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Your Position: Home > Solutions for In Vivo CAR-T Cell Therapy Development

In vivo CAR T cell therapy is advancing into clinical trials! This groundbreaking approach aims to reprogram immune cells directly inside the body, offering a faster, more cost-effective, and potentially safer alternative to traditional ex vivo CAR T therapies.

Faster treatment timeline: Off-the-shelf reprogramming cassettes make in vivo CAR-T therapy weeks faster than ex vivo methods.
 Cost-effective: The estimated cost per dose could be as low as $5,000—a fraction of current CAR-T therapy costs.
 Improved patient outcomes: Patients retain intact immune systems, as there's no need for harsh chemotherapy regimens, and less exhausted immune cells could be more effective at fighting cancer.
Trends Pharmacol Sci. 2024;45(5):406-418.

Trends Pharmacol Sci. 2024;45(5):406-418.

Discovery & Development
Lead Abs screening
CAR-encoding DNA or mRNA payload design
Design of delivery system
In vitro and in Vivo efficacy testing
Toxicity studies
CMC
Plasmid DNA production
mRNA production and purification
Formulation and Characterization of ab-LNPs
Fill & Finish process
Supply chain and logistics
Toxicity studies
Clinical
Evaluate safety and efficacy
Dose determined
Monitor side effects
Long-term impacts

Workflow of In vivo CAR T Cell Therapy

Solutions for In Vivo CAR-T Cell Therapy Development

mRNA Quality Control

We offer a range of high-quality QC kits designed for comprehensive mRNA quality control, ensuring the integrity and reliability of mRNA in therapeutic and research applications. These kits are optimized for accurate assessment of mRNA purity, integrity, and functionality.

Quantification of antibody density on Ab-LNPs

For in vivo CAR-T, receptor targeting of vector particles is crucial, as it can prevent CAR gene delivery into off-target cells, thus reducing toxicities. T cell biomarker (including CD8, CD3, CD5, CD7 and CD4) antibodies are usually conjugated to LNP or coated on Lentiviral for accurately targeting. Antibody density and activity is a critical quality attribute for the quality, safety, and efficacy of Ab-LNP. We've developed fluorescent-labeled proteins with stable F/P ratio and high activity for quantitative analysis of antibody density on Ab-LNPs.

Ready-to-use due to validation data with various concentration by flow cytometry
Ready-to-use due to validation data with various concentration by flow cytometry

1e5 of Mouse Anti-CD7 antibody coupled beads (5.5 μm) were stained with different concentration of Alexa Fluor 647-Labeled Human CD7 Protein, His Tag (Cat. No. CD7-HA2H4) and negative control protein respectively, AF647 signal was used to evaluate the binding activity (QC tested).

Ready-to-use due to validation data with various concentration by flow cytometry

1e5 of Mouse Anti-CD8 antibody coupled beads (5.5 μm) were stained with different concentration of Alexa Fluor 488-Labeled Human CD8 alpha Protein, His Tag (Cat. No. CDA-HA2H6) and negative control protein respectively, AF488 signal was used to evaluate the binding activity (QC tested).

Ready-to-use due to validation data with various concentration by flow cytometry

1e5 of Mouse Anti-CD4 antibody coupled beads (5.5 μm) were stained with different concentration of Alexa Fluor 647-Labeled Human CD4 Protein, His Tag (Cat. No. CD4-HA2H8) and negative control protein respectively, AF647 signal was used to evaluate the binding activity (QC tested).

High stability
High stability

Alexa Fluor 488-Labeled Human CD7 Protein, His Tag (Cat. No. CD7-HA2H9) is stable at 25℃ for 48 hours, equivalent to store at -70℃ for 2 years and freezing and thawing 3 times without performance reduction.

High batch-to-batch consistency
High batch-to-batch consistency

Binding activity of three different lots of Alexa Fluor 488-Labeled Human CD7 Protein, His Tag against Anti-CD7 CAR-293 cells was evaluated by flow cytometry. The result shows very high batch-to-batch consistency.

No effect on binding activity
No effect on binding activity

Immobilized Alexa Fluor 647-Labeled Human CD7 Protein, His Tag (Cat. No. CD7-HA2H4) at 1 μg/mL (100 μL/well) can bind Anti-CD7 antibody, Mouse IgG1 with a linear range of 0.05-3 ng/mL (Routinely tested). Labeling with fluorescent dyes did not affect their activity.

CAR Detection

We have also developed an extensive collection of CAR target proteins, including fluorescently labeled target antigens and pre-biotinylated proteins, specifically designed for evaluating CAR expression.

ACRO Quality

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