Fully-Automated
Semi-Automated
Radiology
Point of Care
Stay ahead of the curve with the accurate detection of the six most common mutations in the β-globin gene.
Gain unparalleled convenience by detecting FXS and differentiating normal, pre-mutation, and full mutation genotypes.
Upgrade your lab's performance with advanced PCR technology that assists in the diagnosis of β-Thalassemia.
Simplify your services with separate extraction reagents for blood samples & PCR amplification ones specific to the common mutations.
Detects common mutations like codon 8/9 (+G), IVS 1-1 (G>T), 619 bp del, IVS 1-5 (G>C), codon 41/42, & codon 15 (G>A)
It is intended for carrier testing in adults of reproductive age & newborn screening
Used as a confirmatory diagnostic test in newborns and children.
| Catalog Number | Reaction Size | Enquire |
|---|---|---|
| 1070A025 | 25 | Enquire Now |
| 1070A050 | 50 | Enquire Now |
| 1070A100 | 100 | Enquire Now |
| Catalog Number | Reaction Size | Enquire |
|---|---|---|
| 1070C025 | 25 | Enquire Now |
| 1070C050 | 50 | Enquire Now |
| 1070C100 | 100 | Enquire Now |
5th Floor, Amar Paradigm, Survey No – 110/11/3, Baner Rd, Pune – 411045. Maharashtra, India.
