GAH after separating these proteins on reducing (A) and nonreducing (B) SDS-PAGE gels. Neg., Supernatants from cells transfected with pCDM8 vector without inserts.

Daming. S., Oliver. W. P., Theta. T., Martha. S., Hayden, J. A. (1999). Characterization of scFv-Ig Constructs Generated from the Anti-CD20 mAb 1F5 Using Linker Peptides of Varying Lengths1. J Immunol 1 June, 162 (11), 6589-6595.

FCM

Fig.2 1F5 scFv-Ig binding demonstrated by flow cytometry.

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Fig.2 1F5 scFv-Ig binding demonstrated by flow cytometry.

A total of 105 Jurkat or Ramos cells were incubated with PBS or 50 μg/ml 1F5 scFv-Ig for 45 min at 4°C followed by washing and incubation with FITC-labeled GAH for 30 min at 4°C.

Daming. S., Oliver. W. P., Theta. T., Martha. S., Hayden, J. A. (1999). Characterization of scFv-Ig Constructs Generated from the Anti-CD20 mAb 1F5 Using Linker Peptides of Varying Lengths1. J Immunol 1 June, 162 (11), 6589-6595.

ELISA

Fig.3 Binding activity of 1F5 scFv-Ig demonstrated by ELISA.

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Fig.3 Binding activity of 1F5 scFv-Ig demonstrated by ELISA.

A total of 105 Ramos cells were incubated with different concentrations of 1F5 scFv-Ig, followed by incubation with a peroxidase-conjugated GAH second Ab.

Daming. S., Oliver. W. P., Theta. T., Martha. S., Hayden, J. A. (1999). Characterization of scFv-Ig Constructs Generated from the Anti-CD20 mAb 1F5 Using Linker Peptides of Varying Lengths1. J Immunol 1 June, 162 (11), 6589-6595.

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For research use only. Not intended for any clinical use. No products from Creative Biolabs may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative Biolabs.

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