Mouse CTLA4 / CD152 Antibody (clone 9D9)

Mouse IgG2a - For in vivo use

SPECIFICATIONS

Specifications

Target

CTLA-4, CTLA4, CD152

Target species

Mouse

Applications

In vivo studies

Species
Mouse
Isotype
mIgG2a
kappa
Clone
9D9
Tag
Tag-free
Source
CHO cells
Production details
Animal-free
Purification
Protein A
Formulation buffer

Sodium phosphate buffer, saccharose

Preservative
Azide-free
Purity
≥ 95 %
Aggregation

< 5%

Appearance (form)
Lyophilized
Reconstitution buffer
Sterile water (not provided)
Sterility

0.2 µm filtration

Endotoxin

< 1 EU/mg (measurement by kinetic chromogenic LAL assay)

Tested applications

ELISA, in vivo studies

Quality control

Each lot is tested by ELISA.

CONTENTS

Contents

  • Product: 
    Anti-mCTLA4-mIgG2a InvivoFit™
  • Cat code: 
    mctla4-mab10-1
  • Quantity: 
    1 mg

Shipping & Storage

  • Shipping method:  Room temperature
  • Storage:

    • -20 °C
    Stability: -20°C for up to 1 year

    Caution:

    • Avoid repeated freeze-thaw cycles

Details

The cytotoxic T-lymphocyte-associated protein 4 (CTLA-4, also known as CD152) is an inhibitory receptor expressed on activated T lymphocytes. T-cell activation requires two signals. Signal 1 is delivered upon interaction of the T cell receptor (TCR) with antigenic peptides bound to major histocompatibility complex (MHC) molecules on antigen-presenting cells (APCs). Signal 2 is delivered upon interaction of the co-stimulatory receptor CD28 with the B7 family ligands, B7-1 (CD80) and B7-2 (CD86), on APCs.
CTLA-4 is an immune checkpoint molecule upregulated upon T cell activation. It exerts competitive binding to CD28 ligands, thereby preventing T-cell overstimulation. CTLA-4 blockade with monoclonal antibodies (mAbs) has been used to treat patients with metastatic melanoma.

 

In vivo Data

In vivo efficacy of InvivoGen’s Anti-mCTLA4-mIgG2a
In vivo efficacy of InvivoGen’s Anti-mCTLA4-mIgG2a

In vivo efficacy of InvivoGen’s Anti-mCTLA4-mIgG2a

Unlike most immune checkpoint (IC) mAbs on the market, which are produced in hybridomas, InvivoGen’s mouse anti-mouse mAbs are expressed in virus-free CHO cells. This ensures structural stability as well as guaranteeing the highest purity and batch-to-batch consistency; important for mAb efficacy in vivo. 

BALB/c mice were challenged with the murine colorectal carcinoma cell line, CT26. After 8 days, treatment was started with InvivoGen's Anti‑mCTLA4‑mIgG2a (recombinant mAb), Competitor X’s Anti‑mCTLA4 (produced in hybridomas; clone 9D9-mIgG2b), or negative controls (saline only and isotype control mAb). Injections were performed twice a week for 3 weeks (a total of 6 times). After 60 days of monitoring, (A) 7/10 mice were tumor-free in the Competitor X mAb-treated group, compared to (B) 9/9 mice tumor-free in the InvivoGen mAb-treated group. Additionally, no significant differences were observed in the health of the mice, with comparable body weight throughout the study (C). Most notably, after 6 injections, 30%* of the mice in the Competitor X mAb-treated group were euthanized due to excessive tumor volume (endpoint criteria), whereas complete tumor regression was observed in all mice in the InvivoGen mAb-treated group (D). 

In summary, InvivoGen’s optimized Anti‑mCTLA4‑mIgG2a shows increased in vivo efficiency compared to Competitor X’s mAb, which features the commonly used IgG2b isotype, known to display low antitumor activity in vivo.

DOCUMENTS

Documents

Anti-mCTLA4-mIgG2a InvivoFit™

Technical Data Sheet

Validation Data Sheet

Safety Data Sheet

Certificate of analysis

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