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  Invivoscribe provides a full range of standardized CE-marked in vitro diagnostic cGMP products for hematology-oncology, as well as RUO assays, analyte specific reagents (ASRs), and DNA & RNA controls.
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CLINICAL LAB SERVICES
- Clinical Lab Services Overview
  
  The Laboratory for Personalized Molecular Medicine^® (LabPMM^®) at Invivoscribe offer internationally standardized testing of novel and proprietary biomarkers that are critically important for patient care.
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  Accredited & Proven, Registered Medical Device Establishment, Multiple CDx Approvals, CE-marked IVDs, and Marketing Authorization Holder (MAH)
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  Personalized Molecular Medicine^® is use of genomics and patient specific information to identify optimal treatment for each patient.
  EXPLORE PERSONALIZED MEDICINE ⟶
PUBLICATIONS
- Featured Publication
  
  November 17th, 2020
  Routine Evaluation of Minimal Residual Disease in Myeloma Using Next-Generation Sequencing Clonality Testing
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- Latest Publications
  
  April 20th, 2021
  Validation of a Next-Generation Sequencing-based T-Cell Receptor Gamma Gene Rearrangement Diagnostic Assay: Transitioning from Capillary Electrophoresis to Next-Generation Sequencing
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  November 17th, 2020
  Routine Evaluation of Minimal Residual Disease in Myeloma Using Next-Generation Sequencing Clonality Testing
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  Invivoscribe, Inc. (USA)
  
  San Diego, CA, US
  
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  Invivoscribe Therapeutics, Inc. (USA)
  
  San Diego, CA, US
  
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  La Ciotat, France
  
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  Invivoscribe Diagnostic Technologies,(Shanghai) Co.,Ltd.
  
  Shanghai, China
  
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  San Diego, CA, US
  
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  Kawasaki, Japan
  
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  Shanghai, China
  
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Products & Clinical Lab Services

Invivoscribe

PRODUCTS & CLINICAL LAB SERVICES

Cat #: 23100071
BCR/ABL t(9;22) Mix 3b – 6FAM for ABI Fluorescence Detection
BCR/ABL translocations are associated with a variety of hematologic malignancies. The Philadelphia chromosome (Ph1) is a specific chromosomal abnorm...
View Product
Cat #: 11000031
IGH + IGK B-Cell Clonality Assay – ABI Fluorescence Detection
BACKGROUND Rearrangements of the antigen receptor genes occur during ontogeny in B and T lymphocytes. These gene rearrangements generate products th...
View Product
Cat #: 11000041
IGH + IGK B-Cell Clonality Assay MegaKit – ABI Fluorescence Detection
BACKGROUND Rearrangements of the antigen receptor genes occur during ontogeny in B and T lymphocytes. These gene rearrangements generate products th...
View Product
Cat #: 21010061
IGH Framework 1 (FR1) – 6FAM for ABI Fluorescence Detection
Genes encoding immunoglobulin heavy chain (IGH) molecules are assembled from multiple polymorphic gene segments that undergo rearrangement and selecti...
View Product
Cat #: 21010091
IGH Framework 2 (FR2) – 6FAM for ABI Fluorescence Detection
Genes encoding immunoglobulin heavy chain (IGH) molecules are assembled from multiple polymorphic gene segments that undergo rearrangement and selecti...
View Product
Cat #: 21010081
IGH Framework 3 (FR3) – HEX for ABI Fluorescence Detection
Genes encoding immunoglobulin heavy chain (IGH) molecules are assembled from multiple polymorphic gene segments that undergo rearrangement and selecti...
View Product
Cat #: 11010061
IGH Gene Clonality Assay for ABI Fluorescence Detection
BACKGROUND: Rearrangements of the antigen receptor genes occur during ontogeny in B and T lymphocytes. These gene rearrangements generate products t...
View Product
Cat #: 11010081
IGH Gene Clonality Assay MegaKit for ABI Fluorescence Detection
BACKGROUND: Rearrangements of the antigen receptor genes occur during ontogeny in B and T lymphocytes. These gene rearrangements generate products t...
View Product
Cat #: 11010051
IGH Gene Rearrangement Assay for ABI Fluorescence Detection
BACKGROUND: Rearrangements of the antigen receptor genes occur during ontogeny in B and T lymphocytes. These gene rearrangements generate products t...
View Product
Cat #: 11010071
IGH Gene Rearrangement Assay MegaKit for ABI Fluorescence Detection
BACKGROUND: Rearrangements of the antigen receptor genes occur during ontogeny in B and T lymphocytes. These gene rearrangements generate products t...
View Product
Cat #: 51010041
IGH Somatic Hypermutation Assay MegaKit v2.0 for ABI Fluorescence Detection
BACKGROUND Rearrangements of the antigen receptor genes occur during ontogeny in B and T lymphocytes. These gene rearrangements are unique in length...
View Product
Cat #: 51010031
IGH Somatic Hypermutation Assay v2.0 for ABI Fluorescence Detection
BACKGROUND Rearrangements of the antigen receptor genes occur during ontogeny in B and T lymphocytes. These gene rearrangements are unique in length...
View Product
Cat #: 21010011
IGH Tube A – 6FAM for ABI Fluorescence Detection
The immunoglobulin heavy chain (IGH) gene locus on chromosome 14 (14q32.3) includes 46-52 functional and 30 non-functional variable (VH) gene segments...
View Product
Cat #: 21010101
IGH Tube B – 6FAM for ABI Fluorescence Detection
The immunoglobulin heavy chain (IGH) gene locus on chromosome 14 (14q32.3) includes 46-52 functional and 30 non-functional variable (VH) gene segments...
View Product
Cat #: 21010031
IGH Tube C – HEX for ABI Fluorescence Detection
The immunoglobulin heavy chain (IGH) gene locus on chromosome 14 (14q32.3) includes 46-52 functional and 30 non-functional variable (VH) gene segments...
View Product
Cat #: 21010041
IGH Tube D – HEX for ABI Fluorescence Detection
The immunoglobulin heavy chain (IGH) gene locus on chromosome 14 (14q32.3) includes 46-52 functional and 30 non-functional variable (VH) gene segments...
View Product
Cat #: 21010051
IGH Tube E – 6FAM for ABI Fluorescence Detection
The immunoglobulin heavy chain (IGH) gene locus on chromosome 14 (14q32.3) includes 46-52 functional and 30 non-functional variable (VH) gene segments...
View Product
Cat #: 11020021
IGK Gene Clonality Assay for ABI Fluorescence Detection
BACKGROUND Rearrangements of the antigen receptor genes occur during ontogeny in B and T lymphocytes. These gene rearrangements generate products th...
View Product
Cat #: 11020031
IGK Gene Clonality Assay MegaKit for ABI Fluorescence Detection
BACKGROUND Rearrangements of the antigen receptor genes occur during ontogeny in B and T lymphocytes. These gene rearrangements generate products th...
View Product
Cat #: 21020011
IGK Tube A – 6FAM for ABI Fluorescence Detection
The human immunoglobulin kappa (IGK) light chain locus on the short arm of chromosome 2 (2p11.2) spans 1820 kb. It is made up of 76 variable (Vκ) g...
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INVIVOSCRIBE

Invivoscribe, Inc. (USA)

San Diego, CA, US

Invivoscribe Therapeutics, Inc. (USA)

San Diego, CA, US

Invivoscribe, SARL (France)

La Ciotat, France

Invivoscribe Diagnostic Technologies, (Shanghai) Co., Ltd.

Shanghai, China

CLINICAL LAB LOCATIONS

LabPMM, LLC (USA)

San Diego, CA, US

LabPMM, GmbH (Germany)

Munich, Germany

LabPMM, GK (Japan)

Kawasaki, Japan

Invivoscribe Diagnostic Technologies, (Shanghai) Co., Ltd.

Shanghai, China

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© 2018 - | Invivoscribe, Inc. | All Rights Reserved

End User License Agreement

THIS END USER LICENSE AGREEMENT MUST BE ACCEPTED BY AN AUTHORIZED REPRESENTATIVE OF THE END USER OF THIS PRODUCT PRIOR TO USING THE LYMPHOTRACK® DX SOFTWARE(the “Software”). BY USING THE LYMPHOTRACK® DX SOFTWARE, YOU ASSERT THAT YOU ARE AN AUTHORIZED REPRESENTATIVE OF THE END USER WITH AUTHORITY TO ENTER INTO THIS AGREEMENT. PLEASE READ THIS AGREEMENT CAREFULLY. BY USING THE SOFTWARE, YOU ARE AGREEING TO BE BOUND BY THE TERMS OF THIS AGREEMENT. IF YOU DO NOT AGREE TO THE TERMS OF THIS AGREEMENT, PLEASE DISCONTINUE USAGE. IF YOU DO AGREE TO THE TERMS OF THIS AGREEMENT ON BEHALF OF YOURSELF AND/OR THE ENTITY YOU REPRESENT YOU MAY CONTINUE USAGE.

This End User License Agreement (“EULA”) is made and entered into by and between INVIVOSCRIBE, INC, a California corporation. (“Licensor”) and you, as the user of the Software (either you as an individual or a legal entity), the “Licensee” for the licensing and usage of the Licensor’s Software. Licensee acknowledges and agrees that Licensee’s right to use the Software in any manner shall be controlled by this EULA and that such use shall be strictly in accordance with the terms and conditions of this EULA.

1. GRANT OF LICENSE. Licensor grants to Licensee a non-exclusive, non-transferable, limited license, without the right to sublicense, to use the Software and any accompanying written materials and any documents or other content embodying information contained within the Software (collectively, the “Product”) solely for Licensee’s own internal use. Except as agreed in a document signed by Licensor, the Software license granted in the preceding sentence is limited to use with Licensor’s LymphoTrack® Dx Assays purchased from Licensor or from an authorized distributor of Licensor. Licensor reserves all rights not expressly granted to Licensee or to Licensee. The limited license granted by this EULA and Licensee’s payment of the license fee give Licensee the right to use the Product only in accordance with the terms of this EULA. This license is not a sale of the original software or any copy thereof.

2. CONFIDENTIALITY. Licensee agrees that the Product is owned by Licensor and is based on and includes the intellectual property of Licensor, including but not limited to one or more proprietary trade secrets, copyrights, patent applications, and/or granted patents (“Intellectual Property”) of Licensor. Licensee’s possession and use of the Product shall be strictly in accordance with this EULA, and receipt or possession does not convey any rights to divulge, reproduce, or allow others to use the Product outside the terms of this EULA without specific written authorization of Licensor. Licensee agrees not to disclose, publish, translate, release, or distribute copies of the Product or any portion thereof to others outside the terms of this EULA. Licensee may not modify, adapt, translate, reverse engineer, decompile, disassemble, or create derivative works based on the Product or any portion thereof, including any documents or other content produced using the software.

3. OWNERSHIP OF PRODUCT. Title to, ownership of, and all rights and interests in the Product, all copies thereof, and “Intellectual Property” relating thereto, remains at all times vested in Licensor, and this EULA does not grant any ownership rights to Licensee.

4. COPY RESTRICTIONS. The Product is copyrighted. Unauthorized copying or modification of the Product, including but not limited to the Software that has been modified, merged, or included with other software, is expressly forbidden. Licensee may be held legally responsible for any copyright infringement that is caused or incurred by Licensee’s failure to abide by the terms of this EULA.

5. TRANSFER RESTRICTIONS. This Product is licensed to Licensee, and may not be transferred to anyone without the prior written consent of Licensor. In no event may Licensee transfer, assign, rent, lease, sell, or otherwise dispose of the Product, or any portion thereof, on a temporary basis, except as expressly provided herein.

6. TERMINATION. This EULA will be terminated automatically without notice if Licensee fails to comply with any of its provisions.

7. LIMITED WARRANTY. THE PRODUCT, INCLUDING SOFTWARE AND ACCOMPANYING WRITTEN MATERIALS, INCLUDING INSTRUCTIONS FOR USE, ARE PROVIDED “AS IS,” WITHOUT WARRANTY OF ANY KIND, AND LICENSOR DISCLAIMS ALL OTHER WARRANTIES, WHETHER EXPRESS, IMPLIED, OR STATUTORY, INCLUDING ANY IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE, TITLE, NON-INFRINGEMENT AND ANY WARRANTIES ARISING FROM COURSE OF DEALING OR COURSE OF PERFORMANCE REGARDING OR RELATING TO THE SOFTWARE, THE DOCUMENTATION OR ANY MATERIALS FURNISHED OR PROVIDED TO YOU UNDER THIS EULA. LICENSOR DOES NOT WARRANT THAT THE SOFTWARE WILL OPERATE UNINTERRUPTED OR THAT IT WILL BE FREE FROM DEFECTS OR THAT THE SOFTWARE WILL MEET (OR IS DESIGNED TO MEET) YOUR BUSINESS REQUIREMENTS.

8. LIMITED LIABILITY. TO THE MAXIMUM EXTENT PERMITTED BY LAW, IN NO EVENT SHALL LICENSOR BE LIABLE FOR ANY LOST PROFITS OR BUSINESS OPPORTUNITIES, LOSS OF USE, LOSS OFREVENUE, LOSS OF GOODWILL, BUSINESS INTERRUPTION, LOSS OF DATA, OR ANY OTHER INDIRECT, SPECIAL, INCIDENTAL, OR CONSEQUENTIAL DAMAGES UNDER ANY THEORY OF LIABILITY, WHETHER BASED IN CONTRACT, TORT, NEGLIGENCE, PRODUCT LIABILITY, OR OTHERWISE. BECAUSE SOME JURISDICTIONS DO NOT ALLOW THE EXCLUSION OR LIMITATION OF LIABILITY FOR CONSEQUENTIAL OR INCIDENTAL DAMAGES, THE PRECEDING LIMITATION MAY NOT APPLY TO LICENSEE. LICENSOR’S LIABILITY UNDER THIS EULA WILL NOT, IN ANY EVENT, REGARDLESS OF WHETHER THE CLAIM IS BASED IN CONTRACT, TORT, STRICT LIABILITY, OR OTHERWISE, EXCEED THE LICENSE FEES LICENSEE PAID FOR THE SOFTWARE, IF ANY. THE FOREGOING LIMITATIONS SHALL APPLY REGARDLESS OF WHETHER LICENSOR HAS BEEN ADVISED OF THE POSSIBILITY OF SUCH DAMAGES AND REGARDLESS OF WHETHER ANY REMEDY FAILS OF ITS ESSENTIAL PURPOSE.

9. EXCLUSIVE REMEDY. Licensee’s exclusive remedy and Licensor’s entire liability for breach by Licensor of this EULA shall be limited, at Licensor’s sole and exclusive discretion, to: (i) replacement of any defective Software or related Documentation; or (ii) refund of the consideration paid to Licensor for the Software

10. GOVERNING LAW. This EULA shall be governed by the laws of the State of California, irrespective of its conflicts of laws principles, and Licensee consents to jurisdiction by the state and federal courts sitting in the State of California.

11. COMPLETE AGREEMENT. This EULA is the entire agreement between Licensor and Licensee with respect to the specific terms set forth herein concerning license and warranties of the Product and any other included term or obligation. This EULA replaces all prior understandings and agreements, whether written or oral. This EULA may not be modified unless Licensor and Licensee both agree to such modification in writing.

12. SEVERABILITY. If for any reason a court of competent jurisdiction finds any provision or part of any provision of this EULA unenforceable, that part or provision shall be enforced to the maximum extent permitted by law so as to affect the intent of the parties, and the remainder of the EULA shall continue in full force and effect.

©2021 Invivoscribe, Inc. All rights reserved. The trademarks mentioned herein are the property of Invivoscribe, Inc. and/or its affiliates, or (as to the trademarks of others used herein) their respective owners.

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