WebThe present invention relates to a protein derived from a microorganism belonging to the genus Bacillus, which has an activity of hydroxylating a compound represented by the formula (I-a): wherein R1 represents a hydrogen atom, a substituted or unsubstituted alkyl, or an alkali metal, and R2 represents a substituted or unsubstituted alkyl or a substituted or … WebTOYOBO CO., LTD. TOYOBO (SHANGHAI) BIOTECH, CO., LTD. Tel(81)-6-6348-3888 Tel (+86)-21-58794900 www.toyobo.co.jp/e/bio [email protected] . FOR RESEARCH USE …
PRODUCTS NGS/Single Cell GenNext™ NGS Library Prep Kit …
WebMar 3, 2024 · This protocol describes sgRNA design, preparation of lentiCRISPR-sgRNA vectors, functional validation of sgRNAs, preparation of lentiviruses, and lentiviruses transduction in adipocytes. Moreover, an optimized method of gene editing using the lentiCRISPRv2 vector expressing two sgRNAs targeting two different genes has also been … Web安韶雅,虎 娟,张 虹,孙 放,马 霞,王 晨,陈 任 (1.宁夏大学宁夏优势特色作物现代分子育种重点实验室,中国宁夏银川750021;2.宁夏大学西部特色生物资源保护与利用教育部重点实验室,中国宁夏银川750021;3.宁夏大学生命科学学院,中国宁夏银川750021) psychic love expert
Ligation high Ver.2 - 製品情報 バイオ事業総括部
WebThe ligation reaction is an essential step in genetic recombination experiments. For this reaction, T4 DNA ligase has been widely used. Ligation high Ver.2 is a highly efficient … TECHNOLOGY; MANUAL; SDS; PRINT. DESCRIPTION. KOD One TM PCR master … Source. E. coli strain that carries the cloned T7 RNA polymerase gene from T7 phage. … Ligation high Ver.2; TArget Clone™/ TArget Clone™ -Plus-10xA-attachment mix; KOD … Ligation high Ver.2; TArget Clone™/ TArget Clone™ -Plus-10xA-attachment mix; KOD … Toyobo has various modifying enzymes. The detailed information can be referred … Purified DNA fragments can be applied to sequencing, restriction enzyme … Ligation high Ver.2; TArget Clone/TArget Clone -Plus-10xA-attachment mix; … WebThe steps from terminal repair and 3' end adenylation to adapter ligation can be conducted in the same container. Terminal repair and adenylation at the 3' end can be WebApr 18, 2011 · pCV21::Tn5 (#1) and (#2) DNA were partially digested with XbaI, and the single-cut product was separated from non- or double-digested product by agarose gel electrophoresis, extracted and purified using MonoFas DNA Purification Kit I (GL Science); the gap of the 5′-end was filled with KOD polymerase (TOYOBO), ligation was carried out … psychic louise