Thalassemia is one of the most comm< >≥on and harmful single-gene genet÷$ic diseases in the world, anemiaπαΩ or pathological state caused by t★ Ω↓he lack or deficiency of one or more gloδ₽§₹bgenin strains in hemoglobin due to genetic beg>✘₩loper gene defects. →₩↓δName and classify the type and degree ofπφ→ glober chain deficiency. Accord↓σ ing to the severity of the disλ★™ease, divided into hσ✔eavy, intermediate, light t✘¶≤σhree types, heavy: 3-6 &×<;months after birth syφ♠ mptoms, often die in childhood;
The dis'₽™εease is widely distributed in∑★ many parts of the world, b♥γπlack areas of the United States, So♥λ≠utheast Asia, the Indian sub &continent and southern China: Guangdonλ™g, Guangxi, Yunnan, Hainan and other places foΩ↔∑♣r high-risk areas, the popu×™&∑lation carrying rate☆¶±γ of up to 24%. At least 350&♠nbsp;million people worldwide car±'λλry the terrestrial poverty gene.
Comprehensive coveraσ÷♦≈ge: more comprehensive coverage ±εof the incidence site detection, for each reg'≈δ∞ion to carry higher gene mutant type₽≥₽₽ supplement, is currently ε ↑a hot gene selection more comprehensive CF≤∏DA registered products, greatly redδ£ucing the risk of missed dete• ction;
High accuracy: detection of known missing types of samples, thβαe results show the co₩✘εrresponding missing type, accuracy is more than☆∏₩ 99%;
High specificity: detection of non-poor huma↓≥n genome DNA samples, specifictocoming more th ¥γ$an 99%;
Technology reliability: technology platform after many →↓ years of clinical and the vast numb≈↑er of hospitals recognized and verified;
Applicability: The conditions of use are ★γ↔<simple and can be carr♥↕ied out in a normal P♣®ε<CR laboratory.
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Product name |
Missing alpha-thalassemia gene tσαest kit |
Non-missing alpha-thala≈≤ssemia gene testkit |
Beta-thalassemia gene mutation test kit |
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Detection method |
Gap-PCR Law |
PCR-reverse point hybridizati§¶δon |
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Sample requirements |
Anticoagulant whole blood or genomic DN÷≠"A |
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Application instruments |
Gene amplification instrument, ♣₽&€electrophoresis |
Gene amplification instrum©Ω∑ent, molecular hybridizer |
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Packaging specifications |
25 tests/kit |
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High accuracy |
Positive and negative <♦compliance rates are ÷®↕up to 100% |
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High sensitivity |
Stable detection of genomic DNA sample ←s with a concentratio ™n of 2 ng/sL |
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Precision |
In-batch and inter-batch pr✔§®oducts using standard•λ genomic DNA testing for precision reference conce₹×>♥ntrations of 10ng/μL |
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Easy to operate time-saving |
After amplification, you can produce results&±€δ☆nbsp; with simple electrophoresis |
Both can be used for PCR, hybrid, color display at the same time |
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Repeatability |
100% consistency |
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Causes of thalassemia；
Thalassaemia risk assΩ☆essment of childcare before preπ≈λgnancy；
Blocking of children with thalassaemia during pΩ¶®nancy；
High-risk groups, newborn screening.
Date:2020-03-26
Date:2020-03-30
Date:2020-03-17
Date:2020-03-11
Date:2020-03-03
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