- 產品描述
PCR試劑 細菌性腸胃炎的9種菌屬PCR核酸檢測試劑盒
廣州健侖生物科技有限公司
兩種準備使用lyo master混合物(各8孔條),用于檢測結腸彎曲桿菌/空腸彎曲菌/紅嘴鷗彎曲桿菌,艱難梭菌,大腸桿菌Verooxin陽性,沙門氏菌屬,志賀氏菌屬,腸侵襲性大腸桿菌,小腸結腸炎耶爾森氏菌包括內部對照。
Two ready to use lyo master mixes (8-well strips each) for detection of Campylobacter coli/jejuni /lari, Clostridium difficile, Escherichia coli verotoxin positives, Salmonella spp., Shigella spp., enteroinvasive Escherichia coli, Yersinia enterocolitica and internal control
PCR試劑 細菌性腸胃炎的9種菌屬PCR核酸檢測試劑盒
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種病原體聯合檢測試劑盒(PCR-熒光探針法) | Viral gastroenteritis |
JL-FT025 | 病毒性胃腸炎六聯檢測試劑盒(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PCR熒光檢測試劑盒 | Bacterial gastroenteritis |
JL-FT028 | 糞便寄生蟲多重檢測PCR熒光試劑盒 | 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診斷血清等產品。
歡迎咨詢
歡迎咨詢2042552662
PCR試劑
想了解更多的產品及服務請掃描下方二維碼:
【公司名稱】 廣州健侖生物科技有限公司
【市場部】 楊永漢
【】
【騰訊 】 2042552662
【公司地址】 廣州清華科技園創新基地番禺石樓鎮創啟路63號二期2幢101-103室
二、消除非特異性染色的方法
消除熒光抗體非特異性染色的方法應根據產生的原因采取適當的方法,常用的方法有以下幾種:
(一)動物臟器粉末吸收法
常用肝粉(豬、大白鼠或小白鼠),其次是骨髓粉、鼠腦粉和雞胚粉等。每毫升熒光抗體中加入肝粉50~100mg,在離心管中充分混勻,在室溫中振動2h,4℃中過夜,再攪拌10min,高速離心(3000~15000r/min)30min,1~2次后,即可使用其上清液。吸收一般應在臨用前進行,吸收后之熒光抗體保存冰箱中勿超過2周。染色應作吸收前后之比較,吸收時可先用緩沖鹽水將組織干粉浸濕,離心(3000~15000r/min)30min,除去上清液,再加入熒光抗體進行吸收,以免消耗過多的抗體。
肝粉或新鮮細胞吸收是一種非特異性的消除方法,對熒光抗體的熒光色素和蛋白都有吸附作用。如檢查組織中的病毒抗原時,也可用相同的組織干粉或勻漿沉淀物吸收之。
用臟器肝粉吸收對熒光抗體損失較多,如果根據Hiramotos氏等的方法將組織的20%生理鹽水勻漿液,用生理鹽水洗2~3次,12000r/min 10min離心沉淀,用其沉淀物吸收其熒光抗體即能*達到目的,京極方久氏認為這樣吸收對熒光抗體幾乎沒有損失,他們常用此法,效果甚佳,吸收后放置一周左右,用時有必要再吸收一次。
Second, to eliminate non-specific staining methods
Elimination of non-specific fluorescent antibody staining method should be based on the reasons for taking the appropriate method, commonly used methods are the following:
(A) animal organ powder absorption method
Commonly used liver powder (pigs, rats or mice), followed by bone marrow powder, rat brain and chicken embryo powder and so on. Add 50 ~ 100mg of liver powder per ml of fluorescent antibody, mix thoroughly in a centrifuge tube, shake at room temperature for 2h, overnight at 4 ℃, stir for 10min, centrifuge at high speed (3000 ~ 15000r / min) for 30min, After that, you can use the supernatant. Absorption generally should be carried out immediay before use, after the absorption of fluorescent antibodies stored in the refrigerator for not more than 2 weeks. Dyeing should be compared before and after absorption, the absorption can be washed with saline buffer wet tissue, centrifugation (3000 ~ 15000r / min) 30min, remove the supernatant, then add fluorescent antibodies to absorb, so as not to consume too much antibody.
Liver powder or fresh cell absorption is a nonspecific method of elimination, the fluorescence of fluorescent antibodies and proteins have adsorption. If you check the virus antigen in your tissue, you can also use the same tissue dry powder or homogenate sediment absorption.
With the organism liver powder absorption of fluorescent antibody loss more, according to Hiramotos's method of tissue 20% normal saline homogenate, washed with saline 2-3 times, 12000r / min 10min centrifugal precipitation, with its precipitate Absorption of its fluorescent antibodies that can fully achieve the purpose, Kyrgyzstan side Kyrgyzstan think this absorption of almost no loss of fluorescent antibodies, they commonly used this method, the effect is very good, after absorption for a week or so, when necessary it is necessary to absorb again.