CD63黑色素瘤標(biāo)記（鼠單克隆抗體）

廣州健侖生物科技有限公司

CD63是一種溶酶體膜蛋白，具有激活血小板表面抗原的活性。存在于多種不同類型細(xì)胞的胞膜和胞質(zhì)中，如淋巴組織、骨髓組織、內(nèi)皮細(xì)胞和黑色素瘤?？捎糜诤谏亓龅难芯?。

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【產(chǎn)品介紹】

細(xì)胞定位：細(xì)胞漿/細(xì)胞膜

克隆號(hào)：NK1/C3

同型：IgG1/K

適用組織：石蠟/冰凍

陽(yáng)性對(duì)照：黑色素瘤

抗原修復(fù)：熱修復(fù)（EDTA）

抗體孵育時(shí)間：30-60min

CD63黑色素瘤標(biāo)記（鼠單克隆抗體）

3.5 細(xì)胞的接種和培養(yǎng) 參照文獻(xiàn)進(jìn)行。
3.6 精原細(xì)胞的純化及其純度評(píng)估：分離細(xì)胞接種后，定時(shí)觀察貼壁情況。當(dāng)見(jiàn)到混雜其中的睪丸體細(xì)胞開始貼壁時(shí)，小心傾斜培養(yǎng)皿，將尚未貼壁的精原細(xì)胞連同培養(yǎng)液一起吸出，另行接種培養(yǎng)。待細(xì)胞貼壁后(大約培養(yǎng)12～24h)，棄去舊液，用PBS洗1～2次，加入新鮮培養(yǎng)液。任選3個(gè)視野，用計(jì)數(shù)器計(jì)每個(gè)視野中的細(xì)胞總數(shù)和精原細(xì)胞數(shù)(圓形的精原細(xì)胞附著在多突起的支持細(xì)胞上，呈鏈狀、葡萄串狀或以散在方式存在)，然后分別計(jì)算均值±標(biāo)準(zhǔn)差(0.gif (881 bytes)±s)。
4.電鏡樣品的制備
將新分離后位于27%～35% Percoll梯度間的細(xì)胞離心成團(tuán)，棄去培養(yǎng)液，加入2ml 2.5%戊二醛，4℃下預(yù)固定24h；PBS清洗后轉(zhuǎn)至1%的鋨酸中后固定2h，逐級(jí)丙酮脫水，Epon812包埋，超薄切片機(jī)切片，JEM-1 200EX Ⅱ電鏡觀察(分布在19%～27%及35%～43%Percoll梯度間的細(xì)胞太少，沒(méi)有制成電鏡樣品)。
結(jié)果
1.生精上皮的消化
4次消化所獲懸液量均為1.5ml。如表3所示，平均每10個(gè)睪丸可獲得4.219×106個(gè)細(xì)胞；其中活細(xì)胞、死細(xì)胞、細(xì)胞團(tuán)平均所占百分比依次為90.08%、9.92%和8.91%；平均每個(gè)睪丸可獲得4.136×105個(gè)細(xì)胞。
2.生精上皮細(xì)胞在Percoll梯度中的分布

我司還提供其它進(jìn)口或國(guó)產(chǎn)試劑盒：登革熱、瘧疾、流感、A鏈球菌、合胞病毒、腮病毒、乙腦、寨卡、黃熱病、基孔肯雅熱、克錐蟲病、違禁品濫用、肺炎球菌、軍團(tuán)菌、化妝品檢測(cè)、食品安全檢測(cè)等試劑盒以及日本生研細(xì)菌分型診斷血清、德國(guó)SiFin診斷血清、丹麥SSI診斷血清等產(chǎn)品。

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【公司名稱】 廣州健侖生物科技有限公司
【市場(chǎng)部】     歐

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【騰訊  】 
【公司地址】 廣州清華科技園創(chuàng)新基地番禺石樓鎮(zhèn)創(chuàng)啟路63號(hào)二期2幢101-103室

3.5 cell inoculation and culture reference literature.
3.6 Purification of spermatogonia and purity assessment: After seeding the cells, observe the adherence regularly. When you see the mixed testis cells began to adhere to the wall, carefully tilt the culture dish, the sperm cells have not yet attached together with the culture medium sucked out, inoculation and culture. After cells adherent (about 12 ~ 24h training), discard the old liquid, wash with PBS 1 ~ 2 times, add fresh medium. Choose 3 fields of view, count the total number of cells in each field of view and the number of spermatogonia (round spermatogonia attached to multiple protruding supporting cells in a chain, grape cluster or scattered manner) , Then calculate mean ± standard deviation (0.gif (881 bytes) ± s).
4. Electron microscopy sample preparation
Centrifugation of the newly isolated cells in a gradient of 27% -35% Percoll, discarding the medium, adding 2 ml of 2.5% glutaraldehyde and pre-fixing at 4 ° C for 24 h; washing with PBS to 1% osmium tetroxide Fixed for 2h, dehydrated by acetone, embedded in Epon812, sliced ??by ultrathin microtome, observed by JEM-1 200EX Ⅱ electron microscope (there are too few cells in the range of 19% -27% and 35% -43% Percoll gradient, Electron microscopy sample).
result
1. Digestion of germinal epithelium
4 times the amount of suspension obtained digestion were 1.5ml. As shown in Table 3, an average of 4.219 × 10 6 cells were obtained per 10 testes. The average percentages of living cells, dead cells and cell clusters were 90.08%, 9.92% and 8.91% respectively, and the average number of testicular cells was 4.136 × 105 cells.
2. The distribution of germinal epithelial cells in Percoll gradient