沙門氏菌（L)多價抗原血清學(xué)鑒定

廣州健侖生物科技有限公司

我司長期供應(yīng)尼古丁（可替寧）檢測試劑盒，違禁品檢測試劑盒，單卡檢測，3聯(lián)卡到12聯(lián)卡，可以自由組合，根據(jù)您的需求自由組合，*，性價比高，產(chǎn)品質(zhì)量很好。

保存要求：除了有特殊說明，免疫檢測產(chǎn)品應(yīng)保存在2-8°C

產(chǎn)品規(guī)格：2ml/瓶

保質(zhì)期：2年

本試劑盒主要用于對病菌細菌進行檢測，利用快速玻片凝集檢測技術(shù)

利用快速玻片凝集和對流免疫電泳(CIE)鑒定流感嗜血桿菌

沙門氏菌（L)多價抗原血清學(xué)鑒定

沙門氏菌（L)多價抗原血清學(xué)鑒定

【沙門氏知識點】

沙門氏等在霍亂流行時分離到豬霍亂沙門氏菌，故定名為沙門氏菌屬。沙門氏菌屬有的專對人類致病，有的只對動物致病，也有對人和動物都致病。沙門氏菌病是指由各種類型沙門氏菌所引起的對人類、家畜以及野生不同形式的總稱。感染沙門氏菌的人或帶菌者的糞便污染食品，可使人發(fā)生食物中毒。據(jù)統(tǒng)計在世界各國的種類細菌性食物中毒中，沙門氏菌引起的食物中毒常列。我國內(nèi)陸地區(qū)也以沙門氏菌為*。
沙門氏菌病的病原體。屬腸桿菌科，革蘭氏陰性腸道桿菌。已發(fā)現(xiàn)的近一千種（或菌株）。按其抗原成分，可分為甲、乙、丙、丁、戊等基本菌組。其中與人體疾病有關(guān)的主要有甲組的副傷寒甲桿菌，乙組的副傷寒乙桿菌和鼠傷寒桿菌，丙組的副傷寒丙桿菌和豬霍亂桿菌，丁組的傷寒桿菌和腸炎桿菌等。除傷寒桿菌、副傷寒甲桿菌和副傷寒乙桿菌引起人類的疾病外，大多數(shù)僅能目引起家畜、鼠類和禽類等動物的疾病，但有時也可污染人類的食物而引起食物中毒。
沙門氏菌在水中不易繁殖，但可生存2-3周，冰箱中可生存3-4個月，在自然環(huán)境的糞便中可存活1-2個月。沙門氏菌zui適繁殖溫度為37℃，在20℃以上即能大量繁殖，因此，低溫儲存食品是一項重要預(yù)防措施。
沙門氏菌是一種常見的食源性致病菌。沙門氏菌鑒定的傳統(tǒng)方法主要是根據(jù)形態(tài)學(xué)特征、培養(yǎng)特征、生理生化特征、抗原特征、噬菌體特征等。

我司還有很多種血清學(xué)診斷血清、血液檢測、免疫檢測產(chǎn)品、毒素檢測、凝集檢測、酶免檢測、層析檢測、免疫熒光檢測產(chǎn)品，。

（ MOB：楊永漢）

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。

想了解更多的產(chǎn)品及服務(wù)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

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【騰訊  】 
【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

休克時機體細胞內(nèi)溶酶體增多，體積增大，吞噬體顯著增加。溶酶體內(nèi)的酶向組織內(nèi)外釋放，多在肝和腸系膜等處，引起細胞和組織自溶。因此，在休克時，測定淋巴液和血液中溶酶體酶的含量高低，可作為細胞損傷輕重度的定量指標。通常以酸性磷酸酶、β-葡萄糖醛酸酶與組織蛋白酶為指標。關(guān)于休克時溶酶體釋放的機理，有人提出是由于H降低和三羧酸循環(huán)受阻。休克時缺血缺氧，引起細胞H值的下降(約H)，酸性水解酶活化，水解溶酶體膜，zui終導(dǎo)致溶酶體膜裂解，溶酶體釋放，使細胞、組織自溶。腫瘤溶酶體與腫瘤的關(guān)系日益引起人們的關(guān)注，一般有以下幾種觀點：()致癌物質(zhì)引起細胞分裂調(diào)節(jié)機能的障阻及染色體畸變，可能與溶酶體釋放水解酶的作用有關(guān)；()某些影響溶酶體膜通透性的物質(zhì)，如巴豆油，某些去垢劑、高壓氧等，是促進致癌作用的輔助因子，也能引發(fā)細胞的異常分裂；()在核膜殘缺的情況下，核膜對核的保護喪失，溶酶體可以溶解染色質(zhì)，而引起細胞突變；()溶酶體代謝過程中的某些產(chǎn)物是腫瘤細胞增殖的物質(zhì)基礎(chǔ)；()致癌物質(zhì)進入細胞。
During shock, lysosomes increased, the volume increased, and phagosome increased significantly. Lysosomal enzymes are released inside and outside the tissues, mostly in the liver and mesenteries, causing autolysis of cells and tissues. Therefore, during shock, the levels of lysosomal enzymes in lymph and blood can be measured and used as quantitative indicators of the severity of cell damage. Acid phosphatase, β-glucuronidase, and cathepsin are commonly used as indicators. The mechanism of lysosomal release during shock has been suggested to be due to a decrease in H and a block in the tricarboxylic acid cycle. Ischemia and hypoxia during shock cause a decrease in the H value of cells (about H), activation of acid hydrolyzing enzymes, hydrolysis of lysosomal membranes, eventually leading to lysosomal membrane breakdown, release of lysosomes, and autolysis of cells and tissues. The relationship between tumor lysosomes and tumors has increasingly attracted people's attention. There are generally the following viewpoints: () carcinogens cause cell division and regulation of functional barriers and chromosomal aberrations, may be related to the role of lysosomes to release hydrolytic enzymes; ( ) Some substances that affect the permeability of lysosomal membranes, such as croton oil, certain detergents, hyperbaric oxygen, etc., are cofactors that promote carcinogenesis and can also trigger abnormal cell division; () in nuclear membrane insufficiency In the case of nuclear membranes, the protection of the nucleus is lost, and lysosomes can dissolve chromatin and cause cell mutations; () Some of the products of lysosome metabolism are the material basis for the proliferation of tumor cells; () The entry of carcinogens cell

休克時機體細胞內(nèi)溶酶體增多，體積增大，吞噬體顯著增加。溶酶體內(nèi)的酶向組織內(nèi)外釋放，多在肝和腸系膜等處，引起細胞和組織自溶。因此，在休克時，測定淋巴液和血液中溶酶體酶的含量高低，可作為細胞損傷輕重度的定量指標。通常以酸性磷酸酶、β-葡萄糖醛酸酶與組織蛋白酶為指標。關(guān)于休克時溶酶體釋放的機理，有人提出是由于H降低和三羧酸循環(huán)受阻。休克時缺血缺氧，引起細胞H值的下降(約H)，酸性水解酶活化，水解溶酶體膜，zui終導(dǎo)致溶酶體膜裂解，溶酶體釋放，使細胞、組織自溶。腫瘤溶酶體與腫瘤的關(guān)系日益引起人們的關(guān)注，一般有以下幾種觀點：()致癌物質(zhì)引起細胞分裂調(diào)節(jié)機能的障阻及染色體畸變，可能與溶酶體釋放水解酶的作用有關(guān)；()某些影響溶酶體膜通透性的物質(zhì)，如巴豆油，某些去垢劑、高壓氧等，是促進致癌作用的輔助因子，也能引發(fā)細胞的異常分裂；()在核膜殘缺的情況下，核膜對核的保護喪失，溶酶體可以溶解染色質(zhì)，而引起細胞突變；()溶酶體代謝過程中的某些產(chǎn)物是腫瘤細胞增殖的物質(zhì)基礎(chǔ)；()致癌物質(zhì)進入細胞。
During shock, lysosomes increased, the volume increased, and phagosome increased significantly. Lysosomal enzymes are released inside and outside the tissues, mostly in the liver and mesenteries, causing autolysis of cells and tissues. Therefore, during shock, the levels of lysosomal enzymes in lymph and blood can be measured and used as quantitative indicators of the severity of cell damage. Acid phosphatase, β-glucuronidase, and cathepsin are commonly used as indicators. The mechanism of lysosomal release during shock has been suggested to be due to a decrease in H and a block in the tricarboxylic acid cycle. Ischemia and hypoxia during shock cause a decrease in the H value of cells (about H), activation of acid hydrolyzing enzymes, hydrolysis of lysosomal membranes, eventually leading to lysosomal membrane breakdown, release of lysosomes, and autolysis of cells and tissues. The relationship between tumor lysosomes and tumors has increasingly attracted people's attention. There are generally the following viewpoints: () carcinogens cause cell division and regulation of functional barriers and chromosomal aberrations, may be related to the role of lysosomes to release hydrolytic enzymes; ( ) Some substances that affect the permeability of lysosomal membranes, such as croton oil, certain detergents, hyperbaric oxygen, etc., are cofactors that promote carcinogenesis and can also trigger abnormal cell division; () in nuclear membrane insufficiency In the case of nuclear membranes, the protection of the nucleus is lost, and lysosomes can dissolve chromatin and cause cell mutations; () Some of the products of lysosome metabolism are the material basis for the proliferation of tumor cells; () The entry of carcinogens cell

休克時機體細胞內(nèi)溶酶體增多，體積增大，吞噬體顯著增加。溶酶體內(nèi)的酶向組織內(nèi)外釋放，多在肝和腸系膜等處，引起細胞和組織自溶。因此，在休克時，測定淋巴液和血液中溶酶體酶的含量高低，可作為細胞損傷輕重度的定量指標。通常以酸性磷酸酶、β-葡萄糖醛酸酶與組織蛋白酶為指標。關(guān)于休克時溶酶體釋放的機理，有人提出是由于H降低和三羧酸循環(huán)受阻。休克時缺血缺氧，引起細胞H值的下降(約H)，酸性水解酶活化，水解溶酶體膜，zui終導(dǎo)致溶酶體膜裂解，溶酶體釋放，使細胞、組織自溶。腫瘤溶酶體與腫瘤的關(guān)系日益引起人們的關(guān)注，一般有以下幾種觀點：()致癌物質(zhì)引起細胞分裂調(diào)節(jié)機能的障阻及染色體畸變，可能與溶酶體釋放水解酶的作用有關(guān)；()某些影響溶酶體膜通透性的物質(zhì)，如巴豆油，某些去垢劑、高壓氧等，是促進致癌作用的輔助因子，也能引發(fā)細胞的異常分裂；()在核膜殘缺的情況下，核膜對核的保護喪失，溶酶體可以溶解染色質(zhì)，而引起細胞突變；()溶酶體代謝過程中的某些產(chǎn)物是腫瘤細胞增殖的物質(zhì)基礎(chǔ)；()致癌物質(zhì)進入細胞。
During shock, lysosomes increased, the volume increased, and phagosome increased significantly. Lysosomal enzymes are released inside and outside the tissues, mostly in the liver and mesenteries, causing autolysis of cells and tissues. Therefore, during shock, the levels of lysosomal enzymes in lymph and blood can be measured and used as quantitative indicators of the severity of cell damage. Acid phosphatase, β-glucuronidase, and cathepsin are commonly used as indicators. The mechanism of lysosomal release during shock has been suggested to be due to a decrease in H and a block in the tricarboxylic acid cycle. Ischemia and hypoxia during shock cause a decrease in the H value of cells (about H), activation of acid hydrolyzing enzymes, hydrolysis of lysosomal membranes, eventually leading to lysosomal membrane breakdown, release of lysosomes, and autolysis of cells and tissues. The relationship between tumor lysosomes and tumors has increasingly attracted people's attention. There are generally the following viewpoints: () carcinogens cause cell division and regulation of functional barriers and chromosomal aberrations, may be related to the role of lysosomes to release hydrolytic enzymes; ( ) Some substances that affect the permeability of lysosomal membranes, such as croton oil, certain detergents, hyperbaric oxygen, etc., are cofactors that promote carcinogenesis and can also trigger abnormal cell division; () in nuclear membrane insufficiency In the case of nuclear membranes, the protection of the nucleus is lost, and lysosomes can dissolve chromatin and cause cell mutations; () Some of the products of lysosome metabolism are the material basis for the proliferation of tumor cells; () The entry of carcinogens cell

休克時機體細胞內(nèi)溶酶體增多，體積增大，吞噬體顯著增加。溶酶體內(nèi)的酶向組織內(nèi)外釋放，多在肝和腸系膜等處，引起細胞和組織自溶。因此，在休克時，測定淋巴液和血液中溶酶體酶的含量高低，可作為細胞損傷輕重度的定量指標。通常以酸性磷酸酶、β-葡萄糖醛酸酶與組織蛋白酶為指標。關(guān)于休克時溶酶體釋放的機理，有人提出是由于H降低和三羧酸循環(huán)受阻。休克時缺血缺氧，引起細胞H值的下降(約H)，酸性水解酶活化，水解溶酶體膜，zui終導(dǎo)致溶酶體膜裂解，溶酶體釋放，使細胞、組織自溶。腫瘤溶酶體與腫瘤的關(guān)系日益引起人們的關(guān)注，一般有以下幾種觀點：()致癌物質(zhì)引起細胞分裂調(diào)節(jié)機能的障阻及染色體畸變，可能與溶酶體釋放水解酶的作用有關(guān)；()某些影響溶酶體膜通透性的物質(zhì)，如巴豆油，某些去垢劑、高壓氧等，是促進致癌作用的輔助因子，也能引發(fā)細胞的異常分裂；()在核膜殘缺的情況下，核膜對核的保護喪失，溶酶體可以溶解染色質(zhì)，而引起細胞突變；()溶酶體代謝過程中的某些產(chǎn)物是腫瘤細胞增殖的物質(zhì)基礎(chǔ)；()致癌物質(zhì)進入細胞。
During shock, lysosomes increased, the volume increased, and phagosome increased significantly. Lysosomal enzymes are released inside and outside the tissues, mostly in the liver and mesenteries, causing autolysis of cells and tissues. Therefore, during shock, the levels of lysosomal enzymes in lymph and blood can be measured and used as quantitative indicators of the severity of cell damage. Acid phosphatase, β-glucuronidase, and cathepsin are commonly used as indicators. The mechanism of lysosomal release during shock has been suggested to be due to a decrease in H and a block in the tricarboxylic acid cycle. Ischemia and hypoxia during shock cause a decrease in the H value of cells (about H), activation of acid hydrolyzing enzymes, hydrolysis of lysosomal membranes, eventually leading to lysosomal membrane breakdown, release of lysosomes, and autolysis of cells and tissues. The relationship between tumor lysosomes and tumors has increasingly attracted people's attention. There are generally the following viewpoints: () carcinogens cause cell division and regulation of functional barriers and chromosomal aberrations, may be related to the role of lysosomes to release hydrolytic enzymes; ( ) Some substances that affect the permeability of lysosomal membranes, such as croton oil, certain detergents, hyperbaric oxygen, etc., are cofactors that promote carcinogenesis and can also trigger abnormal cell division; () in nuclear membrane insufficiency In the case of nuclear membranes, the protection of the nucleus is lost, and lysosomes can dissolve chromatin and cause cell mutations; () Some of the products of lysosome metabolism are the material basis for the proliferation of tumor cells; () The entry of carcinogens cell