福建农业学报
福建農業學報
복건농업학보
FUJIAN JOURNAL OF AGRICULTURAL SCIENCES
2013年
9期
884-887
,共4页
水稻%总蛋白提取%Western Blot
水稻%總蛋白提取%Western Blot
수도%총단백제취%Western Blot
rice%total protein extract%western blot
介绍一种简单快捷的水稻不同组织总蛋白提取方法。该方法采用预冷甲醇和丙酮依次洗涤去除杂质和次生代谢干扰物,同时在甲醇洗涤步骤中加入蛋白酶抑制剂混合液,能够最大限度地包含所有蛋白质并降低蛋白酶的降解作用,提高蛋白质的质量和产量。采用该方法从水稻的根、茎、叶及发育中的种子中提取粗蛋白,产量为20~99 mg ? g -1 FW ,提取蛋白整个过程耗时1.6 h 。以 SDS-PAGE 胶及 Western Blot 检测所提总蛋白的质量,分别用核蛋白、胞浆蛋白、膜蛋白以及淀粉结合型蛋白等不同类型蛋白抗体进行 Western Blot 检验。结果显示采用该方法所分离的总蛋白质量可以满足水稻不同类型蛋白对 Western Blot 的质量要求。
介紹一種簡單快捷的水稻不同組織總蛋白提取方法。該方法採用預冷甲醇和丙酮依次洗滌去除雜質和次生代謝榦擾物,同時在甲醇洗滌步驟中加入蛋白酶抑製劑混閤液,能夠最大限度地包含所有蛋白質併降低蛋白酶的降解作用,提高蛋白質的質量和產量。採用該方法從水稻的根、莖、葉及髮育中的種子中提取粗蛋白,產量為20~99 mg ? g -1 FW ,提取蛋白整箇過程耗時1.6 h 。以 SDS-PAGE 膠及 Western Blot 檢測所提總蛋白的質量,分彆用覈蛋白、胞漿蛋白、膜蛋白以及澱粉結閤型蛋白等不同類型蛋白抗體進行 Western Blot 檢驗。結果顯示採用該方法所分離的總蛋白質量可以滿足水稻不同類型蛋白對 Western Blot 的質量要求。
개소일충간단쾌첩적수도불동조직총단백제취방법。해방법채용예랭갑순화병동의차세조거제잡질화차생대사간우물,동시재갑순세조보취중가입단백매억제제혼합액,능구최대한도지포함소유단백질병강저단백매적강해작용,제고단백질적질량화산량。채용해방법종수도적근、경、협급발육중적충자중제취조단백,산량위20~99 mg ? g -1 FW ,제취단백정개과정모시1.6 h 。이 SDS-PAGE 효급 Western Blot 검측소제총단백적질량,분별용핵단백、포장단백、막단백이급정분결합형단백등불동류형단백항체진행 Western Blot 검험。결과현시채용해방법소분리적총단백질량가이만족수도불동류형단백대 Western Blot 적질량요구。
A simple and rapid applicable protocol for extracting high-quality proteins from rice tissues is described . In the protocol , precooling methanol and acetone is used to precipitate proteins and remove contaminants and secondary metabolites . Adding protease inhibitors in methanol for washing is include all proteins to maximize and reduce degradation of proteases .By using this protocol the total protein yield of different tissues were range from 20 to 99 mg ? g - 1 FW and the entire process taken 1.6 h . To evaluate the quality of the extracted protein ,SDS/PAGE gel and Western Blot were employed . 4 antibodys represented different protein type include the nucleoprotein antibody ,plasmosin antibody , membrane protein antibody and granule-bound starch protein antibody as first antibody for Western Blot . The results show the extraction of high-quality protein samples suitable for Western analysis ,and the overall quality of the protein profiles was good . The simplified protocol described here presents considerable savings of time and reagents .