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  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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  Lymphoma is a cancer that starts in cells that are part of the body’s immune system. Knowing which type of lymphoma you have is important because it affects your treatment options and your outlook (prognosis).
  
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  Multiple myeloma is a cancer of plasma cells. Normal plasma cells are found in the bone marrow and are an important part of the immune system.
  
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  Routine Evaluation of Minimal Residual Disease in Myeloma Using Next-Generation Sequencing Clonality Testing
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  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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Cat #: K4120331
リューコストラットＣＤｘＦＬＴ３変異検査 (R)
リューコストラットCDx FLT3 変異検査は、日本国内でギルテリチニブフマル酸塩およびキザルチニブ塩酸塩の両方...
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Cat #: 12070111
T-Cell Receptor Gamma Gene Rearrangement Assay MegaKit 2.0
BACKGROUND Invivoscribe’s T-Cell Receptor Gamma Gene Rearrangement Assay 2.0 represents an improved approach to PCR-based clonality testing of T-cel...
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Cat #: 12070051
T-Cell Receptor Gamma Gene Rearrangement Assay for ABI Fluorescence Detection
BACKGROUND Rearrangement of the variable (Vγ) and joining (Jγ) gene segments of the TRG locus results in Vγ-Jγ products of unique length and seque...
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Cat #: 12070101
T-Cell Receptor Gamma Gene Rearrangement Assay 2.0
BACKGROUND Invivoscribe’s T-Cell Receptor Gamma Gene Rearrangement Assay 2.0 represents an improved approach to PCR-based clonality testing of T-cel...
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Cat #: 20960020
Specimen Control Size Ladder – Unlabeled for Gel Detection
Sample quality is critical and therefore it must be verified before the samples are used in molecular assays. Analysis of degraded DNA samples can res...
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Cat #: 20960021
Specimen Control Size Ladder – 6FAM for ABI Fluorescence Detection
Sample quality is critical and therefore it must be verified before the samples are used in molecular assays. Analysis of degraded DNA samples can res...
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Cat #: 40870320
Sensitivity Panel – IVS-0032 Clonal Control RNA
Each tube in this RNA Sensitivity Panel is adjusted to a final concentration of 400 μg/ml with molecular grade water. RNA sensitivity panels are 7 me...
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Cat #: 40870200
Sensitivity Panel – IVS-0020 Clonal Control RNA
Each tube in this RNA Sensitivity Panel is adjusted to a final concentration of 400 μg/ml with molecular grade water. RNA sensitivity panels are 7 me...
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Cat #: 40870150
Sensitivity Panel – IVS-0015 Clonal Control RNA
Each tube in this RNA Sensitivity Panel is adjusted to a final concentration of 400 μg/ml with molecular grade water. RNA sensitivity panels are 7 me...
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Cat #: 40870110
Sensitivity Panel – IVS-0011 Clonal Control RNA
Each tube in this RNA Sensitivity Panel is adjusted to a final concentration of 400 μg/ml with molecular grade water. RNA sensitivity panels are 7 me...
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Cat #: 40870030
Sensitivity Panel – IVS-0003 Clonal Control RNA
Each tube in this RNA Sensitivity Panel is adjusted to a final concentration of 400 μg/ml with molecular grade water. RNA sensitivity panels are 7 me...
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Cat #: S100004
NPM1 MRD Software for Use on Illumina^® MiSeq^TM Platform
The NPM1 MRD Assay for use with the Illumina® MiSeqTM platform was designed to produce sequencing data that can be analyzed using the NPM1 MRD Softwa...
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Cat #: 40880108
LymphoTrack^® T-Cell Low Positive Control
The T-cell LymphoQuant Internal Control and T-cell LymphoTrack Low Positive Control are utilized in controlled MRD studies of TRG and TRB gene rearran...
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Cat #: 75000007
LymphoTrack^® Software – S5/PGM^™
The LymphoTrack® Assays – S5/PGM™ were designed to produce sequencing data that can be analyzed using the LymphoTrack® Software – S5/PGM�...
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Cat #: 75000009
LymphoTrack^® Software – MiSeq^®
The LymphoTrack® Assays – MiSeq® were designed to produce sequencing data that can be analyzed using the LymphoTrack® Software – MiSe...
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Cat #: 75000008
LymphoTrack^® MRD Software
For a Sequence Detected result, the software will report the number of reads and cumulative frequencies of exact sequence matches and similar sequence...
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Cat #: S100003
LymphoTrack^® Enterprise Software
The LymphoTrack Enterprise Software package was designed to enable pipeline automation for high-throughput sequencing laboratories using LymphoTrack A...
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Cat #: 95000007
LymphoTrack^® Dx Software – S5/PGM™
The LymphoTrack Dx Assays – S5/PGM™ were designed to produce sequencing data that can be analyzed using the LymphoTrack Dx Software – S5/PGM...
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Cat #: 95000009
LymphoTrack^® Dx Software – MiSeq^®
The LymphoTrack® Dx Assays were designed to produce sequencing data that can be analyzed using the LymphoTrack Dx Software – MiSeq® package pr...
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Cat #: 92270009
LymphoTrack^® Dx TRG Assay Panel – MiSeq^TM
This LymphoTrack Dx TRG Assay Panel – MiSeq represents a significant improvement over existing clonality assays using fragment analysis as it effic...
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Cat #: 92270019
LymphoTrack^® Dx TRG Assay Kit A – MiSeq^TM
This LymphoTrack TRG Assay – MiSeq represents a significant improvement over existing clonality assays using fragment analysis as it efficiently d...
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Cat #: 92270007
LymphoTrack^® Dx TRG Assay – S5/PGM™
The human T-cell receptor gamma (TRG, previously known as TCRG) gene locus on chromosome 7 (7q14) includes 14 V (variable region) genes (Group I, II, ...
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Cat #: 92250019
LymphoTrack^® Dx TRB Assay Panel – MiSeq^TM
This LymphoTrack TRB Assay – MiSeq represents a significant improvement over existing clonality assays using fragment analysis as it efficiently d...
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Cat #: 92250009
LymphoTrack^® Dx TRB Assay Kit A – MiSeq^TM
This LymphoTrack TRB Assay – MiSeq represents a significant improvement over existing clonality assays using fragment analysis as it efficiently d...
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INVIVOSCRIBE

Invivoscribe, Inc. (USA)

San Diego, CA, US

Invivoscribe, SARL (France)

Marseille, 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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End User License Agreement

CAREFULLY READ THE TERMS OF THIS END USER LICENSE AGREEMENT BETWEEN YOU AND INVIVOSCRIBE, INC., A CALIFORNIA CORPORATION (“LICENSOR”) BEFORE ACCESSING OR USING Invivoscribe Software (THE “PRODUCT”). BY ACCESSING OR USING THE PRODUCT, OR CLICKING BELOW TO ACKNOWLEDGE YOUR ACCEPTANCE OF THE TERMS AND CONDITIONS OF THIS AGREEMENT, YOU, AS THE USER OF THE PRODUCT, IN WHATEVER CAPACITY (EACH AN “AUTHORIZED USER”), AGREE TO THE TERMS OF THIS AGREEMENT. IF YOU DO NOT AGREE TO ALL OF THE TERMS OF THIS AGREEMENT, DO NOT ACCESS OR USE THE PRODUCT, OR CLICK BELOW TO ACKNOWLEDGE YOUR ACCEPTANCE OF THE TERMS AND CONDITIONS OF THIS AGREEMENT. BY USING THE PRODUCT, YOU ASSERT THAT YOU ARE AN AUTHORIZED REPRESENTATIVE OF THE END USER WITH AUTHORITY TO ENTER INTO THIS AGREEMENT.

This End User License Agreement (“Agreement”) is made and entered into by and between INVIVOSCRIBE, INC., a California corporation (“Licensor”) and You (either an individual or a legal entity), the “Licensee,” as defined herein 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 Agreement and that such use shall be strictly in accordance with the terms and conditions of this Agreement.

GRANT OF LICENSE. Licensor grants to Licensee a non-exclusive, non-transferable, limited license, without 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”) only for Licensee’s own 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 Assays purchased from Licensor or from an authorized distributor of Licensor. Licensor reserves all rights not expressly granted to Licensee. The limited license granted by this Agreement and Licensee’s payment of the license fee, if any, give Licensee the right to use the Product only in accordance with the terms of this Agreement. This license is not a sale of the original software or any copy.
CONFIDENTIALITY. Licensee agrees that the Product is based on and includes the intellectual property, including proprietary trade secrets, inventions, copyrights, patent applications, and/or granted patents (“Intellectual Property”) of Licensor, and that Licensor owns all such Intellectual Property. Possession and use of the Product shall be strictly in accordance with this Agreement, and receipt or possession does not convey to Licensee any rights in the Product or the Intellectual Property, or any rights to divulge, reproduce, or allow others to use the Product outside the terms of this Agreement without specific written authorization of Licensor. Licensee agrees not to disclose, copy, publish, translate, release, or distribute copies of the Product or any portion thereof to others outside the terms of this Agreement. Licensee may not modify, adapt, translate, reverse engineer, decompile, disassemble, or create derivative works based on any portion of the Product, including any documents or other content produced using the software.
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SEVERABILITY. If for any reason a court of competent jurisdiction finds any provision or part of any provision of this Agreement unenforceable or contrary to law, such provision or part will be changed and interpreted so as to best accomplish the objectives of the original provision to the fullest extent allowed by law and the remaining provisions of the Agreement shall continue in full force and effect.
EQUITABLE RELIEF. The parties agree that a material breach of this Agreement adversely affecting Licensor’s intellectual property rights in Product may cause irreparable injury to Licensor for which monetary damages would not be an adequate remedy and the non-breaching party shall be entitled to equitable relief (without a requirement to post a bond) in addition to any remedies it may have hereunder or at law.
LEGAL FEES. In any action to enforce one’s rights hereunder, the non-prevailing party shall pay the reasonable fees and expenses of the prevailing party.
ARBITRATION. Any dispute arising out of or relating to this Agreement shall be settled by binding arbitration in accordance with the commercial rules of JAMS (formerly the Judicial Arbitration and Mediation Services) by one arbitrator. Each party shall select one arbitrator, and such two arbitrators shall select a third independent arbitrator, which third arbitrator shall be the sole arbitrator in the matters. Selection of arbitrators shall be made within 30 days after the date of the first notice of demand for arbitration. The results of such arbitration proceedings shall be binding upon the parties hereto, and judgment may entered upon the arbitration award in any court having jurisdiction thereof. The cost of each arbitration proceeding shall be borne equally by the parties. The parties shall pay all of their own expenses of the arbitration, including but not limited to legal fees and costs. The arbitrator shall also award the party that prevails substantially in the arbitration its reasonable attorneys’ fees and costs incurred in connection with the arbitration. All arbitration proceedings shall be held in San Diego, California unless the parties agree otherwise. The arbitrator is empowered to render an award of general compensatory damages and equitable relief (including, without limitation, injunctive relief), but is not empowered to award punitive or presumptive damages. The parties hereto will maintain the substance of any proceedings hereunder in confidence and make disclosures to others only to the extent necessary to properly conduct the proceedings or as otherwise required by law. The parties shall instruct the arbitrator to render his/her decision no later than thirty (30) days after the submission of the dispute. Notwithstanding the foregoing, either party may seek interim injunctive relief from any court of competent jurisdiction.
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©2022 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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