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Carcinoma Specific CAR Construction Service

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Are you currently facing challenges in developing effective CAR T cell therapies for solid tumors, struggling with antigen specificity, or overcoming the immunosuppressive tumor microenvironment? Our carcinoma-specific CAR construction service helps you accelerate drug discovery and obtain highly potent, precisely targeted CAR constructs through advanced genetic engineering and comprehensive validation.

Introduction

As a group of cancers, carcinoma usually starts from the skin and spreads to other organs of the body. It accounts for 90% of all cancers, which mostly occur in adults, with the DNA mutation as its main cause. Major subtypes include breast, prostate, colorectal, lung, cervical, melanoma, renal cell carcinoma, and adenocarcinomas. Common symptoms include lumps, skin discoloration, and pain. Although few strategies show effectiveness in carcinoma treatment, immunotherapy has shown great potential as a promising approach to treat carcinoma, such as CAR modified T cells or natural killer (NK) cells. Experts from Creative Biolabs can offer various CAR-T cell or NK cell construction services according to your request.

Fig.1 Modification of CAR-T cells allow them to initiate and amplify the endogenous tumor-specific immune response. (OA Literature) Fig.1 CAR-T cells can be engineered to trigger and enhance the endogenous tumor-specific immune response.1

Carcinoma-Specific CAR Construction at Creative Biolabs

Creative Biolabs' carcinoma-specific CAR construction service provides a comprehensive, end-to-end solution for developing highly effective Chimeric Antigen Receptors tailored to the unique complexities of solid tumors. We deliver meticulously designed and validated CAR constructs, functional CAR-T cells, and detailed data analyses, empowering your preclinical and clinical advancements. Our solutions are specifically engineered to address critical challenges such as tumor antigen heterogeneity, the immunosuppressive tumor microenvironment, and T cell persistence, offering a pathway to more potent and safer immunotherapies for carcinoma.

As a leading and reliable service provider, Creative Biolabs is well known worldwide for its breakthroughs in the CAR production system. Based on targeting carcinoma-specific antigens, our outstanding scientists have constructed diverse CAR-T cells or CAR NK cells targeting these antigens. In addition to these, Creative Biolabs can also customize the CAR product according to your special requirements.

Service Process

The workflow of carcinoma-specific CAR construction service. (Creative Biolabs Original)

Key Advantages

  • Customized CAR Design and Construction: Tailored CAR constructs specifically engineered for your chosen carcinoma antigens and research objectives.
  • Robust Viral Vector Production: High-titer, purified lentiviral or retroviral vectors ensuring efficient and safe gene delivery into T cells.
  • High-Quality CAR-T Cell Manufacturing: Precise T-cell sorting, activation, and transduction protocols to generate functional CAR-T cells suitable for preclinical studies.

FAQs

Q1: What types of carcinomas can your service target?

A1: Creative Biolabs' Carcinoma-Specific CAR Construction Service is highly versatile. We have extensive experience targeting a wide range of carcinomas, including but not limited to renal cell carcinoma, melanoma, lung malignancy, colorectal cancer, prostate cancer, breast cancer, adenocarcinomas, and cervical carcinoma. We can work with both established and novel carcinoma-specific antigens.

Q2: How do you address the immunosuppressive tumor microenvironment (TME) in solid tumors?

A2: We address the challenging TME through advanced CAR designs, including "armored" CARs that are engineered to secrete cytokines or express dominant-negative receptors. These modifications help remodel the TME, enhance T cell persistence, and recruit endogenous immune cells, thereby improving CAR-T cell efficacy in hostile solid tumor environments.

Q3: Can you work with both human and mouse T cells for CAR construction?

A3: Yes, our service is equipped to handle both human and mouse T cells. We utilize appropriate viral vectors (lentiviral for human T cells and retroviral for mouse T cells) and optimized protocols for T-cell sorting, activation, and transduction to ensure successful CAR expression and functionality in both species.

Why Choose Us?

At Creative Biolabs, we are committed to accelerating your journey from scientific concept to therapeutic reality in carcinoma treatment. Our carcinoma-specific CAR construction service combines unparalleled scientific expertise with cutting-edge technology, delivering precise, potent, and safe CAR constructs designed to overcome the unique challenges of solid tumors. Partner with us to transform your research into groundbreaking cancer immunotherapies.

Customer Reviews

"The 4th-generation armored CARs constructed by Creative Biolabs have greatly facilitated our studies on T cell persistence in the harsh tumor microenvironment. We observed remarkably sustained anti-tumor activity, which was a significant improvement compared to our previous constructs." - 2025, Prof. JS Pr

"Creative Biolabs' comprehensive workflow, from scFv selection to final CAR-T cell validation, has streamlined our research process. Their detailed quality control and consistent deliverables have been invaluable in accelerating our preclinical development." - 2025, Dr. Sh Kr

How to Contact Us

Based on a great number of experiments, we are confident our first-class CAR products can greatly accelerate your project process. Please feel free to contact us at any time.

Products against Sarcoma-specific antigens

Associated malignancy Target antigen Receptor type Product
Renal cell carcinoma (RCC) Carbonic anhydrase IX (CAIX) scFv-CD28-41BB-CD3ζ CAR-MZ204
CSPG4 scFv-CD28-CD3ζ CAR-LC134
G250 epitope iRGD-scFv-CD28-41BB-CD3ζ CAR-LC371
VEGFR-2 scFv-CD28-41BB-CD3ζ CAR-LC132
scFv-CD28-CD3ζ CAR-LC133
Melanoma EGFR VHH-CD28-41BB-CD3ζ XS-0323-LX9
scFv-CD28-CD3ζ CAR-LC098
scFv-CD28-41BB-CD3ζ CAR-LC100
Trop2 scFv-CD28-41BB-CD3ζ CAR-LC190
PD-L1 PD1-41BB-CD3ζ CAR-LC282
Cs-1 scFv (SLAMF7)-CD28-41BB-CD3ζ/scFv (FN)-cMYCmu CAR-LC365
BCMA scFv-CD28-41BB-CD3ζ CAR-T-3-L335-2BZ
CS1 scFv-CD28-OX40-CD3ζ CAR-NK-3-M329-2XZ
CSH1 scFv-CD28-41BB-CD3ζ CAR-T-3-L349-2BZ
HMW-MAA scFv-CD28-41BB-CD3ζ CAR-T-3-M318-2BZ
NY-ESO-1 scFv-CD28-41BB-CD3ζ CAR-T-3-M323-2BZ
GD3 scFv-CD28-41BB-CD3ζ CAR-T-3-M317-2BZ
MART-1(DMF5) scFv-CD28-41BB-CD3ζ CAR-T-3-M310-2BZ
CD56 scFv-CD28-41BB-CD3ζ CAR-T-3-M312-2BZ
gp100 VHH-41BB-CD3ζ CAR-T-2-M552-BZ
Lung malignancy Mesothelin scFv-CD28-41BB-CD3ζ CAR-LC054
7H-YB-Fluc-EF1a-scFv-41BB-CD3ζ XS-0822-YF8720
scFv-CD28-CD3ζ CAR-LC024
ALK scFv-CD28-41BB-CD3ζ CAR-LC103
Fibroblast activation protein (FAP) scFv-41BB-CD3ζ CAR-LC224
CD87 scFv-41BB-CD3ζ-IL12 CAR-LC265
Tissue factor Protein-41BB-CD3ζ CAR-LC288
TF scFv-CD28-OX40-CD3ζ CAR-T-3-L406-2XZ
Colorectal cancer CEA scFv-CD28-41BB-CD3ζ CAR-T-3-M314-2BZ
EGP-2 scFv-CD28-41BB-CD3ζ CAR-T-3-M316-2BZ
TAG-72 scFv-CD28-41BB-CD3ζ CAR-T-3-M325-2BZ
CD276 scFv-CD28-CD3ζ CAR-LC162
EpCAM scFv-CD28-41BB-CD3ζ CAR-LC181
HLA-A2-WT1DB126 scFv-CD28-FcγR1γ CAR-LC266
Prostate cancer PSMA 7H-YB-IL15 SA-EF1a-scFv-CD28-CD3ζ XS-0822-YF9698
PSCA scFv-CD28-CD3ζ CAR-MZ157
Breast cancer CD8 scFv-41BB-CD3ζ-IL12 CAR-LC265
ErbB2 scFv-CD28-41BB-CD3ζ CAR-T-3-L337-2BZ
MUC1 scFv-CD28-41BB-CD3ζ CAR-T-3-M322-2BZ
TEM8 scFv-CD28-41BB-CD3ζ CAR-T-3-L343-2BZ
SSEA4 scFv-41BB-CD3ζ CAR-LC001
CD33 scFv-CD28-CD3ζ CAR-LC155
HER2 scFv-41BB-CD3ζ CAR-LC172
NY-BR-1 scFv-CD28-41BB-CD3ζ CAR-LC220
CD44 scFv-CD28-CD3ζ CAR-LC226
CD47 scFv (CD47)-CD28-41BB-CD3ζ/scFv (TAZ)-TET2 CAR-LC364

Reference

  1. Wei, Jianshu et al. “Target selection for CAR-T therapy.” Journal of hematology & oncology vol. 12,1 62. 20 Jun. 2019, https://doi.org/10.1186/s13045-019-0758-x. Distributed under Open Access License CC BY 4.0, without modification.
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