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PCR核酸試劑 糞便寄生蟲多重檢測PCR熒光試劑盒
廣州健侖生物科技有限公司
單管多重檢測溶組織內(nèi)阿米巴,隱孢子蟲屬,賈第鞭毛蟲和內(nèi)部對照。
One tube multiplex for detection of Entamoeba histolytica, Cryptosporidium spp., Giardia lamblia and internal control.
PCR核酸試劑 糞便寄生蟲多重檢測PCR熒光試劑盒
JL-FT017 | 呼吸道病原體16種多重檢試劑盒(PCR方法) | Respiratory pathogens 16 |
JL-FT018 | 人腺病毒/偏肺病毒/博卡病毒聯(lián)合檢測試劑盒(PCR方法) | HAdV/HMPV/HBoV |
JL-FT019 | 甲型流感病毒亞型H1N1,H3NX,H5NX和H7NX檢測試劑盒(PCR方法) | Flu differentiation |
JL-FT020 | 肺炎鏈球菌/金色葡萄球菌/卡他莫拉菌/流感嗜血桿菌四聯(lián)檢測試劑盒(PCR方法) | SPn/Staph/MC/HI |
JL-FT021 | 人副流感病毒四重檢測試劑盒(PCR-熒光探針法) | HPIV |
JL-FT022 | 腸道病毒/帕氏病毒/腺病毒三重聯(lián)合檢測試劑盒(PCR方法) | EPA |
JL-FT023 | 腸道病毒/帕氏病毒/腺病毒多重檢測PCR熒光試劑盒 | EPA |
JL-FT024 | 病毒性胃腸炎的6種病原體聯(lián)合檢測試劑盒(PCR-熒光探針法) | Viral gastroenteritis |
JL-FT025 | 病毒性胃腸炎六聯(lián)檢測試劑盒(PCR-熒光探針法) | Viral gastroenteritis |
JL-FT026 | 細菌性腸胃炎的9種菌屬聯(lián)合檢測試劑盒(PCR-熒光探針法) | Bacterial gastroenteritis |
JL-FT027 | 細菌性腸胃炎菌屬9聯(lián)PCR熒光檢測試劑盒 | Bacterial gastroenteritis |
JL-FT028 | Stool parasites | |
JL-FT029 | 諾如病毒G1/G2檢測試劑盒(PCR-熒光探針法) | Noro |
JL-FT030 | 諾如病毒G1/G2分型雙重熒光PCR檢測試劑盒 | Noro |
JL-FT031 | 艱難梭菌多重檢測試劑盒(PCR-熒光探針法) | C.difficile |
JL-FT032 | 沙眼衣原體/淋球菌/生殖支原體多重熒光PCR檢測試劑盒 | Urethritis basic |
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。
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【公司名稱】 廣州健侖生物科技有限公司
【市場部】 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號二期2幢101-103室
(2)柱上吸附的過度標記蛋白可繼續(xù)增加NaCl的濃度至
2.0mol/L洗脫完。
經(jīng)過DEAE-纖維素層析后的標記抗體,其抗體量一般約損失50%,因此有些要求不太高的抗體,如抗細菌熒光抗體,不一定要這樣處理,可用染色效價測定的稀釋法除去非特異性染色。
(五)熒光抗體稀釋法
先測定熒光抗體特異性染色與非特異性染色的效價,若二者效價相差較大,則可將熒光抗體稀釋至一臨界濃度,使特異性染色呈陽性,而使非特異性染色保持陰性,稀釋方法和染色效價測定方法相同。
(六)純化抗原法
用各種方法提純單一成分的抗原是產(chǎn)生單價特異性抗體的zui主要條件。近代免疫化學技術(shù)(免疫吸收法)和柱層析法等提供了很大的可能性,可參考有關(guān)專著。
(七)純化抗體法---免疫吸收法
例如抗IgA血清的純化方法---免疫吸收法。如分泌型IgA( SIgA)抗原純度不高,所制的抗血清常與IgG呈交叉反應(yīng),為此需要吸收,常采用純化的人IgG戊二醛聚合物加以吸收純化。
(2) Over-labeled protein adsorbed on the column can continue to increase the concentration of NaCl to
2.0mol / L eluting finished.
After DEAE-cellulose chromatography of the labeled antibody, the amount of antibody is generally about 50% loss, so some less demanding antibodies, such as anti-bacterial fluorescent antibodies, do not have to deal with this method can be used to determine the dilution of the dye titer Non-specific staining is removed.
(E) Fluorescent antibody dilution method
First determine the fluorescent antibody-specific staining and non-specific staining titer, if the difference between the two titer, you can dilute the fluorescent antibody to a critical concentration, so that specific staining was positive, leaving non-specific staining remained negative, The same dilution method and determination of the titer.
(Vi) Purified antigen method
Purification of a single component of antigen by various means is the most important condition for the production of monovalent specific antibodies. Modern immunochemical techniques (immunosuppression) and column chromatography provides a great possibility, you can refer to the monograph.
(G) Purified antibody method --- immunosorbent assay
For example, anti-IgA serum purification method --- immune absorption method. Such as secreted IgA (SIgA) antigen purity is not high, the resulting antisera often cross-react with IgG, which needs to be absorbed, often using purified human IgG glutaraldehyde polymer to be purified by absorption.