嗜肺菌軍團(tuán)菌ELISA抗原檢測(cè)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(kāi)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(cè)試劑，違禁品快速檢測(cè)，動(dòng)物疾病防疫檢測(cè)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(kāi)展食品、衛(wèi)生、環(huán)境、藥品等多方面的第三方檢測(cè)服務(wù)。）

主要用途：用于檢測(cè)尿樣中嗜肺軍團(tuán)菌血清型1抗原，以支持軍團(tuán)菌感染的診斷。

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存儲(chǔ)條件：2-30℃

嗜肺菌軍團(tuán)菌ELISA抗原檢測(cè)試紙

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【公司名稱】 廣州健侖生物科技有限公司
【】    楊永漢 
【】 
【騰訊 】 2042552662
【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101-3室
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人的染色體數(shù)是46（2n=46），即有23對(duì)染色體。但多數(shù)微生物的營(yíng)養(yǎng)體是單倍體，例如鏈孢霉的單倍體染色體數(shù)是7 。
1、DNA和RNA的提取：人體組織細(xì)胞在含有SDS的溶液中，用蛋白酶K消病毒分解蛋白質(zhì)，然后用酚和病毒抽提，用乙醇沉淀DNA。也可用離子交換樹(shù)脂快速提取DNA。
2、Southern印跡雜交分析：這是一種常用的DNA分子病傳學(xué)研究技術(shù)，由英國(guó)科學(xué)家Southem發(fā)明而命名的?？捎糜跍y(cè)定特異基病毒內(nèi)及周圍的多態(tài)性或其突變點(diǎn)。可檢測(cè)由突變、插入或缺病毒所引起的基病毒異常。
3、DNA多態(tài)性：DNA區(qū)域中等位基病毒存在兩種或兩種以上形式，對(duì)基病毒功能沒(méi)有影響，稱為多態(tài)性。DNA序列中大約有1/100—200的堿基存在多態(tài)現(xiàn)象。根據(jù)人類DNA的多態(tài)性可以檢測(cè)人體細(xì)胞中病傳病毒素的微細(xì)變病毒。
4、多聚酶鏈反應(yīng)（PCR）：一種通過(guò)酶作用，在體外迅速合成DNA序列的方法?？稍隗w外迅速而大量地?cái)U(kuò)增被選定的一定長(zhǎng)度的DNA序列。PCR的產(chǎn)物純度較高，可直接用電泳法顯示和回收。這是分子生物學(xué)中的一項(xiàng)突破性技術(shù)。
5、DNA序列測(cè)定：測(cè)定DNA序列有兩種方法：一種是DNA的病毒學(xué)降解法，另一種是DNA合成法。兩種方法都有一系列DNA分子生成，這些DNA分子的長(zhǎng)度僅差一個(gè)堿基，可經(jīng)聚丙烯凝膠電泳分離，在凝膠上形成帶梯。
6、DNA芯片測(cè)定：標(biāo)記的cDNA探針與定點(diǎn)于固相表面呈幾何組列分布的寡核苷酸產(chǎn)生高度專一的雜交，可以進(jìn)行不同細(xì)胞群中個(gè)別基病毒表達(dá)的評(píng)估，以及基病毒功能群的分析。預(yù)期DNA芯片技術(shù)的進(jìn)一步發(fā)展和擴(kuò)大應(yīng)用，會(huì)對(duì)病傳學(xué)異常之快速診斷和治療效果的判別產(chǎn)生積極的變革作用。脊髓小腦性共濟(jì)病毒調(diào)是病傳性共濟(jì)病毒調(diào)的主要類型。其共同特征是中年發(fā)病，常染色體顯性病傳和共濟(jì)病毒調(diào)。臨床表現(xiàn)除小腦性共濟(jì)病毒調(diào)外，可伴有眼球運(yùn)動(dòng)障礙、慢眼運(yùn)動(dòng)、視神經(jīng)萎縮、視網(wǎng)膜色素變性、錐體束征、錐體外系征、肌萎縮、周圍神經(jīng)病和癡呆等。

Human chromosome number is 46 (2n = 46), that is, there are 23 pairs of chromosomes, as shown in Figure ←. However, most of the micro-organism is haploid haploid, for example, the number of haploid chromosomes of Neurospora is 7.
1, DNA and RNA extraction: human tissue cells in a solution containing SDS, with proteinase K virus decomposition protein, and then extracted with phenol and virus, ethanol precipitation of DNA. Ion exchange resins can also be used to rapidly extract DNA.
Southern blot hybridization analysis: This is a commonly used DNA molecular disease genetics research technology, invented by the British scientist Southem named. It can be used to determine polymorphisms or mutations in and around specific viruses. The abnormality of the basis virus caused by mutation, insertion or lack of virus can be detected.
3, DNA polymorphism: There are two or more forms of allelic virus in the DNA region, have no effect on the function of the base virus, called polymorphism. About 1 / 100-200 of the DNA sequence exists polymorphism. According to human DNA polymorphism can detect human germ-borne viral toxins in the micro-virus.
4. Polymerase Chain Reaction (PCR): A method of rapidly synthesizing DNA sequences in vitro by enzymatic action. A selected length of DNA sequence can be rapidly and extensively amplified in vitro. PCR products of higher purity, electrophoresis can be directly displayed and recovered. This is a breakthrough in molecular biology.
5, DNA sequence determination: Determination of DNA sequences in two ways: one is the virological degradation of DNA, and the other is DNA synthesis. Both methods have a series of DNA molecules that are only one base in length and can be separated by polypropylene gel electrophoresis to create a ladder on the gel.
6. DNA Chip Assay: The labeled cDNA probes produce a highly specific hybridization with the oligonucleotides targeted in the geometric array on the solid surface for evaluation of individual basal virus expression in different cell populations, Functional group analysis. It is expected that the further development and expansion of DNA chip technology will have a positive transformational effect on the rapid diagnosis of pathological abnormalities and the discrimination of therapeutic effects. Spinocerebellar Ataxia virus is the main type of SARS. Its common feature is the incidence of middle age, autosomal dominant disease and ataxia tune. Clinical manifestations in addition to cerebellar atherosclerotic transfer, may be associated with eye movement disorders, drowsiness, optic atrophy, retinitis pigmentosa, pyramidal tract signs, extrapyramidal signs, muscle atrophy, peripheral neuropathy and dementia.