Home - Invivoscribe

Skip to content

2021 CATALOGS
NEWSROOM
CONTACT
LabPMM
MY ACCOUNT
CART

Search for:

PRODUCTS
- Products Overview
  
  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.
  EXPLORE PRODUCTS ⟶
  SEARCH PRODUCT DOCUMENTS & IFUs ⟶
- Next-Generation Sequencing
  CE-IVD
  Illumina®
  Thermo Fisher®
  RUO
  Illumina®
  Thermo Fisher®
  MRD Clonality
- Companion Diagnostics (CDx)
  LeukoStrat® CDx FLT3 Mutation Assay
  CE-IVD
  IVD (US)
  IVD (JP)
- ABI Fluorescence Detection
  CE-IVD
  Clonality
  FLT3
  RUO
  Clonality
  FLT3
  Translocations
- Gel Detection
  CE-IVD
  Clonality
  FLT3
  Translocations
  RUO
  Clonality
  FLT3
  Translocations
- Controls
  Master Mix Controls
  DNA Controls
  RNA Controls
  MRD Controls
- Reagents
  ASRs
  Enzymes
  Hi-Di Formamide
- 2021 Product Catalog
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.
  EXPLORE SERVICES ⟶
- Companion Diagnostic (CDx) Tests
  CDx – USA
  CDx – Germany
  CDx – Japan
- NGS Cancer Panels
  MyAML
  MyMRD
  MyMRD Myeloid
- MFC Panels
  Hematolymphoid Screening Panel
  AML MRD Assay
- MRD NGS Tests
  Clonality
  FLT3 ITD
  NPM1
- Clonality NGS Tests
  SHM
  IGH
  IGK
  TRG
  TRB
DISEASES
- Lymphoid
  Mature B-cell
  Mature T-cell
- Myeloid
  Myelodysplastic Syndromes (MDS)
  Acute Myeloid Leukemia (AML)
  Myeloproliferative Neoplasms (MPNs)
- Hematological Testing Menu
  
  Browse our comprehensive menu of product & testing services.
  EXPLORE MENU ⟶
PARTNERSHIPS
- Partnerships Overview
  
  A proven strategy to accelerate drug approvals
  EXPLORE PARTNERSHIPS ⟶
- Product Development
  
  Design Controls, Bioinformatics Software, Identify & Track, Custom Development, and Complementary MRD Assays
  EXPLORE ⟶
- Manufacturing
  
  cGMP Compliant, CE-marked IVDs & CDx Manufacturing, Assay Development, and Controls & Reagents
  EXPLORE ⟶
- LabPMM®
  
  Clinical Lab Experience, Internationally Standardized, Comprehensive Panels, Complementary MRD Assays, and Worldwide Enrollment
  EXPLORE ⟶
- Global Regulatory Expertise
  
  Accredited & Proven, Registered Medical Device Establishment, Multiple CDx Approvals, CE-marked IVDs, and Marketing Authorization Holder (MAH)
  EXPLORE ⟶
SCIENCE
- Science Overview
  
  We take pride in expanding the science that bridges personalized medicine with quality healthcare.
  EXPLORE OUR SCIENCE ⟶
- Personalized Medicine
  
  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
  VIEW PUBLICATION ⟶
- 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
  VIEW PUBLICATION ⟶
  
  November 17th, 2020
  Routine Evaluation of Minimal Residual Disease in Myeloma Using Next-Generation Sequencing Clonality Testing
  VIEW PUBLICATION ⟶
  
  VIEW ALL PUBLICATIONS ⟶
COMPANY
- Company
  About Us
  Leadership Team
  Board of Directors
  Global Distributors
  Licensure and Certifications
  Search Career Openings
- Invivoscribe Locations
  
  Invivoscribe, Inc. (USA)
  
  San Diego, CA, US
  
  CONTACT US ⟶
  
  Invivoscribe Therapeutics, Inc. (USA)
  
  San Diego, CA, US
  
  CONTACT US ⟶
  
  Invivoscribe, SARL (France)
  
  La Ciotat, France
  
  CONTACT US ⟶
  
  Invivoscribe Diagnostic Technologies,(Shanghai) Co.,Ltd.
  
  Shanghai, China
  
  CONTACT US ⟶
- Clinical Lab Locations
  
  LabPMM, LLC (USA)
  
  San Diego, CA, US
  
  CONTACT US ⟶
  
  LabPMM, GmbH (Germany)
  
  Munich, Germany
  
  CONTACT US ⟶
  
  LabPMM, GK (Japan)
  
  Kawasaki, Japan
  
  CONTACT US ⟶
  
  Invivoscribe Diagnostic Technologies,(Shanghai) Co.,Ltd.
  
  Shanghai, China
  
  CONTACT US ⟶
- Support
  
  Invivoscribe, Inc. (USA)
  
  CONTACT US ⟶
  
  Invivoscribe, SARL (France)
  
  CONTACT US ⟶
  
  Invivoscribe Diagnostic Technologies,(Shanghai) Co.,Ltd.
  
  CONTACT US ⟶
  
  LabPMM, LLC (USA)
  
  CONTACT US ⟶
  
  LabPMM, GmbH (Germany)
  
  CONTACT US ⟶
  
  LabPMM, GK (Japan)
  
  CONTACT US ⟶

SEARCH & FILTER

Territory
- AUS
- European Economic Area
- Mexico and Canada
- Outside North America
- US
Detection
- ABI
- ASR – Undefined
- Capillary Electrophoresis
- Gel
- Ion PGM™
- Ion S5™
- MiSeq®
- NGS
Regulatory Classification
- Analyte Specific Reagent (ASR)
- CAP/CLIA
- CAP/CLIA-validated
- CAP/CLIA-validated LDT
- CE-marked IVD
- Companion Diagnostic
- DAkkS, RiliBAK
- General Purpose Reagent (GPR)
- IVD
- Research Use Only (RUO)
- RUO
- SHM
- To Be Determined
Locus Target
- BCL2-IGH
- BCR-ABL1
- CBFB-MYH11 inv(16)
- Companion Diagnostics
- E2A-PBX1
- FLT3
- FLT3 ITD
- FLT3 ITD MRD Assay
- FLT3 ITD Signal Ratio
- FLT3 TKD
- IGH
- IGH-BCL 1
- IGH-BCL1
- IGH-BCL2
- IGH-CCND1 (BCL1)
- IGK
- IGL
- ITD
- Negative
- NPM1
- PML-RARα
- SHM
- TRB
- TRD
- TRG
Application
- Biomarker Panel
- Clonality
- Coronavirus
- DNA Quality Control
- Gene Panel
- MRD
- Mutation
- Proficiency
- Sensitivity
- Somatic Hypermutation
- Translocation
Product Type
- Assay Kit
- DNA Control
- DNA Sensitivity Panel
- Master Mix
- MRD Control
- Reagent
- Regular Kit (30 Reactions)
- RNA Control
- RNA Dilution Set
- RNA Sensitivity Panel
- Service
- Software
Box Type
- 1-CD
- 1-tube
- 10-tubes
- 100-place box
- 12-place box
- 30-place box
- 6-tubes
- 7-tubes
- LeukoStrat CDx FLT3 Box
Design
- BIOMED
- BIOMED-2
- Genection
- Invivoscribe
- LabPMM
Size
- 1 CD
- 1 Unit
- 1 x 100 uL
- 1 x 1000 uL
- 1 x 1000 µL
- 1 x 1500 uL
- 1 x 1500 µL
- 1 x 1800 µL
- 1 x 200 µL
- 1 x 250 µL
- 1 x 45 uL
- 1 x 50 µL
- 10 x 100 uL
- 1000 µL
- 12 indices per FR region – 5 reactions each
- 12-index Kit (60 reactions)
- 24 indices per FR region – 5 reactions each
- 24-index Kit (120 reactions)
- 6 x 100 uL
- 6 x 50 uL
- 6 x 50 µL
- 7 x 100 uL
- 8 indices per FR region – 5 reactions each
- 8-index Kit (40 reactions)
- MegaKit (300 Reactions)
- MegaKit (300/330 reactions)
- MegaKit (330 reactions)
- Regular Kit (30 Reactions)
- Regular Kit (30/33 reactions)
- Regular Kit (33 reactions)
Reset Filter

SEARCH & FILTER
- Filter Products

HomeMarketing2021-08-30T03:01:12+00:00

Invivoscribe-Shop-FS-1920×275-Background-Image-001

Products & Clinical Lab Services

Invivoscribe

PRODUCTS & CLINICAL LAB SERVICES

Cat #: 13080010
BCL1/J_H Translocation Assay for Gel Detection
BACKGROUND This aberrant BCL1/JH t(11;14) translocation juxtaposes genes of the immunoglobulin heavy chain (IGH) gene on chromosome 14q32 with the cyc...
View Product
Cat #: 23080010
BCL1/J_H Tube – Unlabeled for Gel Detection
The aberrant BCL1/JH t(11;14) translocation juxtaposes genes of the immunoglobulin heavy chain (IGH) gene on chromosome 14q32 with the cyclin D1 gene ...
View Product
Cat #: A3090060
BCL2/J_H 3’Mbr – Unlabeled
This product targets the human BCL2/JH fusion gene. ...
View Product
Cat #: A3090050
BCL2/J_H Mbr – Unlabeled
This product targets the human BCL2/JH fusion gene. ...
View Product
Cat #: A3090070
BCL2/J_H mcr – Unlabeled
This product targets the human BCL2/JH fusion gene. ...
View Product
Cat #: 23090020
BCL2/J_H t(14;18) (mcr) Mix 2b – Unlabeled for Gel Detection
BCL2 translocations are reciprocal chromosome exchanges that place the bcl-2 proto-oncogene, located on chromosome 18, under aberrant transcriptional ...
View Product
Cat #: 13090010
BCL2/J_H t(14;18) Translocation Assay for Gel Detection
BACKGROUND BCL2 translocations are reciprocal chromosome exchanges that place the bcl-2 proto-oncogene, located on chromosome 18, under aberrant trans...
View Product
Cat #: 13090020
BCL2/J_H Translocation Assay for Gel Detection
BACKGROUND BCL2 translocations are reciprocal chromosome exchanges that place the bcl-2 proto-oncogene, located on chromosome 18, under aberrant trans...
View Product
Cat #: 23090050
BCL2/J_H Tube A – Unlabeled for Gel Detection
BCL2 translocations are reciprocal chromosome exchanges that place the bcl-2 proto-oncogene, located on chromosome 18, under aberrant transcriptional ...
View Product
Cat #: 23090060
BCL2/J_H Tube B – Unlabeled for Gel Detection
BCL2 translocations are reciprocal chromosome exchanges that place the bcl-2 proto-oncogene, located on chromosome 18, under aberrant transcriptional ...
View Product
Cat #: 23090070
BCL2/J_H Tube C – Unlabeled for Gel Detection
BCL2 translocations are reciprocal chromosome exchanges that place the bcl-2 proto-oncogene, located on chromosome 18, under aberrant transcriptional ...
View Product
Cat #: 40850310
BCR/ABL b2a2 RNA Dilution Set
Invivoscribe’s BCR/ABL b2a2 RNA Dilution Set consists of RNA that has been extracted from established BCR/ABL b2a2 positive and BCR/ABL negati...
View Product
Cat #: 40850210
BCR/ABL b3a2 RNA Dilution Set
Invivoscribe’s BCR/ABL b3a2 RNA Dilution Set consists of RNA that has been extracted from established BCR/ABL b3a2 positive and BCR/ABL negati...
View Product
Cat #: 40850110
BCR/ABL e1a2 RNA Dilution Set
Invivoscribe’s BCR/ABL e1a2 RNA Dilution Set consists of RNA that has been extracted from established BCR/ABL e1a2 positive and BCR/ABL negati...
View Product
Cat #: 23100010
BCR/ABL t(9;22) Mix 1a – Unlabeled for Gel Detection
BCR/ABL translocations are associated with a variety of hematologic malignancies. The Philadelphia chromosome (Ph1) is a specific chromosomal abnorm...
View Product
Cat #: 23100041
BCR/ABL t(9;22) Mix 1b – HEX 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 #: 23100020
BCR/ABL t(9;22) Mix 2a – Unlabeled for Gel Detection
BCR/ABL translocations are associated with a variety of hematologic malignancies. The Philadelphia chromosome (Ph1) is a specific chromosomal abnorm...
View Product
Cat #: 23100051
BCR/ABL t(9;22) Mix 2b – HEX 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 #: 23100061
BCR/ABL t(9;22) Mix 2c – HEX 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 #: 23100030
BCR/ABL t(9;22) Mix 3a – Unlabeled for Gel Detection
BCR/ABL translocations are associated with a variety of hematologic malignancies. The Philadelphia chromosome (Ph1) is a specific chromosomal abnorm...
View Product

Previous
1
2
3
4
5
6
7
...
17
18
Next

Now Available

Our New Document Search Feature

Need Help Placing an Online Order?

Contact our Customer Service Team

CONTACT CUSTOMER SERVICE ⟶

Now Available

Our New Document Search Feature

Need Help Placing an Online Order?

Contact our Customer Service Team

CONTACT CUSTOMER SERVICE ⟶

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

PRIVACY/TERMS & CONDITIONS

Terms and Conditions
Web Privacy Policy
Privacy Shield Policy
California Consumer Privacy Notice
Licensure and Certifications
Global Distributors

CONNECT

© 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.

CLINICAL LAB SERVICE INQUIRY

Please fill out the form below, and we will respond within 24 hours during a normal business week.
Or call +1 866.623.8105 to speak with an Invivoscribe Representative.

SERVICE*
COMPANY*
POSITION TITLE*
FULL NAME*
PHONE*
EMAIL*
AREA OF INTEREST*
Select all categories that apply.
- CLINICAL TRIALS
- CLINICAL TESTING
- CDX DEVELOPMENT
- MANUFACTURING
- OTHER
MESSAGE
CAPTCHA
Email
This field is for validation purposes and should be left unchanged.

PRODUCTS
CLINICAL LAB SERVICES
DISEASES
PARTNERSHIPS
SCIENCE
- Science Overview
- Personalized Medicine
PUBLICATIONS
- Featured Publication
- Latest Publications
NEWSROOM
COMPANY

LATEST NEWS
Invivoscribe Announces Key Submission in the EU ⟶

CONNECT