SCA® DNA Fragmentation is a module for the counting of DNA fragmented and non fragmented spermatozoa, in human samples treated with kits based on the Sperm Chromatin Dispersion (SCD). available for Veterinary and Toxicology.

SCA® CASA System for semen analysis allows the accurate, repetitive and automatic assessment of the following sperm parameters: motility, concentration, morphology, DNA fragmentation, vitality, acrosome reaction and leukocytes. More information: Semen test following WHO laboratory manual.

The SCA (Sperm Class Analyzer) CASA System is a modular automatic software for the analysis of concentration, motility, morphology, DNA fragmentation, vitality and acrosome reaction of human and animal sperm samples, and besides, leukocytes for human.

SCA® DNA Fragmentation is a module for the counting of DNA fragmented and non fragmented spermatozoa, in human samples treated with kits based on the Sperm Chromatin Dispersion (SCD) as GoldCyto DNA. Spermatozoa are recognized and classified automatically into fragmented or non fragmented spermatozoa, following the established analysis criteria

MULTI-PATIENT: With the SCA SCOPE you can analyze several patients at the same time. EASY TO USE: The device can be used by anyone with no prior knowledge of microscopy. Reports can be printed directly. BIG DATA: All results are stored in a database with support for complex statistics, custom queries and integration with a LIS.

2022年2月23日 · Evidence that long non-coding RNAs (lncRNAs) participate in DNA repair is accumulating, however, whether they can control DNA repair pathway choice is unknown. Here we show that the small Cajal...

SCA® DNA Fragmentation VET. Module for the automatic counting of DNA fragmented and non fragmented spermatozoa, in animal samples treated with kits based on the Sperm Chromatin Dispersion (SCD) as Halomax® DNA fragmentation identifies a unique mark of apoptosis, and is usually associated with structural changes in cellular morphology

2023年12月22日 · SCA-seq利用纳米孔技术对包含染色质可及性、CpG甲基化和染色质构象信息的长片段进行测序，在单分子分辨率上将染色质可及性和CpG甲基化映射到基因组空间结构，同时解析基因组构象。 基因组在细胞内具有三维结构，这使得基因组区域的可及性具有类似的空间复杂性，其表观基因组信息也具有复杂的空间排列。 因此，有必要使用精密的工具来深入研究染色质可及性，从而全面理解染色质活化和基因的相互作用。 值得注意的是，仅依靠解析染色质的可及 …

脊髓小腦性共濟失調 (SCA)是一種以小腦功能失調為主要病徵的遺傳性神經系統退化疾病。 以致病基因作為分類，已知的SCA特定類型已達31種之多。 SCA的遺傳基制是常染色體顯性遺傳，這是指在一對基因中只要其中一個存在致病的突變便足以引起病徵。 致病的基因突變可以由男或女性患者傳到下一代。 每一個第二代都有50%機會遺傳到致病的基因突變，男女的遺傳機會相同。 如何診斷一個特定類型的SCA？ 要診斷SCA，首先需要的是對病徵及病情的發展作出臨床評估。 …

Spinocerebellar ataxia (SCA) is one of a group of genetic disorders characterized by slowly progressive incoordination of gait and is often associated with poor coordination of hands, speech, and eye movements.