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- 详细信息
- 文献和实验
- 技术资料
- 规格:
100 µg
蛋白名称:BCL6蛋白, BCL6 protein
蛋白构建:A DNA sequence encoding the human BCL6 (P41182) N-terminal fragment (Met 1-Met 150) was fused with a Trx and a polyhistidine tag at the N-terminus.
表达宿主:E. coli
蛋白纯度:> 92 % as determined by SDS-PAGE
蛋白活性:0
蛋白内毒素:Please contact us for more information.
预测N端:Met
蛋白分子量:The recombinant human BCL6/Trx fusion protein consisting of 309 amino acids and has a calculated molecular mass of 34.2 kDa. It migrates as an approximately 33 kDa band in SDS-PAGE under reducing conditions.
蛋白NP号:P41182
蛋白氨基酸序列:Met1-Met150
蛋白标签:N-Trx & His
蛋白保存条件:Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
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文献和实验Double immunohistochemistry for BCL6 and PNA for Germinal Center detection.
. The secondary antibody should be absorbed against human and mouse serum; if not add 1 human and 1 mouse serum before use. Use Dako or Vector at 1:200 - 1:300 dilution. 7- Wash twice in TBS-T. 7bis- block endogenous peroxidase by incubating in 0.1NaN3
Double immunohistochemistry for BCL6 and PNA for Germinal Center detection
Double immunohistochemistry for BCL6 and PNA for Germinal Center detection. (on fixed, paraffin-embedded sections) Cut sections at 4µm, use a clean water bath with distilled water, and let the sections dry
质,小分子或是金属。当融合有亲和标签的蛋白通过标签-配体作用结合再层析基质上时,通过洗杂步骤,即可去除掉其他的细胞成分。 为了洗脱所需要的蛋白质,通过改变缓冲液的条件,如pH,或通过竞争亲和标签和配体连接的方法来进行。 但怎样的纯化是较为成功的呢?仅达到所需的质量量级,如毫克级(或克级)即可满足吗? 这些并不简单。质在蛋白纯化中同样尤为重要,比如,就蛋白的生物活性和纯度而言,通常会有所要求。 以下我们来讨论并且比较2种技术: His-tag系统和Strep-tag®系统,都使用了亲和层析法来纯化
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