Collect

Preferred Bone Marrow aspirate. Acceptable: Leukemic blood, pleural/peritoneal fluid

Specimen Required

Freshly collected – 2.0 mL Bone Marrow Aspirate or 3.0 mL Peripheral Blood. Up to 50.0 mL of body fluids

Specimen Min Vol

1.0 mL of marrow, 2.0 mL blood, 50.0 mL of pleural/peritoneal fluid

Specimen Preparation

Use Sodium Heparin (Green top) preferably. EDTA (purple tube) is also acceptable. Invert several times to mix bone marrow/blood.
Collect body fluids in an aseptic container.
 

Ambient

Preferred. Transport to cytogenetics laboratory as soon as possible, store at room temperature up to 48 hours

Refrigerated

2-8 Celsius degree, If more than 48 hours after collection, and up to 10 days under proper refrigeration

Frozen

Unacceptable

Unacceptable Conditions

Specimens that exceed stated stability, unlabeled/mislabeled/mismatched specimens, specimens submitted in leaking containers/ Samples collected past ten (10) or more days/
Smear slides/Clotted specimen
 

Special Instructions

Order individual or multiple oncology FISH probes if standard FISH panels are not desired.

CPT Codes

88368     
88369     
88377
 

Methodology

Hybridization with commercial DNA probes of cultured cells or cells obtained by direct harvest. 200 interphase nuclei are scored. Two technologists analyze each probe set and all results are expressed as the percent abnormal nuclei.

Performing Location

Cytogenetics Laboratory

Reported STAT

1 - 3 days

Reported Routine

4 - 10 days

Additional Information

Email “CytogeneticsUCI@hs.uci.edu" with questions. 

Time required for testing can vary depending on specimen type and probes ordered.
Please indicate the names of probes needed for testing. 
Contact the Lab at CytogeneticsUCI@hs.uci.edu to add a probe to a current specimen.

This test was developed and its performance characteristics determined by UCI Cytogenetics Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.

Compliance Category: Laboratory Developed Test (LDT)
 

Test set up frequency

Monday - Friday

Reference Interval

As per specific FISH probe validation data

Additional Information

Email “CytogeneticsUCI@hs.uci.edu" with questions. 

Time required for testing can vary depending on specimen type and probes ordered.
Please indicate the names of probes needed for testing. 
Contact the Lab at CytogeneticsUCI@hs.uci.edu to add a probe to a current specimen.

This test was developed and its performance characteristics determined by UCI Cytogenetics Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.

Compliance Category: Laboratory Developed Test (LDT)
 
Collection

Collect

Preferred Bone Marrow aspirate. Acceptable: Leukemic blood, pleural/peritoneal fluid

Specimen Required

Freshly collected – 2.0 mL Bone Marrow Aspirate or 3.0 mL Peripheral Blood. Up to 50.0 mL of body fluids

Specimen Min Vol

1.0 mL of marrow, 2.0 mL blood, 50.0 mL of pleural/peritoneal fluid

Specimen Preparation

Use Sodium Heparin (Green top) preferably. EDTA (purple tube) is also acceptable. Invert several times to mix bone marrow/blood.
Collect body fluids in an aseptic container.
 

Ambient

Preferred. Transport to cytogenetics laboratory as soon as possible, store at room temperature up to 48 hours

Refrigerated

2-8 Celsius degree, If more than 48 hours after collection, and up to 10 days under proper refrigeration

Frozen

Unacceptable

Unacceptable Conditions

Specimens that exceed stated stability, unlabeled/mislabeled/mismatched specimens, specimens submitted in leaking containers/ Samples collected past ten (10) or more days/
Smear slides/Clotted specimen
 

Special Instructions

Order individual or multiple oncology FISH probes if standard FISH panels are not desired.
Test Info

CPT Codes

88368     
88369     
88377
 

Methodology

Hybridization with commercial DNA probes of cultured cells or cells obtained by direct harvest. 200 interphase nuclei are scored. Two technologists analyze each probe set and all results are expressed as the percent abnormal nuclei.

Performing Location

Cytogenetics Laboratory

Reported STAT

1 - 3 days

Reported Routine

4 - 10 days

Additional Information

Email “CytogeneticsUCI@hs.uci.edu" with questions. 

Time required for testing can vary depending on specimen type and probes ordered.
Please indicate the names of probes needed for testing. 
Contact the Lab at CytogeneticsUCI@hs.uci.edu to add a probe to a current specimen.

This test was developed and its performance characteristics determined by UCI Cytogenetics Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.

Compliance Category: Laboratory Developed Test (LDT)
 

Test set up frequency

Monday - Friday
Result Interpretation

Reference Interval

As per specific FISH probe validation data

Additional Information

Email “CytogeneticsUCI@hs.uci.edu" with questions. 

Time required for testing can vary depending on specimen type and probes ordered.
Please indicate the names of probes needed for testing. 
Contact the Lab at CytogeneticsUCI@hs.uci.edu to add a probe to a current specimen.

This test was developed and its performance characteristics determined by UCI Cytogenetics Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.

Compliance Category: Laboratory Developed Test (LDT)
 
NICU/Pediatric Info