檢測液體含違禁品快檢試紙

檢測液體含違禁品快檢試紙

廣州健侖生物科技有限公司

廣州健侖生物科技有限公司是集研制開發(fā)、銷售、服務(wù)于一體的優(yōu)良企業(yè),公司產(chǎn)品涉及臨床快速診斷試劑、食品安全檢測試劑，違禁品快速檢測，動(dòng)物疾病防疫檢測試劑，免疫診斷試劑、臨床血液學(xué)和體液學(xué)檢驗(yàn)試劑、微生物檢驗(yàn)試劑、分子生物學(xué)檢驗(yàn)試劑、臨床生化試劑、有機(jī)試劑等眾多領(lǐng)域，同時(shí)核心代理Panbio、FOCUS、Qiagen、IBL、CORTEZ、Fuller、Inbios、BinaxNOW、LumuQuick、日本富士、日本生研等多家有名診斷產(chǎn)品集團(tuán)公司產(chǎn)品，致力于為商檢單位、疾病預(yù)防控制中心、海關(guān)出入境檢疫局、衛(wèi)生防疫單位,緝毒系統(tǒng)，戒毒中心，檢驗(yàn)檢疫單位、生化企業(yè)、科研院所、醫(yī)療機(jī)構(gòu)等機(jī)構(gòu)與行業(yè)提供*、高品質(zhì)的產(chǎn)品服務(wù)。此外，本公司還開展食品、衛(wèi)生、環(huán)境、藥品等多方面的第三方檢測服務(wù)。

廣州健侖生物長期供應(yīng)各種違禁品檢測試紙、違禁品檢測卡、違禁品檢測試劑盒、藥篩試紙、藥篩試劑盒、嗎啡檢測試劑盒、巴比妥檢測試劑盒等。

使用說明書

【產(chǎn)品名稱】

通用名稱：檢測液體含違禁品快檢試紙

英文名稱：Diagnostic Kit for Nicotine（Colloidal Gold）

【包裝規(guī)格】 

1人份/袋、40人份/盒

Multi DOA Screen Panel are rapid chromatographic immunoassays for the qualitative and simultaneous detection of one to fourteen of the following drugs in a variety of combinations in human urine. The designed cutoff concentrations and direct calibrator for these drugs are as follows:

The test is used to obtain visual qualitative result and is intended for health care professionals use including professionals at point of care sites to assist in the determination of drug compliance. It is not intended for over the counter sale to non-professionals.

This assay provided only a preliminary analytical test result. A more specific alternative chemical method must be used in order to obtain a confirmed analytical result. Gas Chromatography/ Mass Spectrometry (GC/MS) or Liquid Chromatography/ Mass Spectrometry (LC/MS) are the preferred confirmatory method. Clinical consideration and professional judgment should be applied to any drug of abuse test result, particularly when preliminary positive results are indicated.

本品采用競爭抑制法和膠體金免疫層析技術(shù)，用于定性檢測人體尿液中尼古丁，適用于尼古丁藥物濫用的初步篩查。

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、食品安全檢測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以下或

mob： 楊   ： 

美國NOVABIOS多聯(lián)檢測杯簡介：

美國NOVABIOS單卡產(chǎn)品簡介：

w the test device, urine specimen, and/or controls to reach room temperature (15-30oC) prior to t

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

主流的模型認(rèn)為在細(xì)胞 進(jìn)化的zui初階段，原核細(xì)胞基因  組復(fù)制后并不伴有典型的無絲分 裂，而是擬核附近的細(xì)胞膜內(nèi)陷  形成雙層膜，將其中一個(gè)基因組 包圍、隔離，進(jìn)而發(fā)生細(xì)胞分裂  。未分裂出來的子細(xì)胞則緩慢演 化為細(xì)胞核、線粒體和葉綠體等  高度特化的細(xì)胞結(jié)構(gòu)。不足之處 ：實(shí)驗(yàn)證據(jù)不多無法解釋為何線  粒體、葉綠體與細(xì)菌在DNA分子 結(jié)構(gòu)和蛋白質(zhì)合成性能上有那么多  相似之處對線粒體和葉綠體的 DNA酶、RNA酶和核糖體的來源也很  難解釋。真核細(xì)胞的細(xì)胞核 能否起源于細(xì)菌的核區(qū)？線粒體基因  組中基因的數(shù)量很少，規(guī)模 遠(yuǎn)小于細(xì)菌基因組。但內(nèi)共生學(xué)說認(rèn)  為線粒體源于被吞噬的細(xì)菌 ，那么兩者基因組規(guī)模應(yīng)該較為相似  。為了解釋這一現(xiàn)象，有猜 想認(rèn)為原線粒體的基因除了丟失了一  些外，大部分轉(zhuǎn)移到了宿主 細(xì)胞的細(xì)胞核中，所以核基因編碼了  在超過%的線粒體表達(dá)內(nèi)的 蛋白質(zhì)。某些有線粒體，但線粒體中不  含DNA的生物（如隱孢子 蟲等）的mtDNA可能已*丟失或整合入  核DNA中。線粒體DNA（ mtDNA）在線粒體中有-個(gè)備份，呈雙鏈環(huán)  狀（但也有呈線狀的 特例存在）。
The mainstream model believes that in the initial stages of cell evolution, the prokaryotic genome replicated without the typical amitosis, but that the membrane surrounding the mimicry nucleus is invaginated to form a bilayer membrane, surrounding and isolating one of the genomes. Cell division. Undivided daughter cells slowly evolve into highly specialized cell structures such as nuclei, mitochondria, and chloroplasts. Inadequacies: There is not much experimental evidence to explain why mitochondria, chloroplasts, and bacteria have so many similarities in DNA molecular structure and protein synthesis performance. It is also difficult to explain the sources of mitochondria and chloroplast DNA enzymes, RNases, and ribosomes. . Can the eukaryotic cell nucleus originate from the bacterial nuclear region? The number of genes in the mitochondrial genome is small and much smaller than the bacterial genome. However, the symbiosis theory says that mitochondria are derived from phagocytosed bacteria, so the two genomes should be similar in size. In order to explain this phenomenon, it is thought that the original mitochondrial gene was transferred to the nucleus of the host cell except for a few. Therefore, the nuclear gene encodes more than 1% of the mitochondrial protein. Some mitochondria, but the mtDNA of mitochondria that do not contain DNA (such as Cryptosporidium, etc.) may have been compley lost or integrated into the nuclear DNA. Mitochondrial DNA (mtDNA) is duplicated in the mitochondria and is double-stranded (but there are linear special cases).