STEMOD™ CPVT1 Disease Model (RYR2, p.F2483I (c.7447T>A))

  • Check with publisher
  • Published date: January 26, 2021
    • United States
STEMOD™ CPVT1 Disease Model (RYR2, p.F2483I (c.7447T>A))
STEMOD™ CPVT1 Disease Model (RYR2, p.F2483I (c.7447T>A))

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited life-threatening arrhythmia leading to syncope and sudden cardiac death at a young age. This disease cell model belongs to CPVT1, an autosomal dominant mutations (p.F2483I, also called c.7447T>A) occur in the RYR2 gene. Generating pluripotent stem cells from dermal fibroblasts, then differentiate into cardiac myocytes. This disease cell model provides a platform to explore disease mechanisms in human genetic cardiac disorders.https://www.creative-biolabs.com/stem-cell-therapy/cpvt1-disease-model-ryr2-p-f2483i-c-7447t-a-41.htm

Result 0 votes
Jerry Carter
1 votes

Useful information

  • Avoid scams by acting locally or paying with PayPal
  • Never pay with Western Union, Moneygram or other anonymous payment services
  • Don't buy or sell outside of your country. Don't accept cashier cheques from outside your country
  • This site is never involved in any transaction, and does not handle payments, shipping, guarantee transactions, provide escrow services, or offer "buyer protection" or "seller certification"

Related listings

  • STEMOD™ CPVT1 Disease Model (RYR2, R420Q (c.1378G>A))

    STEMOD™ CPVT1 Disease Model (RYR2, R420Q (c.1378G>A))

    Cell Biology & Microbiology (United States ) January 26, 2021 Check with publisher

    Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited life-threatening arrhythmia leading to syncope and sudden cardiac death at a young age. This disease cell model belongs to CPVT1, an autosomal dominant mutations (R420Q, als...

  • STEMOD™ CPVT1 Disease Model (RYR2, Q2311D (c.6933G>C))

    STEMOD™ CPVT1 Disease Model (RYR2, Q2311D (c.6933G>C))

    Cell Biology & Microbiology (United States ) January 26, 2021 Check with publisher

    Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited life-threatening arrhythmia leading to syncope and sudden cardiac death at a young age. This disease cell model belongs to CPVT1, an autosomal dominant mutations (Q2311D, al...

  • STEMOD™ CPVT1 Disease Model (RYR2, p.I4587V (c.13759A>G))

    STEMOD™ CPVT1 Disease Model (RYR2, p.I4587V (c.13759A>G))

    Cell Biology & Microbiology (United States ) January 26, 2021 Check with publisher

    Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited life-threatening arrhythmia leading to syncope and sudden cardiac death at a young age. This disease cell model belongs to CPVT1, an autosomal dominant mutations (p.I4587V, ...