ADCC Reporter Bioassay, F Variant

Part Numbers: G9790, G9798, G9302

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FcγRIIIa (F158) 機能を測定する作用機序ベースのバイオアッセイ

  • 細胞培養は不要
  • Fc エフェクター機能における F158 多型の影響を定量

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選択製品のカタログ番号: G9790

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ADCC Reporter Bioassay, F Variant
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Specifically Quantitate the Effect of the FcγIIIa F158 Polymorphism

Fc receptor-mediated antibody-dependent cell-mediated cytotoxicity (ADCC) is an important mechanism of action (MOA) by which antibodies target disease cells for elimination.

The ADCC Reporter Bioassays, F Variant, use NFAT-mediated luciferase activity in effector cells as indicator of ADCC MOA, providing an alternative to traditional primary cell-based assays for measuring the effect of biologics on ADCC activity.

They are accurate, precise and stability-indicating and prequalified according to ICH guidelines, making them suitable for all stages of biologic research and development.

The Pathway

The human FcyRIIIa gene displays a polymorphism in the position coding for amino acid residue 158. This translates to a higher affinity FcyRIIIa variant having a valine at amino acid 158 (V158 and a lower affinity FcyRIIIa variant carrying phenylalanine F158). Killing of target cells is an endpoint of this pathway activation and is used in classic ADCC bioassays, which use donor peripheral blood mononuclear cells (PBMC) or the natural killer (NK) cell subpopulation as effector cells isolated from blood donors with FcyRIIIa VV, VF or FF alleles.

These primary cells can be highly variable in response, are tedious to prepare and can result in high background readings. It is highly challenging to quantitatively evaluate the impact of FcyRIIIa polymorphism by classic in vitro ADCC bioassays. The ADCC Reporter Bioassay, F Variant, overcomes many of these pain points. 

ワークフロー

Standard bioassay workflow with cultured cells
Improved bioassay workflow with thaw-and-use cells

標準化された試薬による改善点

  • 製品に含まれる細胞を融解して使用するだけなので、従来法よりも飛躍的に時間と労力が低減し、バラつきも減少
  • キットは標準化フォーマットとして必要な全ての試薬を供給
  • ハイスループットなワークフローにも容易に適応

The Assay Principle

The Fc Effector Reporter Bioassays use an alternative readout from traditional primary cell based assays: the FcγR and NFAT-mediated activation of luciferase activity in the effector cells. Primary cells are replaced with a Jurkat cell line stably expressing human FcγRIIIa and NFAT-induced luciferase.

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Luminescent Assay Monitors Fc Effector Activity

Following engagement with the Fc region of a relevant antibody bound to a Target Cell, ADCC Bioassay Effector Cells expressing FcγRIIIa F158 will transduce intracellular signals resulting in NFAT-mediated luciferase activity that can be easily quantified.

アッセイパフォーマンスデータ

正確度 (accuracy) と 精度 (precision) はバイオアッセイやバイオロジックス開発において非常に重要です。ADCC Reporter Bioassay は正確度と 精度を兼ね備えたアッセイです(正確度とは標的または参照値に対してどれほど近かったかという度合いであり、精度は再現性の度合いです)。

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ADCC Reporter Bioassay, F Variant, Shows Precision, Accuracy and Linearity

WIL2-S Target Cells

Parameter Results
Accuracy % Expected Relative Potency % Recovery
50 87.7
75 90.4
150 95.1
200 103.1
Repeatability (% CV) 100% (Reference) 3.4
Intermediate Precision (% CV)   6.2
Linearity (r2)   0.997 (50–200% range)
Linearity (y = mx + b)   y = 1.071x – 12.04
 A 50–200% theoretical relative potency series was analyzed in triplicate in three independent experiments performed on three days. The effector-to-target cell ratio (E:T ratio) was 6:1. The ADCC Reporter Bioassay, F Variant, was characterized using ADCC Bioassay Target Cells (WIL2-S). Data were analyzed and relative potencies calculated after parallelism determination using PLA2.1 software from Stegmann Systems GmbH. Data were generated using thaw-and-use cells.

Raji Target Cells

Parameter Results
Accuracy % Expected Relative Potency % Recovery
50 101.3
75 99.2
150 107.8
200 99.3
Repeatability (% CV) 100% (Reference) 5.7
Intermediate Precision (% CV)   7.7
Linearity (r2)   0.993 (50–200% range)
Linearity (y = mx + b)   y = 1.071x + 0.596
 A 50–200% theoretical relative potency series was analyzed in triplicate in three independent experiments performed on three days. The effector-to-target cell ratio (E:T ratio) was 6:1. The ADCC Reporter Bioassay, F Variant, was characterized using ADCC Bioassay Target Cells (Raji). Data were analyzed and relative potencies calculated after parallelism determination using PLA2.1 software from Stegmann Systems GmbH. Data were generated using thaw-and-use cells.

The ADCC Reporter Bioassay is specific for FcγRIIIa-mediated (158F) ADCC

Use the ADCC Reporter Bioassay, F Variant, to:

  • Demonstrate and/or confirm ADCC MOA (or lack thereof)
  • Measure antibody potency and stability
  • Determine the impact of antibody glycosylation and afucosylation on ADCC
  • Screen antibodies
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For experimental details see Technical Manual #TM427.

Product Format

  • ADCC Bioassay, F Variant, is available in 1X and 5X sizes (Cat.# G9790, G9798).
    • Includes ADCC Bioassay Effector Cells, Cell Culture Medium and Assay Reagents.
    • Recommended for routine use with customer-defined antibody and target cells.
  • ADCC Bioassay, F Variant, is also available in CPM format (Cat.# G9302).
    • Includes ADCC Bioassay Effector Cells, F Variant, Propagation Model; these are cryopreserved cells that can be thawed, propagated and banked for long-term use.
    • Use to measure the potency and stability of antibodies and other biologics with Fc domains that specifically bind and activate FcγRIIIa.
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ADCC activity is a major mode of action of therapeutic monoclonal antibodies and is generally determined using a cell-based assay with primary PBMCs. ADCC Reporter Bioassay allows to measure the potency of an antibody without the constraint of PBMC donors’ variability and with a high level of performance. This assay was successfully validated and implemented in our company for batch release testing.

Dr. Fabian Vandermeers, Sr R&D Technical Leader, Quality Assistance S.A.

製品仕様

You are viewing: G9790 Change Configuration

選択製品の構成品内容

Item Part # Size

ADCC Bioassay Effector Cells, F Variant

G979A 1 × 1 vial

Low IgG Serum

G711A 1 × 4ml

RPMI 1640 Medium

G708A 1 × 36ml

Bio-Glo™ Luciferase Assay Buffer

G719A 1 × 10ml

Bio-Glo™ Luciferase Assay Substrate

G720A 1 × 1 vial

分析証明書

Search by lot number

使用制限

Not For Medical Diagnostic Use.

保存条件

Please see the Protocol for detailed storage instructions.

パテントおよび免責条項

NOT FOR MEDICAL DIAGNOSTIC USE. FOR IN VITRO USE ONLY. BY USE OF THIS PRODUCT, RECIPIENT AGREES TO BE BOUND BY THE TERMS OF THIS LIMITED USE STATEMENT. If the recipient is not willing to accept the conditions of this limited use statement, and the product is unused, Promega will accept return of the unused product and provide the recipient with a full refund.
This product may not be further sold or transferred by the recipient and may be used only by the recipient, and then only for (1) research use, (2) drug discovery and development of biologic drugs, (3) quality assurance testing of biologic drugs, and (4) product release assays for biologic drugs. No other commercial use is allowed. "Commercial use” means any and all uses of this product by recipient for monetary or other consideration, including providing a service, information or data to unaffiliated third parties, and resale of this product for any use. Recipient has no right to propagate, modify, derivatize, genetically engineer or otherwise create variations of the Effector Cells or the luciferase gene stably transfected within the Effector Cells. In addition, recipient must use Bio-Glo™ Luciferase Assay System purchased from Promega Corporation for all determinations of luminescence activity of this product, or contact Promega to obtain a license for use of this product with reagents other than Promega’s. PROMEGA MAKES NO REPRESENTATIONS OR WARRANTIES OF ANY KIND, EITHER EXPRESSED OR IMPLIED, INCLUDING AS TO MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE WITH REGARDS TO THIS PRODUCT. The terms of this agreement shall be governed under the laws of the State of Wisconsin, USA.

U.S. Pat. No. 10,077,244 and other patents.

Licensed from Lonza Cologne GmbH under U.S. Pat. Nos. 7,700,357, 8,192,990 and 8,003,389, European Pat. Nos. 1297119, 1522587, 1607484 and 1741778 and other pending and issued patents.

製品仕様

You are viewing: G9798 Change Configuration

選択製品の構成品内容

Item Part # Size

ADCC Bioassay Effector Cells, F Variant

G979A 5 × 1 vial

Low IgG Serum

G711A 5 × 4ml

RPMI 1640 Medium

G708A 5 × 36ml

Bio-Glo™ Luciferase Assay Buffer

G719A 5 × 10ml

Bio-Glo™ Luciferase Assay Substrate

G720A 5 × 1 vial

分析証明書

Search by lot number

使用制限

Not For Medical Diagnostic Use.

保存条件

Please see the Protocol for detailed storage instructions.

パテントおよび免責条項

NOT FOR MEDICAL DIAGNOSTIC USE. FOR IN VITRO USE ONLY. BY USE OF THIS PRODUCT, RECIPIENT AGREES TO BE BOUND BY THE TERMS OF THIS LIMITED USE STATEMENT. If the recipient is not willing to accept the conditions of this limited use statement, and the product is unused, Promega will accept return of the unused product and provide the recipient with a full refund.
This product may not be further sold or transferred by the recipient and may be used only by the recipient, and then only for (1) research use, (2) drug discovery and development of biologic drugs, (3) quality assurance testing of biologic drugs, and (4) product release assays for biologic drugs. No other commercial use is allowed. "Commercial use” means any and all uses of this product by recipient for monetary or other consideration, including providing a service, information or data to unaffiliated third parties, and resale of this product for any use. Recipient has no right to propagate, modify, derivatize, genetically engineer or otherwise create variations of the Effector Cells or the luciferase gene stably transfected within the Effector Cells. In addition, recipient must use Bio-Glo™ Luciferase Assay System purchased from Promega Corporation for all determinations of luminescence activity of this product, or contact Promega to obtain a license for use of this product with reagents other than Promega’s. PROMEGA MAKES NO REPRESENTATIONS OR WARRANTIES OF ANY KIND, EITHER EXPRESSED OR IMPLIED, INCLUDING AS TO MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE WITH REGARDS TO THIS PRODUCT. The terms of this agreement shall be governed under the laws of the State of Wisconsin, USA.

U.S. Pat. No. 10,077,244 and other patents.

Licensed from Lonza Cologne GmbH under U.S. Pat. Nos. 7,700,357, 8,192,990 and 8,003,389, European Pat. Nos. 1297119, 1522587, 1607484 and 1741778 and other pending and issued patents.

製品仕様

You are viewing: G9302 Change Configuration

選択製品の構成品内容

Item Part # Size

ADCC Bioassay Effector Cells, F Variant (CPM)

G930A 2 × 1ml

分析証明書

Search by lot number

使用制限

Not For Medical Diagnostic Use.

保存条件

XX

Please see the Protocol for detailed storage instructions.

パテントおよび免責条項

NOT FOR MEDICAL DIAGNOSTIC USE. FOR IN VITRO USE ONLY. BY USE OF THIS PRODUCT, RECIPIENT AGREES TO BE BOUND BY THE TERMS OF THIS LIMITED USE STATEMENT. If the recipient is not willing to accept the conditions of this limited use statement, and the product is unused, Promega will accept return of the unused product and provide the recipient with a full refund.
This product may not be further sold or transferred by the recipient and may be used only by the recipient, and then only for (1) research use, (2) drug discovery and development of biologic drugs, (3) quality assurance testing of biologic drugs, and (4) product release assays for biologic drugs. No other commercial use is allowed. "Commercial use" means any and all uses of this product by recipient for monetary or other consideration, including providing a service, information or data to unaffiliated third parties, and resale of this product for any use. Recipient has no right to modify, derivatize, genetically engineer or otherwise create variations of the Effector Cells or the luciferase gene stably transfected within the Effector Cells, except that recipient may propagate and store Effector Cells for use in Antibody-Dependent Cell-Mediated Cytotoxicity assays. In addition, recipient must use Bio-Glo™ Luciferase Assay System purchased from Promega Corporation for all determinations of luminescence activity of this product, or contact Promega to obtain a license for use of this product with reagents other than Promega's. PROMEGA MAKES NO REPRESENTATIONS OR WARRANTIES OF ANY KIND, EITHER EXPRESSED OR IMPLIED, INCLUDING AS TO MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE WITH REGARDS TO THIS PRODUCT. The terms of this agreement shall be governed under the laws of the State of Wisconsin, USA.

Licensed from Lonza Cologne GmbH under U.S. Pat. Nos. 7,700,357, 8,192,990 and 8,003,389, European Pat. Nos. 1297119, 1522587, 1607484 and 1741778 and other pending and issued patents.

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