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Lab Test

IHC PDL-1 (SP263-FDA approved clone)

The IHC PDL-1 (SP263-FDA approved clone) test is a crucial diagnostic and management tool, primarily used in the field of oncology. It aids in the detection of programmed death-ligand 1 (PD-L1) in tissue samples, contributing to personalized treatment strategies for certain types of cancers.


  • Test NameIHC PDL-1 (SP263-FDA approved clone)
  • Sample TypeTissue
  • Preparations RequiredNo specific preparation or fasting is required before this test.
  • Report Time4 days

What is the IHC PDL-1 (SP263-FDA approved clone) test?

The IHC PDL-1 (SP263-FDA approved clone) test is a pathology test that identifies the presence of programmed death-ligand 1 (PD-L1) in a tissue sample. The expression of PD-L1 can greatly impact the treatment strategy for diseases such as lung cancer and melanoma.

How is the IHC PDL-1 (SP263-FDA approved clone) test performed?

This test is performed on a tissue biopsy sample. The sample is treated with a specific antibody, SP263, which binds to PD-L1 if it is present in the tissue. This interaction can be visualized under a microscope.

Home Sample Collection Process

1
Book your convenient slot
Book your convenient slot
2
Sample Collection by Phlebotomist
Sample Collection by Phlebotomist
3
Reporting of the sample at lab
Reporting of the sample at lab
4
Download Reports
Download Reports
Frequently Asked Questions

No, fasting is not required before this test.

No specific preparations are needed for this test.

Your healthcare provider might recommend the IHC PDL-1 (SP263-FDA approved clone) test if they suspect a disease that can be diagnosed or managed through PD-L1 detection, such as certain types of cancer.

Test results are usually reported as positive or negative for PD-L1 expression. A positive result means PD-L1 was detected in the tissue sample, which can influence treatment options. A negative result indicates PD-L1 was not detected. The interpretation of these results should be discussed with your healthcare provider.

The frequency of this test is determined by your healthcare provider based on your health condition. It's typically ordered when there's clinical suspicion of a disease that can be diagnosed or managed using PD-L1 detection.

There are no specific precautions necessary for the IHC PDL-1 (SP263-FDA approved clone) test. However, it's always advisable to communicate any allergies or medications you're taking to your healthcare provider, as these could potentially impact the biopsy procedure.

While it's rare, the IHC PDL-1 (SP263-FDA approved clone) test results could be influenced by technical errors during the biopsy or testing procedure.

A positive test result indicates the presence of PD-L1 in your tissue sample. In such a case, discuss the results with the healthcare provider who ordered the test. They may refer you to a specialist, such as an oncologist, for further evaluation and treatment planning.

Yes, the IHC PDL-1 (SP263-FDA approved clone) test can be used for both diagnosis and monitoring of diseases. The test provides critical information about the presence or absence of PD-L1, which can help guide treatment strategies.

Yes, the IHC PDL-1 (SP263-FDA approved clone) test can be performed on individuals of all ages, including children. The necessity and appropriateness of this test are determined based on your healthcare provider's clinical judgment.

While the IHC PDL-1 (SP263-FDA approved clone) test itself poses minimal risk, the biopsy procedure used to obtain the tissue sample can carry some risks, including infection, bleeding, and an adverse reaction to anesthesia.

While uncommon, it is possible to receive false positive or negative results from the IHC PDL-1 (SP263- FDA approved clone) test due to technical errors during the testing process. Always discuss your results with your healthcare provider to gain a comprehensive understanding.

The decision to conduct the IHC PDL-1 (SP263-FDA approved clone) test during pregnancy depends on the potential benefits and risks, which should be discussed with your healthcare provider.

The SP263 clone is a specific type of antibody that is used in the IHC PD-L1 test. It has been approved by the FDA for its ability to reliably detect PD-L1 protein expression in tissue samples, aiding in the diagnosis and management of certain cancers.

The type of tissue sample required for the IHC PDL-1 (SP263-FDA approved clone) test depends on the suspected location of disease or abnormality. The sample is usually obtained through a biopsy procedure.

A positive IHC PDL-1 (SP263-FDA approved clone) result means that PD-L1 was detected in the tissue sample. This can suggest certain diseases or conditions, but the interpretation depends on the specific type of disease being investigated and other clinical findings.

There are no known medications that directly interfere with the IHC PDL-1 (SP263-FDA approved clone) test. However, it's always important to discuss all the medications and supplements you're currently taking with your healthcare provider before the test.

The IHC PDL-1 (SP263-FDA approved clone) test is a reliable tool when used in conjunction with other tests and clinical findings. However, no single test should be used as the sole basis for diagnosis. Your healthcare provider will consider these test results along with other diagnostic information.

Understanding the role of PD-L1 expression can be crucial for devising effective therapeutic strategies, especially in the realm of cancer treatment. While the IHC PDL-1 (SP263-FDA approved clone) test provides valuable insights, it is important to discuss your results in depth with your healthcare provider. Always remember that every test is just a piece of the larger health puzzle and should be considered within the context of your overall health and other diagnostic findings.

IHC PDL-1 (SP263-FDA approved clone)
₹ 10500
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