想被大鸡吧操,草草在线祝频,久久无视频码,日韩在线精品看看,日韩一区久久久色婷婷,精品粉嫩久久久懂色,97超碰青青色青青爱,黄色视频在线观看福利,影音先锋美味人妻

English | 中文版 | 手機(jī)版 企業(yè)登錄 | 個(gè)人登錄 | 郵件訂閱
生物器材網(wǎng) logo
生物儀器 試劑 耗材
當(dāng)前位置 > 首頁 > 技術(shù)文章 > Fluorescent Staining of Cells

Fluorescent Staining of Cells

瀏覽次數(shù):1779 發(fā)布日期:2012-6-20  來源:SciMall科學(xué)在線
1. Fluorescent phalloidin in methanol. Phallacidin does not work as well. Dilute 10 ul 330 nM stock into 500 ul PBS for each large coverslip.
2. PBS, solution A.
Procedure:
1. Fix and permeabilize cells (see other protocols). Mount coverslip onto a plastic frame reserved for fixed samples. Apply some vacuum grease to the frame before use, if necessary.
2. Turn off light. Dilute fluorescent phalloidin 50x into PBS.
3. Gently pipet phalloidin solution onto coverslip. Stain for 30 min at room temperature.
4. Rinse coverslip 3x with PBS.
5. Fill the chamber with PBS or an antibleaching solution and observe. Dishes may be stored at 4o in a sealed, light-tight container.
 
Immunofluorescence Staining
Materials:
1. PBS/BSA: PBS solution A with 1% BSA (Boehringer Mannheim 100 350) and 0.1% NaN3, stored at 4oC. Bring to room temperature before use.
2. Primary antibody, diluted appropriately with PBS/BSA. Need 200 ul per 45x50 coverslip. Clarify in a Eppendorf for 15 min (minimal requirement) or in an ultracentrifuge with the Type 42.2Ti rotor (or Airfuge) if necessary.
3. Secondary antibody, prepared as for the primary antibody.
4. Coverslip boxes.
Procedure (do not allow coverslips to dry out anytime):
1. Fix and permeabilize cells (see other protocols). Wash with PBS/BSA for 10 min in a fixation box.
2. Cut a small piece of parafilm to match the area of staining and put 200 ul antibody solution on the piece. Shake off most of the liquid from the coverslip but do not let it dry out. Invert the coverslip onto the parafilm. Prepare a 100 mm plastic petri dish containing a piece of wet filter paper. Place 2 wooden sticks in the dish and put coverslip upside down on the sticks. Seal the dish into a ziplock bag and place in the incubator. Stain 45 min at 34-37oC with the primary antibody, or overnight at 4oC.
3. Wash gently 3x, 10 min each, with PBS/BSA on a shaker. Fill a coverslip box with PBS/BSA and sink the coverslip to the bottom. The covering parafilm should float up.
4. Stain 30 min with the secondary antibody as in step 2.
5. Wash as in step 3.
6. Mount the coverslip onto a plastic frame reserved for fixed coverslips. Apply some vacuum grease to the frame before use, if necessary. Fill the chamber with PBS or an antibleaching solution and observe. Dishes may be stored at 4o in a sealed, light -tight container.
 
與本技術(shù)相關(guān)的試劑:
PE熒光標(biāo)記抗體
FITC熒光標(biāo)記抗體
其他熒光標(biāo)記抗體
發(fā)布者:上海睿之生物醫(yī)藥科技有限公司
聯(lián)系電話:021-64689011
E-mail:service@scimall.cn

標(biāo)簽: Fluorescent stain cell
用戶名: 密碼: 匿名 快速注冊 忘記密碼
評論只代表網(wǎng)友觀點(diǎn),不代表本站觀點(diǎn)。 請輸入驗(yàn)證碼: 8795
Copyright(C) 1998-2026 生物器材網(wǎng) 電話:021-64166852;13621656896 E-mail:info@bio-equip.com
阜平县| 榆社县| 抚宁县| 鸡东县| 太仆寺旗| 鞍山市| 定南县| 科技| 富宁县| 商城县| 元氏县| 汉源县| 彰武县| 若尔盖县| 万年县| 威宁| 弋阳县| 白河县| 方正县| 河池市| 本溪| 都昌县| 师宗县| 延寿县| 云安县| 文化| 扶余县| 上蔡县| 剑河县| 昌平区| 兰西县| 沂源县| 玉林市| 盐津县| 林西县| 江山市| 新安县| 遂溪县| 贵阳市| 静宁县| 贡嘎县|