詳細介紹
CD2(T細胞、NK細胞)鼠單克隆抗體
廣州健侖生物科技有限公司
CD2具有調(diào)解活化的T細胞和胸腺細胞與抗原呈遞細胞和靶細胞粘附的功能。主要用于大多數(shù)外圍淋巴組織中的T淋巴細胞、NK細胞、胸腺皮質(zhì)細胞及T細胞來源的大多數(shù)惡性細胞的研究。
我司還提供其它進口或國產(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、軍團菌、化妝品檢測、食品安全檢測等試劑盒以及日本生研細菌分型診斷血清、德國SiFin診斷血清、丹麥SSI診斷血清等產(chǎn)品。
歡迎咨詢
歡迎咨詢
【產(chǎn)品介紹】
細胞定位:細胞膜
克隆號:AB75
同型:IgG
適用組織:石蠟/冰凍
陽性對照:扁桃體
抗原修復(fù):熱修復(fù)(EDTA)
抗體孵育時間:30-60min
產(chǎn)品編號 | 抗體名稱 | 克隆型別 |
OB042 | CD1a(細胞表面糖蛋白) | EP3622 |
OB043 | CD20(B細胞) | L26 |
OB044 | CD21(B細胞) | EP3093 |
OB045 | CD23(B細胞) | MRQ-57 |
OB046 | CD2(T細胞、NK細胞) | AB75 |
OB047 | CD3(T細胞) | MRQ-39 |
OB048 | CD30(Ki-1抗原) | Ber-H2 |
OB049 | CD31(內(nèi)皮細胞標記) | JC70 |
OB050 | CD34(內(nèi)皮細胞標記) | QBEnd/10 |
OB051 | CD35(濾泡樹突狀細胞) | EP197 |
OB052 | CD38(急性淋巴細胞白血病抗原) | SP149 |
OB053 | CD4(T細胞) | SP35 |
OB054 | CD43(T細胞) | MT1 |
OB055 | CD43(T細胞) | DF-T1 |
CD2(T細胞、NK細胞)鼠單克隆抗體
七、實驗用品
顯微鏡、目鏡測微尺、鏡臺測微尺、蓋玻片(22mm×22mm)、載玻片、滴管、雙層瓶、擦鏡紙、血球計數(shù)板、吸水紙、計數(shù)器。
八、實驗方法
(一)微生物細胞大小的測定
1、目鏡測微尺的校正
把目鏡的上透鏡旋下,將目鏡測微尺的刻度朝下輕輕地裝入目鏡的隔板上,把鏡臺測微尺置于載物臺上,刻度朝上。先用低倍鏡觀察,對準焦距,視野中看清鏡臺測微尺的刻度后,轉(zhuǎn)動目鏡,使目鏡測微盡與鏡臺測微尺的刻度平行,移動推動器,使兩尺重迭,再使兩尺的“0”刻度*重合,定位后,仔細尋找兩尺第二個*重合的刻度,計數(shù)兩重合刻度之間目鏡測微尺的格數(shù)和鏡臺測微尺的格數(shù)。因為鏡臺測微尺的刻度每格長10μm,所以由下列公式可以算出目鏡測微尺每格所代表的實際長度。
目鏡測微尺每格長度
例如:目鏡測微尺5小格正好與鏡臺測微尺5小格重迭,已知鏡臺測微尺每小格為10μm
目鏡測微尺上每小格長度為。
用同樣方法分別校正在高倍鏡下和油鏡下目鏡測微尺每小格所代表的長度。
由于不同顯微鏡及附件的放大倍數(shù)不同,因此校正目鏡測微尺必須針對特定的顯微鏡和附件(特定的物鏡、目鏡、鏡筒長度)進行,而且只能在該顯微鏡上重復(fù)使用,當更換不同顯微鏡目鏡或物鏡時,必須重新校正目鏡測微尺每一格所代表的長度??潭戎睾?/span>
我司還提供其它進口或國產(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、軍團菌、化妝品檢測、食品安全檢測等試劑盒以及日本生研細菌分型診斷血清、德國SiFin診斷血清、丹麥SSI診斷血清等產(chǎn)品。
想了解更多的產(chǎn)品及服務(wù)請掃描下方二維碼:
【公司名稱】 廣州健侖生物科技有限公司
【市場部】 楊永漢
【】
【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號二期2幢101-103室
Seven, experimental supplies
Microscope, eyepiece micrometer, mirror micrometer, cover glass (22mm × 22mm), slide, dropper, double bottle, lens cleaning paper, blood count board, absorbent paper, counter.
Eight, experimental methods
(A) Determination of microbial cell size
1, eyepiece measuring micrometer correction
Unscrew the upper lens of the eyepiece, the eyepiece micrometer scale down gently into the eyepiece spacer, the mirror micrometer scale placed on the stage, the scale up. First use the low power lens to observe and aim at the focal distance. When you see the scale of the microscope micrometer in the field of vision, turn the eyepiece so that the eyepiece micrometer will be parallel to the scale of the microscope micrometer. Move the pusher so that the two- Then make two feet of the "0" scale compley coincident, positioning, carefully looking for the second full coincidence of two feet of the scale, counting the coincidence between the coincidence of the eyepiece micrometer scale and the stage micrometer scale grid. Because the graduation of the microscope micrometer scale is 10 μm long, the actual length represented by each cell of the eyepiece micrometer can be calculated from the following formula.
Eyepiece micrometer scale length of each grid
For example: eyepiece micrometer 5 grid just coincides with the table micrometer 5 grid overlap, it is known that the stage micrometer scale each grid is 10μm
Eyepiece micrometer on the length of each cell.
Use the same method to correct the magnification and magnification of the eyepiece micrometer ruler, respectively, represented by each cell length.
Due to the different magnifications of different microscopes and accessories, the correction eyepiece micrometer should be made for specific microscopes and accessories (specific objectives, eyepieces, barrel lengths) and should only be reused on this microscope. When changing different microscopes Eyepiece or objective must be re-calibrated eyepiece micrometer every cell length represented. Scale coincidence