Thalassemia is a genetic blood disorder caused by when the body does not produce enough hemoglobin. Depending on the damage to the hemoglobin chain, thalassemia is divided into four types: α, β, δβ and δ, with β and α thalassemia being the most common. Currently thalassemia can be well controlled by blood transfusion and chelation therapy. Thalassemia testing is used to determine if a person carries one or more mutations in the gene that produces hemoglobin. There are several tests for thalassemia, including blood tests, DNA analysis, and complete blood counts (CBC).
CD Genomics offers a wide range of thalassemia gDNA standards to assist you in identifying mutations or deletions in the hemoglobin gene that may cause thalassemia, providing valuable information about the cause of thalassemia and the risk of passing it on to offspring.
Genetic testing is the gold standard for the diagnosis of thalassemia. Our technical team has developed thalassemia gDNA standards that can be used throughout the thalassemia genetic testing method to help clients monitor and revise their thalassemia assay protocols, standardize procedures, etc.
Our thalassemia gDNA reference products are derived from human cell lines.
Explore Our Thalassemia gDNA Reference Products:
Cat. No. | Product Name | Brief Description | Inquiry | Basket |
---|---|---|---|---|
TGR001 | CD Thalassemia Wild Type gDNA Reference I | This Thalassemia gDNA Reference is suitable for the whole process of genetic testing methods, which can help monitor and correct your experimental protocols, Referenceize operations, etc. | ||
TGR002 | CD Thalassemia Wild Type gDNA Reference II | This Thalassemia gDNA Reference is suitable for the whole process of genetic testing methods, which can help monitor and correct your experimental protocols, Referenceize operations, etc. | ||
TGR003 | CD Thalassemia Wild Type gDNA Reference III | This Thalassemia gDNA Reference is suitable for the whole process of genetic testing methods, which can help monitor and correct your experimental protocols, Referenceize operations, etc. | ||
TGR004 | CD Thalassemia Alpha Point Mutation gDNA Reference I | This Thalassemia gDNA Reference is suitable for the whole process of genetic testing methods, which can help monitor and correct your experimental protocols, Referenceize operations, etc. | ||
TGR005 | CD Thalassemia Alpha Point Mutation gDNA Reference II | This Thalassemia gDNA Reference is suitable for the whole process of genetic testing methods, which can help monitor and correct your experimental protocols, Referenceize operations, etc. | ||
TGR006 | CD Thalassemia Alpha Point Mutation gDNA Reference III | This Thalassemia gDNA Reference is suitable for the whole process of genetic testing methods, which can help monitor and correct your experimental protocols, Referenceize operations, etc. | ||
TGR007 | CD Thalassemia Alpha Deficiency gDNA Reference I | This Thalassemia gDNA Reference is suitable for the whole process of genetic testing methods, which can help monitor and correct your experimental protocols, Referenceize operations, etc. | ||
TGR008 | CD Thalassemia Alpha Deficiency gDNA Reference II | This Thalassemia gDNA Reference is suitable for the whole process of genetic testing methods, which can help monitor and correct your experimental protocols, Referenceize operations, etc. | ||
TGR009 | CD Thalassemia Alpha Deficiency gDNA Reference III | This Thalassemia gDNA Reference is suitable for the whole process of genetic testing methods, which can help monitor and correct your experimental protocols, Referenceize operations, etc. | ||
TGR010 | CD Thalassemia Alpha Deficiency gDNA Reference Ⅳ | This Thalassemia gDNA Reference is suitable for the whole process of genetic testing methods, which can help monitor and correct your experimental protocols, Referenceize operations, etc. |
Please submit a detailed description of your project. We will provide you with a customized project plan to meet your research requests. You can also send emails directly to for inquiries.
Please fill out the form below: ×