美國NOVABIOS 嗎啡檢測(cè)板（快檢法）
| 型 號(hào)： | 違禁品檢測(cè)試紙 |
| 報(bào) 價(jià)： |  |
美國NOVABIOS 嗎啡檢測(cè)板（快檢法）：我司同時(shí)有bzo - bar - coc - thc met - - opi - oxy - mdma - cfp - amp - xtc – bat多聯(lián)檢測(cè)卡（膠體金法）
- 產(chǎn)品描述
美國NOVABIOS 嗎啡檢測(cè)板（快檢法）
廣州健侖生物科技有限公司
廣州健侖生物長期供應(yīng)各種違禁品檢測(cè)試紙、違禁品檢測(cè)卡、違禁品檢測(cè)試劑盒、藥篩試紙、藥篩試劑盒、嗎啡檢測(cè)試劑盒、巴比妥檢測(cè)試劑盒等。
我司同時(shí)有bzo - bar - coc - thc met - - opi - oxy - mdma - cfp - amp - xtc – bat多聯(lián)檢測(cè)卡（膠體金法）
主營品牌：美國NovaBios、美國Cortez、國產(chǎn)創(chuàng)侖等等。
主要用途：篩查違禁品濫用殘留、麻醉藥殘留、興奮藥物殘留等等。
檢測(cè)范圍：嗎啡、KET、mamp、MDMA、BZO、THC、巴比妥、MTD、BAR、MDMA、AMP、BUP、PCP、TCA、OXY、MET等等。
產(chǎn)品特點(diǎn)：可以根據(jù)需求自主訂制多聯(lián)卡。多聯(lián)卡自由組合，從二聯(lián)到十五聯(lián)都可以訂制。
我司還提供其它進(jìn)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(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SiFin診斷血清、丹麥SSI診斷血清等產(chǎn)品。
如需訂購或者了解請(qǐng)以下或
mob： 楊 ：
【儲(chǔ)存條件及有效期】
儲(chǔ)存條件：原包裝應(yīng)儲(chǔ)存于4～30℃避光干燥處，切忌冷凍。
有效期：24個(gè)月。
以下可以自由COMBO多聯(lián)檢測(cè)卡：
BAR巴比妥藥篩檢測(cè)試紙
BAR巴比妥藥篩檢測(cè)試紙
嗎啡科研用快篩試劑盒
嗎啡科研用快篩試劑盒
健侖單卡檢測(cè)違禁品快檢法-嗎啡
健侖單卡檢測(cè)違禁品快檢法-嗎啡
進(jìn)口嗎啡尿液檢測(cè)杯
進(jìn)口嗎啡尿液檢測(cè)杯
美國NOVABIOS 嗎啡檢測(cè)板（快檢法）
美國NOVABIOS多聯(lián)檢測(cè)杯簡介：
產(chǎn)品名稱 | 規(guī)格 | 檢測(cè)違禁品類型 |
違禁品十聯(lián)檢測(cè)杯 | 25T/盒 | MET.AMP.MTD.THC.BAR.TCA.COC.BZO.PCP.OPI |
違禁品十三聯(lián)檢測(cè)杯 | 25T/盒 | AMP.BAR.BZO.COC.MET.MOR.MTD.PCP.PPX.TCA.THC.XTC.WADU |
違禁品十二聯(lián)檢測(cè)杯 | 25T/盒 | BZO.BAR.COC.THC.MET.OPI.OXY.MDMA.PCP.AMP.BUP.MTD |
美國NOVABIOS單卡產(chǎn)品簡介：
【檢驗(yàn)方法】w the test device, urine specimen, and/or controls to reach room temperature (15-30oC) prior to te
在進(jìn)行檢測(cè)前必須先完整閱讀使用說明書，使用前將本品和尿樣恢復(fù)至室溫（20℃～30℃）。
- 撕開鋁箔袋，取出試劑盒，應(yīng)在1小時(shí)內(nèi)盡快使用。
- 將試劑盒置于干凈平坦的臺(tái)面上，用塑料吸管垂直滴加3滴無空氣泡的尿樣（約100µL）于加樣孔（S）中。
- 等待紫紅色條帶的出現(xiàn)，3～5分鐘時(shí)直接觀察結(jié)果，10分鐘后判定無效。
【檢測(cè)結(jié)果示意圖】
INTERPRETATION OF RESULTS
（請(qǐng)參考上圖）
更多產(chǎn)品說明可通過下方的進(jìn)行了解
添加掃一掃二維碼：
【公司名稱】 廣州健侖生物科技有限公司
【 市場(chǎng)部 】 楊永漢
【】
【騰訊 】
【公司地址】 廣州市清華科技園健新基地番禺石樓鎮(zhèn)健啟路63號(hào)二期2幢101-103室
Anti-amoeoba antibodies can also bind to the surface of the parasites, agglutinating the trophozoites through lectins, and acting as an auxiliary agent for anti-infection or infection control. Some antibodies may migrate or be ingested due to the fluidity and endocytosis of cell membranes. In cells, the effect of antibodies is affected [15]. The functional antigens of Entamoeba histolytica are weak and do not stimulate the body to produce strong protective antibodies. Therefore, the protective immune function of the host is not strong. After the infection of Entamoeba histolytica, there is no long-lasting immunity. After repeated infections can still be repeated. The virus is also closely related to amoeba. Since Diamourid (1972) first discovered similar plant baculovirus particles in amoeba within the dissolved tissue, many virus particles have been found in amoeba, such as HIV. (HIV), Rotavirus, and Reovirus, etc. In 1976, Diamond LS also found that there are three main structural forms of viruses in amoeba within the dissolved tissue, namely, icosahedral, filamentous, and streak-like structures. . Entamoeba histolytica carries many virus particles, like the hepatitis virus plasmid. It can be seen that amoeba is one of the better vectors for viral particles. It is unclear whether the virus particles present in amoeba cells can be transfected into the body and cause host cell pathological changes. Bacteria's action Under the synergistic action of certain bacteria, Entamoeba histolytica can produce a stronger pathogenic effect on the organism. It can not only absorb foods decomposed by bacteria in the intestine, but also utilize the physicochemical conditions provided by the bacteria to multiply. Activities can even eat bacteria directly. Tests have shown that neither the pure cysts nor the pure bacteria ingest the disease, but the cysts that ingest mixed bacteria have the symptoms of acute amoebic dysentery. This is because bacteria can cause a suitable redox potential and hydrogen ion concentration, promote the proliferation of amoeba and the secretion of amoebic toxins, thereby weakening the host's systemic or local resistance. Bacteria can also directly damage the body's intestinal mucosa, providing favorable conditions for the body to invade the intestinal tissue. Some gram-positive bacteria and amoeba mixed culture can significantly increase the infection rate and the degree of disease in experimental animals; bacteria attached to the surface of trophozoites, but also with mannose-binding lectin or amoeba 260 ku half Lactose/acetylgalactosylagglutinin enhances the solubility of amoeba in host cells. Entamoeba histolytica isolates have great variability in their toxicity characteristics. Amoeba from different regions and different hosts has different toxicity.
