英文名称:SDS-PAGE Stacking Gel Buffer 纯度:99 % 产地:中国/上海 品牌:泽叶生物 包装规格:500 mL 货号:ZY100867 别名:SDS-PAGE浓缩胶配胶液 SDS-PAGE浓缩胶配胶液(SDS-PAGE Stacking Gel Buffer)产品及特点 本产品专门用于配制非联续SDS-PAGE胶的浓缩胶,其浓度为4×,配胶时即开即用,非常方便。
Bio-Rad伯乐Stacking Gel Buffer预混制胶缓冲液(PH6.8)1610799 1L,0.5M Tris-HCl,pH 6.8。Bio-Rad 提供多种预混制胶缓冲液,可用于制备Native或SDS-PAGE凝胶的浓缩和分离胶。 Use Resolving Gel Buffer when casting your own polyacrylamide protein gels. This buffer is used to cast the resolving (sieving)...
英文别名: ACRYLAMIDE 2K - STACKING GEL SOLUTION (4 %) FOR SDS-PAGE中文名: 中文别名: CBNumber: CB71506142 分子式: C3H5NO 分子量: 71.0779 MOL File: Mol file 化学性质 安全信息 用途 供应商 1 ACRYLAMIDE 2K - STACKING GEL SOLUTION (4 %) FOR SDS-PAGE化学性质 ...
In this method, the urine protein samples are run into the stacking gel by SDS-PAGE where it is concentrated into a single band, and then quickly stained by 0.001% Coomassie at high temperature. High correlations were found between the BSA and urine protein standards (R2 = 0.997 and R2 =...
1L,0.5M Tris-HCl,pH 6.8。Bio-Rad 提供多种预混制胶缓冲液,可用于制备Native或SDS-PAGE凝胶的浓缩和分离胶。 Use Resolving Gel Buffer when casting your own polyacrylamide protein gels. This buffer is used to cast the resolving (sieving) portion of SDS or native gels. ...
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SDS-PAGE进行描述与PROTEAN II电泳装置(BIO-RAD)的Laemmli(1970),使用4%的浓缩胶和12%的丙烯酰胺凝胶。 翻译结果2复制译文编辑译文朗读译文返回顶部 SDS 页根据说明被 Laemmli 实行 (1970 年 ) 利用一个 Protean II 电脉单位 ( 生物拉德 ) 使用 4% 成堆凝胶体和 12% 运行 acrylamide 凝胶体。 翻译结果3复...
and stacking gel boundary of conventional one-step SDS-PAGE gels can be unclear.Dye was added to the stacking gel of the one-step gel.A colored stacking gel helps confirm successful gel preparation before SDS-PAGE.The new one-step gel performed comparably to conventional one- and two-step ...
Tris也称Tris base或2-Amino-2-(hydroxymethyl)-1,3-propanediol。分子式为C4H11NO3,分子量为121.14; 4×Tris-HCl-SDS浓缩胶缓冲液中含有0.5 M Tris base,0.4% SDS,用HCl调至pH6.8,25℃。用于SDS-PAGE上层浓缩胶的配制。配制时无需再加10% SDS。 本品为4倍浓缩液,使
SgP450,SgUGT269-1, andSgUGT289-3using the specific primers (Table S3) via KOD One PCR Master Mix.Atactin(Accession number: NM_001338359) was used as positive control. WT plants was the negative control. The gene expression of transgenes inArabidopsiswere analyzed with DNA gel ...