Thalassemia test kit βTHA-RDB

Whole Blood Genomicwhole bloodfor PCR

Beta-mediterranean anemia (β-thalassemia) is a kind of monogenic inheritance hemopathy due to expression imbalance of peptide chain caused by β-globin gene mutation. It is mostly caused by β-globin gene mutation. The commonly seen mutation sites are CD41/42, IVS-Ⅱ-654, -28, CD71/72, etc. Intended Use This kit is used for in vitro qualitative detection of human whole blood genomic DNA sample, which can detect 17 kinds of mutations of β-globin, including 10 kinds of heterozygous mutation (41-42M/N, 654M/N, -28M/N, 71-72M/N, 17M/N, βEM/N, 43M/N, -29M/N, 31M/N and -32M/N) and 7 kinds of mutations which don't distinguish types (IVS-I- 1M, 27/28M, -30M, 14- 15M, CAPM, IntM and IVS-I-5M). General Specification Precision: CV <5% LoD: 2 ng/μL Packing Specifications 25 tests/kit (single test/tube) - 25 tests/kit (non-single test/tube) - 48 tests/lit (non-single test/tube)