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Amoydx Genomics Redefines The Boundaries Of Fungal Genomics Equipment & Supplies Near Lithuania

4 equipment items found
In LithuaniaAvailable In LithuaniaNear Lithuania

AmoyDx - Pan Lung Cancer PCR Panel

AmoyDx - Pan Lung Cancer PCR Panel

Manufactured by:Amoy Diagnostics Co., Ltd.   based inXiamen, CHINA
Lung cancer is one of the most common malignant tumor, and 80~85% of lung cancers are non-small cell lung cancer (NSCLC). There are many driver mutations in NSCLC. The frequency of mutations in NSCLC for EGFR, HER2, KRAS and BRAF genes are respectively 10-50%, 1-4%, 5-25% and 1-2%. About 3-7%, 1%, 1%, 0.12%, 0.02%, 0.08% of NSCLC patients have gene fusions in ALK, ROS1, RET, NTRK1, NTRK2 and ...
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AmoyDx - Model PIK3CA - Mutation Detection Kit

AmoyDx - Model PIK3CA - Mutation Detection Kit

Manufactured by:Amoy Diagnostics Co., Ltd.   based inXiamen, CHINA
The phosphoinositide-3 -kinase catalytic alpha (PIK3CA) gene produces the p110 alpha (pl 10a) protein, which is one subunit of an enzyme called phosphatidylinositol 3-kinase (PI3K). PI3K plays a key role ofPI3K/Akt signaling pathway in numerous cellular processes critical for cancer progression, including metabolism, growth, survival, and motility. Somatic mutations in the PIK3CA gene are found ...
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AmoyDx - Multi-Gene Mutations Detection Kit

AmoyDx - Multi-Gene Mutations Detection Kit

Manufactured by:Amoy Diagnostics Co., Ltd.   based inXiamen, CHINA
Lung cancer is one of the most common malignant tumor, and 80~85% of lung cancers are non-small cell lung cancer (NSCLC). There are many driver mutations in NSCLC. The frequency of mutations in patients with NSCLC for the EGFR gene is 10~35%, for KRAS 15?25%, for BRAF1-4%, for NRAS is 1%, for HER2 2-4%, and for PIK3CA 1-3%. About 3-7% of NSCLC patients have gene fusion in ALK, 2% in ROS1, and 1% ...
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AmoyDx - Handle HRR NGS Panel

AmoyDx - Handle HRR NGS Panel

Manufactured by:Amoy Diagnostics Co., Ltd.   based inXiamen, CHINA
The Homologous Recombination Repair (HRR) pathway plays an important role in double strand break, which is the major cause of cancer development. It has been demonstrated that loss of function of HRR genes (e.g. BRCA1, BRCA2, PALB2) and homologous recombination deficiency (HRD) will cause a higher risk of developing cancer, and patients with HRR gene mutations showed higher response to PARPi and ...
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