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MLPA Assays for Hereditary Blood Disorders

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MLPA Assays for Hereditary Blood Disorders

MLPA Assays are useful in finding out those who have hereditary blood disorders.

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Features & Benefits

Simultaneous detection of copy number, methylation and select known point mutations.
Low input: Requires only 50 ng of DNA.
Time-efficient: Results available within 24 hours.
Short hands-on time
Cost-effective

Product Details

MLPA Assays are useful in finding out those who have hereditary blood disorders and blood cancers including:

Thalassemia (Alpha, Beta)

Fanconi Anemia

Clotting Factor Deficiencies (V, IX, X, XI)

Von Willebrand Disease

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