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Medical information Clinical review pending

Cytogenetics

Immunohistochemistry ROS1 IHC Test

The Immunohistochemistry ROS1 IHC Test identifies ROS1 gene rearrangements in tumor tissue, guiding targeted cancer therapy decisions. Available across Kenya.

General information only: This page is not a diagnosis or personal medical advice. A qualified clinician should decide whether testing is appropriate and interpret results in context.

Review status: No completed medical review is recorded for this page.

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Counselor guidance included Confidential handling Kenya-wide coordination

At a glance

Plan your test

Sample
Tumor tissue sample (e.g., biopsy, surgical resection). Confirm specific requirements with the laboratory before booking.
Results
Typically 5 to 7 days. Confirm exact turnaround time with the laboratory before booking.
Preparation
No specific patient preparation is required for this test. Ensure the referring physician provides a suitable tumor tissue sample.
Test priceKSh 12,000

Payment: M-Pesa and card options can be confirmed during booking.

Insurance & government schemes

Is this test covered for you?

We help you verify whether the Immunohistochemistry ROS1 IHC Test test can be claimed against your insurer, employer scheme or a Kenyan government health scheme — before you book. Coverage depends on your plan, clinical indication and your provider's rules; final approval always rests with them.

Talk to a claims advisor

Providers & schemes we can help you check

Government & public schemes

SHIF — Social Health Insurance Fund Linda Mama EduAfya NHIF (legacy cards)

Eligibility and benefits follow the current rules of the Social Health Authority (SHA) and applicable government programmes.

Private insurers & employer schemes

Jubilee Health AAR APA Britam CIC Madison Resolution Pioneer Minet Old Mutual GA Life Heritage + other licensed insurers

Names shown for identification only — listing does not imply partnership or guarantee of coverage.

Have these ready when we check

  • Insurer or scheme name & policy / member number
  • A clinician's request / prescription for the test
  • Pre-authorisation letter, if your plan requires one

Free coverage check

Ask us to verify your cover

Send your details and our claims team confirms what documents you need and whether pre-authorisation applies — usually the same working day.

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Used only to process your coverage check — see our Privacy Policy. Verification support is free and does not guarantee your provider will pay.

01

Start with fit

Is this the right test for you?

The best test starts with a clear clinical question. These are common reasons a clinician or family may consider this test.

  • ✓Patients with suspected lung cancer
  • ✓Patients with other malignancies where ROS1 rearrangement is relevant
  • ✓Individuals with risk factors for cancer
  • ✓Patients considering targeted cancer therapies
  • ✓Monitoring treatment response in certain cancers
02

In plain language

What this test helps you understand

Identifies ROS1 protein expression in tumor tissue to guide targeted cancer therapy selection.
The Immunohistochemistry ROS1 IHC Test is an advanced diagnostic procedure used to identify ROS1 gene rearrangements in tumor tissues. This test plays a significant role in the management of cancer, particularly in selecting appropriate targeted therapies for patients. As cancer treatments evolve, understanding the genetic makeup of tumors has become crucial for effective treatment planning.

This test specifically measures the presence of ROS1 protein expression in tumor samples. By analyzing the tumor tissue, healthcare providers can determine if the ROS1 gene is altered, which is essential for guiding treatment options for patients diagnosed with certain types of cancer.

Patients who exhibit symptoms related to lung cancer or other malignancies should consider the Immunohistochemistry ROS1 IHC Test. Key risk factors include a history of smoking, exposure to environmental toxins, family history of cancer, or persistent cough or unexplained weight loss. Consulting with an oncologist can help determine if this test is appropriate based on individual risk factors and symptoms.

Taking the Immunohistochemistry ROS1 IHC Test offers several benefits: it identifies specific genetic mutations that may influence treatment options, helps oncologists tailor therapies to improve patient outcomes, provides valuable information for clinical decision-making, and can lead to earlier and more effective treatment interventions.

Results from the Immunohistochemistry ROS1 IHC Test are typically reported within 5 to 7 days, depending on the complexity of the sample. A positive result indicates the presence of ROS1 rearrangements, which may suggest eligibility for targeted therapies. It is essential to discuss the results with your healthcare provider to understand their implications fully.

We have branches in all major cities in Kenya, making it easy for you to access the Immunohistochemistry ROS1 IHC Test. Additionally, we offer a home sample collection service for your convenience. Book your test today by calling or WhatsApp at +254711564616.
03

Medical review status

Clinical review pending

A completed medical review is not recorded for this page. No clinician has endorsed the information shown here. Please discuss testing decisions with a qualified healthcare professional.

Meet the DNA Labs Kenya medical team →
04

A simple process

What happens next?

You do not have to navigate the test alone. We help you move from question to next step.

1

Speak with us

We check the test and answer your questions before collection.

2

Give your sample

Choose home collection or a coordinated hub visit in Kenya. We explain whether this test uses a cheek swab or blood draw.

3

Understand your report

A counselor helps you understand the result and the next steps.

05

Choose your collection

Home collection or a lab visit

We will explain the sample, preparation, and next steps before anything is collected.

Home collection

Choose a coordinated visit at home or another convenient location. Our team confirms the appointment and sample requirements in advance.

Lab or hub visit

Prefer to visit a coordinated location? We can guide you to the right hub and explain what to expect when you arrive.

Ask about locations →
PreparationNo specific patient preparation is required for this test. Ensure the referring physician provides a suitable tumor tissue sample.
SampleTumor tissue sample (e.g., biopsy, surgical resection). Confirm specific requirements with the laboratory before booking.
MethodologyImmunohistochemistry (IHC) on tissue sections.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects ROS1 protein expression, which correlates with ROS1 gene rearrangements but may not capture all genetic alterations. Results must be interpreted in the context of clinical findings and other diagnostic tests. Confirm with the laboratory before booking.
06

Read your report

What common result terms mean

PositiveA finding was identified. Your clinician or counselor will explain what it means for your care.
NegativeThe specific finding tested for was not identified. It does not rule out every possible cause.
VUSA variant was found, but current evidence is not enough to classify it. Your counselor can explain follow-up.
07

Questions people ask

Frequently asked questions

This test helps identify specific genetic changes (ROS1 rearrangements) in cancer cells to guide treatment decisions, particularly for targeted therapies.
Patients diagnosed with certain types of cancer, especially lung cancer, may need this test to determine if they are eligible for specific treatments.
A tissue sample, usually obtained from a biopsy or surgery, is required for this test.
Results are typically available within 5 to 7 days, but this can vary. Confirm with the laboratory.
A positive result indicates the presence of ROS1 protein expression, suggesting a ROS1 rearrangement. Your doctor will discuss the implications and potential treatment options.
08

Collaboration

Open for partnership with hospitals, clinics, doctors & researchers

Whether you are referring patients, building a research programme or supporting students, we work as an extension of your team — with responsive communication and clear scientific standards.

Hospitals & clinics

Referral pathways, coordinated sample logistics and shared reporting that fits your clinical workflow.

Doctors & specialists

LOINC-coded reports, ACMG-based variant classification and a direct scientific line for complex cases.

Research institutions

Sanger sequencing, NGS panels and custom assays — with project design support, batch pricing and agreed turnaround commitments.

Students & academic projects

Discounted laboratory services for college, master's and PhD research projects — including proposal guidance and cost-effective batch testing.

Explore partnerships
09

Trust & transparency

Sources, standards & how this page is maintained

Standards & references

  • ACMG/AMP technical standards for sequence variant interpretation
  • ClinGen curation and gene–disease validity frameworks where applicable
  • LOINC-coded reporting for interoperable results
  • ISO 9001:2015 quality management; ISO 15189 accreditation in progress

Page provenance

  • Last updated: September 27, 2026
  • Medical review: not yet completed
  • Written for patients & clinicians in Kenya; reviewed periodically against current guidance

Medical disclaimer: this page is general information, not a diagnosis or personal medical advice. Testing decisions and result interpretation should be made with a qualified healthcare professional.

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