-
,for, Item ID-
- #367016
- Fisher Anatomical #22251050
Hematology Test Kit Pacific Hemostasis® SickleScreen® Sickle Cell Disease / Sickle Cell Trait 30 Tests CLIA Non-Waived
SCREENING KIT, SICKLE CELL (30/PK) FSHSCI
Features
- Thermo Scientific SickleScreen products use a modified Nalbandian procedure that provides fast and accurate results for screening and detecting hereditary sickle cell disease and sickle cell trait. When sickle cell patients are in crisis, their Hb S becomes sickle or cresent shaped and can no longer carry oxygen
- The abnormal cells often break apart and can cause damage to the spleen, kidneys, bone, eyes, lungs and central nervous system
- The procedure is based on the differential solubility of Hemoglobin S (Hb S) and Hemoglobin A (Hb A) in concentrated phosphate solution
- More …
Product Details Email
Product Specifications
| McKesson # | 367016 |
|---|---|
| Manufacturer # | 22251050 |
| Brand | Pacific Hemostasis® SickleScreen® |
| Manufacturer | Fisher Anatomical |
| Country of Origin | Unknown |
| Application | Hematology Test Kit |
| Buy American Act (BAA) Compliant | No |
| CLIA Classification | CLIA Moderate Complexity |
| CLIA Classified | CLIA Non-Waived |
| Contents 1 | 125 mL Bottle of Phosphate Buffer with Dispensing Caps and (30) Pre-filled Reaction Vials |
| For Use With | For Manual, Semi-Automated, and Automated Coagulation Analyzers |
| Number of Tests | 30 Tests |
| Purchase Program Type | Standard Purchase |
| Reading Type | Machine Read / Visual Read |
| Sample Type | Whole Blood Sample |
| Specialty | Hematology |
| Test Format | Tube Format |
| Test Kit Type | Standard |
| Test Method | Modified Nalbandian Procedure |
| Test Name | Sickle Cell Disease / Sickle Cell Trait |
| Test Type | Solubility Test |
| Trade Agreement Act (TAA) Compliant | No |
| UNSPSC Code | 41116120 |
Features
- Thermo Scientific SickleScreen products use a modified Nalbandian procedure that provides fast and accurate results for screening and detecting hereditary sickle cell disease and sickle cell trait. When sickle cell patients are in crisis, their Hb S becomes sickle or cresent shaped and can no longer carry oxygen
- The abnormal cells often break apart and can cause damage to the spleen, kidneys, bone, eyes, lungs and central nervous system
- The procedure is based on the differential solubility of Hemoglobin S (Hb S) and Hemoglobin A (Hb A) in concentrated phosphate solution
More Information
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