1 | ![]() CE IVD only available in certain countries. All other countries research use only! Please contact your local dealer for more information. |
1 | ![]() CE IVD only available in certain countries. All other countries research use only! Please contact your local dealer for more information. |
1 | ![]() CE IVD only available in certain countries. All other countries research use only! Please contact your local dealer for more information. |
1 | ![]() CE IVD only available in certain countries. All other countries research use only! Please contact your local dealer for more information. |
The ZytoFast human Ig-kappa/Ig-lambda Probe (PF22) is intended to be used for the qualitative detection of human Ig-kappa and Ig-lambda light chain mRNA in formalin-fixed, paraffin-embedded specimens, such as multiple myeloma, by chromogenic in situ hybridization (CISH). The probe is intended to be used in combination with the ZytoFast PLUS CISH Implementation Kit HRP-DAB (Prod. No. T 1063-40). The product is intended for professional use only. All tests using the product should be performed in a certified, licensed anatomic pathology laboratory under the supervision of a pathologist/human geneticist by qualified personnel. The probe is intended to be used as an aid to the differential diagnosis of multiple myeloma and therapeutic measures should not be initiated based on the test result alone.
Prod. No.: | Tests¹ (Volume): | Registration Status²: | ||
---|---|---|---|---|
T-1017-400 |
|
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1 | Using 10 μl probe solution per test. |
2 | ![]() CE IVD only available in certain countries. All other countries research use only! Please contact your local dealer for more information. |
The ZytoFast human Ig-kappa/Ig-lambda CISH Kit is intended to be used for the qualitative detection of human Ig-kappa and Ig-lambda light chain mRNA in formalin-fixed, paraffin-embedded specimens, such as multiple myeloma, by chromogenic in situ hybridization (CISH). The product is intended for professional use only. All tests using the product should be performed in a certified, licensed anatomic pathology laboratory under the supervision of a pathologist/human geneticist by qualified personnel. The product is intended to be used as an aid to the differential diagnosis of multiple myeloma and therapeutic measures should not be initiated based on the test result alone.
Prod. No.: | Tests¹: | Registration Status²: |
---|---|---|
T-1005-40 | 40 | ![]() |
|
1 | Using 10 μl probe solution per test. |
2 | ![]() CE IVD only available in certain countries. All other countries research use only! Please contact your local dealer for more information. |
Prod. No.: | Tests¹ (Volume): | Registration Status: | ||
---|---|---|---|---|
T-1053-100 |
|
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1 | Using 10 μl probe solution per test. |