吗啡（OPI）/巴比妥（BAR）检测试纸

吗啡（OPI)/巴比妥（BAR)检测试纸

广州健仑生物科技有限公司

广州健仑生物长期供应各种违禁品检测试纸、违禁品检测卡、违禁品检测试剂盒、药筛试纸、药筛试剂盒、吗啡检测试剂盒、巴比妥检测试剂盒等。

我司同时有bzo - bar - coc - thc met - - opi - oxy - mdma - cfp - amp - xtc – bat多联检测卡（胶体金法）

主营品牌：美国NovaBios、美国Cortez、国产创仑等等。

主要用途：筛查违禁品滥用残留、麻醉药残留、兴奋药物残留等等。

检测范围：吗啡、KET、mamp、MDMA、BZO、THC、巴比妥、MTD、BAR、MDMA、AMP、BUP、PCP、TCA、OXY、MET等等。

产品特点：可以根据需求自主订制多联卡。多联卡自由组合，从二联到十五联都可以订制。

我司还提供其它进口或国产试剂盒：登革热、疟疾、流感、A链球菌、合胞病毒、腮病毒、乙脑、寨卡、黄热病、基孔肯雅热、克锥虫病、违禁品滥用、肺炎球菌、军团菌、化妆品检测、食品安全检测等试剂盒以及日本生研细菌分型诊断血清、德国SiFin诊断血清、丹麦SSI诊断血清等产品。

如需订购或者了解请以下或

mob： 杨   ： 

【储存条件及有效期】

储存条件：原包装应储存于4～30℃避光干燥处，切忌冷冻。

有效期：24个月。

以下可以自由COMBO多联检测卡：

吗啡、巴比妥二联检检测试纸

吗啡、巴比妥二联检检测试纸

检测吗啡试纸/检测巴比妥测试纸

检测吗啡试纸/检测巴比妥测试纸

吗啡（OPI)/巴比妥（BAR)检测试纸

吗啡（OPI)/巴比妥（BAR)检测试纸

美国NOVABIOS多联检测杯简介：

美国NOVABIOS单卡产品简介：

【检验方法】w the test device, urine specimen, and/or controls to reach room temperature (15-30oC) prior to te

在进行检测前必须先完整阅读使用说明书，使用前将本品和尿样恢复至室温（20℃～30℃）。

• 撕开铝箔袋，取出试剂盒，应在1小时内尽快使用。
• 将试剂盒置于干净平坦的台面上，用塑料吸管垂直滴加3滴无空气泡的尿样（约100µL）于加样孔（S）中。
• 等待紫红色条带的出现，3～5分钟时直接观察结果，10分钟后判定无效。

【检测结果示意图】

INTERPRETATION OF RESULTS

（请参考上图）

【检验结果的解释】

阳性（+）：仅在控制区（C）出现一条紫红色条带，在检测区（T）无紫红色条带出现。阳性结果表明尿液中的浓度在阈值（3000ng/mL）以上。

阴性（-）：出现两条紫红色条带。一条位于检测区（T），另一条位于控制区（C）。阴性结果表明尿液中的因浓度在阈值（3000ng/mL）以下。

无效：控制区（C）未出现紫红色条带。表明操作不当或试剂盒已失效。在此情况下，应再次仔细阅读说明书，并用新的试剂盒重新测试。如果问题仍然存在，应立即停止使用此批号产品，并与当地供应商。

注意：检测区（T）紫红色条带可呈现颜色深浅的现象。但是，在规定的观察时间内，不论该色带颜色深浅，即使只有非常弱的色带也应判定为阴性结果。

更多产品说明可通过下方的进行了解

添加扫一扫二维码：

【公司名称】 广州健仑生物科技有限公司

【 市场部 】       杨永汉
【】 
【腾讯  】
【公司地址】 广州市清华科技园健新基地番禺石楼镇健启路63号二期2幢101-103室

After cytochrome staining or Wright's staining, the cytoplasm was blue and the nucleus was purple. The nucleus is located in the center of the worm body. The nucleus and the tip are dyed light red granules called the deputy nucleus. The free body can rotate in a spiral. Parasitic intracellular parasites are spindle-shaped or oval-shaped, and can reproduce in two ways: diploid, bisplit, and fission proliferation. They usually contain several to more than ten parasites. Pseudocyst (Fig. 12-5) is called a pseudo-encapsulation (Fig. 12-5) surrounded by a host cell membrane. When it is proliferated to a certain number, the membrane ruptures and the tachyzoites are released. The blood flow continues to other cells. Reproduction. Under the electron microscope, the tachyzoite dermis consists of two layers. The outer layer envelops the entire body. It is hollowed at the side edges to form cell-like micropores. The inner layer is slightly thicker and has a class at the front, side, and rear ends. Conoids and polar rings. The cone is composed of one or more groups of arched wires that spiral upward and hollow. The rhoptry 8 to 10 rods are gland-like structures that are the extensions of the cones. The nucleus is located in the second half of the worm body. The nucleoli position is indeterminate. The Golgi apparatus is often located in the depression of the nucleus. It is a cystic-like structure with one to several mitochondria. The worm body also has developed rough endoplasmic reticulum and lysosomes. And ribosomes (Figure 12-6). When the worm body undergoes splitting of the inner diploid buds, the organelles in the worms disappear, the leading edge of the nucleus divides into two protrusions, gradually expands to form two daughter nucleuses, all organelles are recovered, and the worm body splits into two worms. The capsule is round or elliptical in shape and has a diameter of from 5 μm to 100 μm. It has a layer of resilient, tough cysts. The cyst trophozoite called bradyzoite can be continuously proliferated, containing several to several hundred worms. Under certain conditions, it can be broken. The bradyzoites can re-enter new cells to form new cysts. Survive within the organization. Intestinal villous epithelial cells develop and proliferate. The mature schizonts are oblong in shape and contain 4 to 29 merozoites. They are mostly 10 to 15 in fan-like arrangement. The merozoites resemble crescents. Back blunt, smaller than trophozoites. In view of the deficiencies in Toxoplasma gondii etiology and advances in serum technology, serodiagnosis has become a widely used diagnostic tool today. There are many types of methods, mainly: 1. The dye test (DT test) is a classic, specific serological method using live trophozoites with the participation of specific agents in the sample under the influence of activating factors, so that the destruction of the worm's pellicle is not caused by the colorant Methylene Blue. Microscopic examination showed that the worm body was not positive for blue dyeing, and most of the worm body was sexually blue. 2. Indirect hemagglutination test (IHA) This method is specific, sensitive, and simple. It is suitable for epidemiological investigations and screening antibody tests. It is widely used.