AccurEdit Therapeutics (Suzhou) Co., Ltd. (“AccurEdit”) announced that its self-developed product ART001 targeting transthyretin amyloidosis (ATTR) has recently received IND clearance from the U.S. FDA, making it the first non-viral vector-based in vivo gene editing drug from China to obtain…
I want to order some gene edited mice model. But I am curious about the different between C57BL/6J and 6N, are they the same or different? Actually, B6N are 99% identical to B6J, and they can be used for most…
VeloGene Biotechnology The Living Test Tube skip render: ucaddon_list_marquee The Living Test Tube: Mouse Models, ESC Technology, and the TurboMice™ Revolution 1. Introduction: What is a Mouse Model? In modern biomedical research, understanding human disease requires more than test tubes…
What Is Congenital Thrombotic Thrombocytopenic Purpura? Congenital Thrombotic Thrombocytopenic Purpura (cTTP), also named congenital ADAMTS13 deficiency, is an extremely rare inherited hematologic disease. As one of the two major subtypes of thrombotic thrombocytopenic purpura (TTP), it differs from immune-mediated acquired…
Why VeloGene? TurboMice™ – Rapid Mouse Model Technology Mono Chromosome Multipoint Gene Editing VeloGene TurboMice™ Tetraploid Complementation Technology: Overcoming Multi-Loci Editing on the Same Chromosome, Delivering “Clone-Grade” Mice Directly at the F0 Generation In the construction of genetically engineered animal…
What Is Isovaleric Acidemia? Isovaleric Acidemia (IVA) is a rare autosomal recessive inborn organic acid metabolic disorder caused by pathogenic variants in the IVD gene encoding isovaleryl-CoA dehydrogenase. Gene defects block leucine catabolism, leading to massive systemic accumulation of toxic…
Six years have quietly passed since our core scientific team completed a milestone technological leap in early 2020. Today, as global drug discovery pipelines accelerate at an unprecedented pace, the biotech industry increasingly demands smarter, faster, and more predictive preclinical…
What Is Gangliosidosis? Gangliosidosis encompasses a group of autosomal recessive lysosomal storage diseases caused by defects in lysosomal hydrolases or accessory proteins, leading to pathological accumulation of gangliosides within the central nervous system (CNS). Based on the defective protein, the…
Guangzhou MingCeler Biotech Signs Strategic MOU with Hankook Kinetico Engineering in South Korea to Roll Out Custom Gene-Edited Mouse Models 16/Jun/2026 Guangzhou MingCeler Biotech Co., Ltd. (“MingCeler Biotech”) has officially signed a strategic Memorandum of Understanding (MOU) with Daegu-based Hankook…
What Is Severe Congenital Neutropenia? Severe Congenital Neutropenia (SCN) is a rare inherited bone marrow failure syndrome characterized by arrested myeloid differentiation, with an estimated prevalence of 3–8.5 cases per million people. Due to profound neutropenia, patients suffer recurrent infections…
