德國Nova瘧疾
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The microplate is coated with recombinant antigens of P. falciparum and P. vivax. P. ovale and P. malaria are also detected due to the antigenic similarity between the different Plasmodium species.
- 產(chǎn)品描述
德國Nova瘧疾檢測試劑盒
瘧疾是一種危及生命的疾病,這是由原生動物引起的瘧原蟲spp。傳播是由瘧蚊傳播,但可以通過輸血也發(fā)生。人類可以通過四個(gè)不同種類的瘧原蟲感染間日瘧原蟲、惡性瘧原蟲,p .那三日瘧原蟲。
感染惡性瘧原蟲可以是致命的。惡性瘧原蟲和間日瘧原蟲是zui常見的類型。該病主要發(fā)生在熱帶和亞熱帶地區(qū)。
瘧疾感染誘發(fā)特定抗體的生產(chǎn)。一般發(fā)生后幾天內(nèi)可以檢測到血液中的寄生蟲。特定抗體的濃度成正比,感染的強(qiáng)度和持續(xù)時(shí)間。抗體的檢測比直接檢測更敏感的病原體和獨(dú)立地位的感染。*在人類感染的特定抗體水平下降后快速恢復(fù)。??比之下抗體水平下降緩慢(在2 ?3年)重新感染的人進(jìn)入非流行地區(qū)。
NovaLisa嗎?瘧疾抗體試驗(yàn)是一種快速、敏感的酶免疫分析法檢測特定的免疫球蛋白和IgM抗體瘧原蟲。
微型板塊上涂了一層重組抗原的惡性瘧原蟲和間日瘧原蟲。p .那和p .瘧疾也發(fā)現(xiàn)由于抗原不同瘧原蟲物種之間的相似性。
硬幣的瘧原蟲 | 培養(yǎng)時(shí)間 | 類型的瘧疾 | 發(fā)燒的攻擊 |
惡性瘧原蟲 | 7-30天(90%) 長(10%) | 瘧疾熱帶 | 不*的 |
三日瘧原蟲 | 16-50天 | 瘧疾Quartana | 72小時(shí) |
p .那 | 12 - 18天(90%) 長(10%) | 瘧疾Tertiana | 48小時(shí) |
間日瘧原蟲 | 12 - 180天(90%) 長(10%) | 瘧疾Tertiana | 48小時(shí) |
感染的診斷則需要通過:
顯微鏡:直接探測和識別病原體是可能的,但不確定
血清學(xué):特定抗體基于ELISA-technique的決心
NovaLisaTM瘧疾ELISA:
NovaLisaTM瘧疾ELISA用于抗體的定性測定瘧原蟲在人類血清或血漿(檸檬酸)。
主要的試驗(yàn)
定性immunoenzymatic瘧原蟲抗體的確定是基于ELISA(酶聯(lián)免疫吸附試驗(yàn))技術(shù)。
微量滴定板井重新板與瘧原蟲抗原結(jié)合相應(yīng)抗體的標(biāo)本。洗井后刪除所有的樣品材料hoseradish過氧化物酶(合)貼上人類免疫球蛋白和IgM共軛。這種共軛結(jié)合捕獲Plasmodium-specific抗體。
免疫complecx結(jié)合共軛形成可視化通過添加Tetramethylbenzidine(*)襯底,使一個(gè)藍(lán)色的反應(yīng)產(chǎn)物。這個(gè)產(chǎn)品的強(qiáng)度成正比的Plasmodium-specific標(biāo)本中的抗體。硫酸添加到停止反應(yīng)。這產(chǎn)生一個(gè)黃色端點(diǎn)的顏色。吸光度在450 nm讀取使用ELISA microwell板讀者。
重組抗原:
重組CSP和MSP1蛋白質(zhì)從間日瘧原蟲和惡性瘧原蟲
具體的性能特征:
Intraassay | Interassay | 靈敏度 | 特異性 | 協(xié)議 | ||||
n | 意思是(E) | CV % | n | 意思是(南大) | CV % | 95.9% | 97.5% (276/283) | 96.9% |
22 | 1.61 | 2.76 | 24 | 33.6 | 3.16 | |||
22 | 1.89 | 3.90 | 24 | 30.46 | 4.76 | |||
22 | 0.20 | 5.52 | 24 | 2.54 | 10.28 | |||
訂單信息:
ELISA | 的數(shù)量決定 | 產(chǎn)品編號 |
瘧疾 | 96年 | JL11601 |
【公司名稱】 廣州健侖生物科技有限公司
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【公司地址】 廣州市清華科技園創(chuàng)新基地番禺石樓鎮(zhèn)創(chuàng)啟路63號二期2幢首層
Malaria
Malaria is a life-threatening disease, which is caused by the protozoon Plasmodium spp. The transmission is mediated by the Anopheles mosquito, but can occur via blood transfusion also. Humans can be infected by four different species of Plasmodium: P. falciparum, P. vivax, P. ovale and P. malariae.
Infections with P. falciparum can be deadly. P. falciparum and P. vivax are the most common types. The disease occurs mainly in tropical and subtropical areas.
The Malaria infection induces the production of specific antibodies. In general they can be detected within some days after the occurrence of the parasites in the blood. The concentration of the specific antibodies is proportional to the intensity and duration of infection. The detection of antibodies is more sensitive than the direct detection of the pathogen and independent of the status of the infection. In humans who are infected for the first time the level of the specific antibodies decreases fast after recuperation. In contrast the antibody level decreases slowly (within 2 ? 3 years) in re-infected persons who move into non-endemic areas.
The NovaLisa? Malaria antibody assay is a fast and sensitive enzyme immunoassay for the detection of specific IgG and IgM antibodies against Plasmodium spp.
The microplate is coated with recombinant antigens of P. falciparum and P. vivax. P. ovale and P. malaria are also detected due to the antigenic similarity between the different Plasmodium species.
Specie of Plasmodium | Incubation Time | Type of Malaria | Fever Attack |
P. falciparum | 7-30 days (90%) Longer (10%) | Malaria Tropical | Inconsistent |
P. malariae | 16-50 days | Malaria Quartana | 72 hours |
P. ovale | 12-18 days (90%) Longer (10%) | Malaria Tertiana | 48 hours |
P. vivax | 12-180 days (90%) Longer (10%) | Malaria Tertiana | 48 hours |
Infections may be diagnosed by:
Microscopy: Direct detection and indentification of the pathogen is possible but uncertain
Serology: Determination of specific antibodies based on the ELISA-technique
NovaLisaTM Malaria ELISA:
The NovaLisaTM Malaria ELISA is intended for the qualitative determination of antibodies against Plasmodium in human serum or plasma (citrate).
Principal of the Assay
The qualitative immunoenzymatic determination of antibodies against Plasmodium is based on the ELISA (Enzyme-linked Immunosorbent Assay) technique.
Microtiter strip wells re pre-coated with Plasmodium antigens to bind corresponding antibodies of the specimen. After washing the wells to remove all unbound sample material hoseradish peroxidase (HRP) labeled anti-human IgG and IgM conjugate are added. This conjugate binds to the capture Plasmodium-specific antibodies.
The immune complecx formed by the bound conjugate is visualized by adding Tetramethylbenzidine (TMB) substrate, which gives a blue reaction product. The intensity of this product is proportional to the amount of Plasmodium-specific antibodies in the specimen. Sulphuric acid is added to stop the reaction. This produces a yellow endpoint color. Absorbance at 450 nm is read using an ELISA microwell plate reader.
Recombinant Antigen:
Recombinant CSP and MSP1 proteins from Plasmodium vivax and Plasmodium falciparum
Specific performance characteristics:
Intraassay | Interassay | Sensitivity | Specificity | Agreement | ||||
n | Mean (E) | CV% | n | Mean (NTU) | CV% | 95.9% | 97.5% (276/283) | 96.9% |
22 | 1.61 | 2.76 | 24 | 33.6 | 3.16 | |||
22 | 1.89 | 3.90 | 24 | 30.46 | 4.76 | |||
22 | 0.20 | 5.52 | 24 | 2.54 | 10.28 | |||
Order information:
ELISA | Number of determinations | Product number |
Malaria | 96 | MALA0620 |
