內毒素檢測&去除試劑盒
內毒素是革蘭氏陰性菌細胞壁的一部分,是生物制品一個重要的污染物,可在宿主體內導致氣相反應,如內毒素休克、組織損傷甚至死亡。FDA要求所有藥物的最終配方必須進行內毒素檢測。因此,內毒素檢測對于用于人體或動物的生物制品、藥品以及醫療設備都是非常有必要的。
金斯瑞ToxinSensor 內毒素檢測系統使用FDA批準的鱟試劑測試方法來實現快速和高度敏感的細菌內毒素檢測。鱟試劑法內毒素檢測試劑盒能定量檢測范圍廣泛的內毒素(0.01-1EU/ml)。凝膠內毒素檢測試劑盒是一種快速定性試劑盒,可以快速檢測呈陽性或陰性的結果。ToxinEraser 內毒素去除試劑盒在內毒素的去除過程中具有較高的結合能力(超過2000000EU/ml)。
*聲明:內毒素檢測試劑盒包裝瓶/包裝盒變更,點擊查看詳情說明文件。顯色法檢測試劑盒終止液組分停售,點擊查看情況說明。
ToxinSensor 內毒素檢測試劑盒
- 包含實驗所需全部試劑
- 高度線性化和可重復的結果
- 高靈敏度:0.01EU/ml
ToxinSensor 內毒素檢測試劑盒適用于內毒素體外試驗,包括用于人體或動物的生物制品、藥品以及醫療設備。
產品訂購信息
相關產品
ToxinEraser 內毒素去除系統
—高效去除樣品中的內毒素!- 高結合能力,至少2, 000, 000EU/ml (柱體積)
- 高再生能力(>90%)
- 高穩定性和高去除力:可將樣品中內毒素含量降至0.1EU/ml*
*重復使用ToxinEraser 內毒素去除樹脂,最終去除效率根據樣品不同會有所區別。
金斯瑞ToxinEraser 是一種有效的內毒素去除工具,在重復使用之后可以將樣品中內毒素水平降低至小于1EU/ mg。該試劑盒可以用于去除蛋白質、多肽、抗體或DNA樣品中的內毒素。
產品訂購信息
相關產品
選擇指導
ToxinSensor 鱟試劑檢測法試劑盒 |
ToxinSensor 凝膠檢測法試劑盒 |
ToxinSensor 一次性檢測試劑盒 |
|
---|---|---|---|
基本介紹 | 該試劑盒利用顯色鱟試驗定量檢測范圍廣泛的內毒素 | 該試劑盒基于膠凝作用原理,是一個方便的內毒素定性檢測試劑盒 | 該試劑盒用于一次性檢測內毒素含量,有不同的靈敏度可供選擇 |
應用范圍 | 準確的檢測內毒素含量 | 定性檢測內毒素 | 一次性定性檢測內毒素 |
靈敏度 | 0.01-1EU/ml | 0.25EU/ml | 0.03EU/ml-0.25EU/ml |
鱟試劑水 | 包含 | 包含 | 不包含 |
分光光度計 | 需要 | 不需要 | 不需要 |
試劑盒組分 |
即用試劑 以及無熱源的移液槍頭和試管 |
即用試劑 以及無熱源的移液槍頭和試管 |
即用試劑 不含無熱源的耗材 |
包裝 | L00350C 16次 L00350 32次 |
L00351 40次 | L00856-L00859 |
怎樣為醫療器械檢測內毒素?
為醫療器械管腔注入不含內毒素的水15毫升(如輸液裝置、透析管等),密封兩端后在37°C水浴孵育2小時,然后將水轉移至無內毒素的小瓶。使用ToxinSensor 鱟試劑檢測法試劑盒(目錄號L00350)檢測水體中的內毒素濃度,在水中的總內毒素值便可以確定。
制備標準品溶液時能否使用塑料容器?
一般而言,內毒素在塑料表面的附著比玻璃表面更強,標準的實驗室壓力蒸汽滅菌對內毒素幾乎不會有任何影響。如要使用玻璃器皿,建議在180°C過夜滅菌以破壞任何附加的內毒素分子。我們建議您僅使用新的塑料制品,并在準備標準品溶液時確認無內毒素。金斯瑞提供Toxinsensor無內毒素離心管(目錄號M01072)用于樣品處理。
標準品溶液能否重復使用?
標準品的母液是可以保存后使用的,但是不可以反復凍融。母液的保存期限請參考說明書。而不同濃度標準品的梯度稀釋液是不可以保存后使用的,因為濃度太低,效價會降低,會影響線性。所以,標準品的稀釋液建議每次實驗時新鮮制備。
如何確定最終的數據的可靠性?
首先,建議制備所需實驗試劑時在通風櫥內進行以避免污染;
對于鱟試劑檢測法試劑盒(目錄號L00350),如果樣品的OD值在標準范圍內,最終的數據可以獲得良好的線性(R≥0.98);
對于凝膠檢測法試劑盒(目錄號L00351),可以通過陰性和陽性對照,獲得可靠的結果。如果在陰性對照下得到一個陽性的結果,這表明,鱟試劑的水可能已經被污染;如果陽性對照不凝膠,需要考慮標準品的渦旋和稀釋操作以及孵育溫度是否符合要求,也可能是鱟試劑保存不當,已經失去活性。是否可以使用96孔板讀取545nm的吸光值?
鱟試劑檢測法試劑盒(L00350)為高靈敏度定量設計,不適用于96孔板;但是可以在離心管中進行實驗,在顯色后將溶液轉移至96孔板中進行讀取。
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- Kovacs-Nolan J., et al. β-1,4-mannobiose stimulates innate immune responses and induces TLR4-dependent activation of mouse macrophages but reduces severity of inflammation during endotoxemia in mice. J Nutr. 2013 Mar;143(3):384-91.
- Schepetkin IA., et al. Immunomodulatory and hemagglutinating activities of acidic polysaccharides isolated from Combretum racemosum. Int Immunopharmacol. 2013 Mar;15(3):628-37.
- Ambalavanan N., et al. Titanium oxide nanoparticle instillation induces inflammation and inhibits lung development in mice. Am J Physiol Lung Cell Mol Physiol. 2013 Feb 1;304(3):L152-61.
- Mishra B., et al. A novel antimicrobial peptide derived from modified N-terminal domain of bovine lactoferrin: design, synthesis, activity against multidrug -resistant bacteria and Candida. Biochim Biophys Acta. 2013 Feb;1828(2):677-86.
- A Mountney, et al. Sialidase, Chondroitinase Abc And Combination Therapy After Spinal Cord Contusion Injury. J Neurotrauma. 2013 Feb 1;30(3):181-90.
- Bastiaan-Net S., et al. Biochemical And Functional Characterization Of Recombinant Fungal Immunomodulatory Proteins (Rfips). Int Immunopharmacol. 2013 Jan;15(1):167-75.
- Sameera Sayeed, et al. Multifunctional Role Of Human Splunc1 In Pseudomonas Aeruginosa Infection. Infect Immun. 2013 Jan;81(1):285-91.
- K Kouakou, et al. Immunomodulatory activity of polysaccharides isolated from Alchornea cordifolia. J Ethnopharmacol. 2013 Mar 7;146(1):232-42.
- Kaliannan K., et al. Intestinal alkaline phosphatase prevents metabolic syndrome in mice. Proc Natl Acad Sci USA. 2013 Apr 23;110(17):7003-8.
- Gomez G., et al. Immunogenic and Invasive Properties of Brucella melitensis 16M Outer Membrane Protein Vaccine Candidates Identified via a Reverse Vaccinology Approach. PLOS ONE. 2013;8(3):e59751.
- Chen H., et al. In Vivo Study of Spherical Gold Nanoparticles: Inflammatory Effects and Distribution in Mice. PLOS ONE. 2013;8(2):e58208.
- Moshiri A., et al. Role of Tissue-Engineered Artificial Tendon in Healing of a Large Achilles Tendon Defect Model in Rabbits. J Am Coll Surg. 2013 Jun 29. pii: S1072-7515(13)00312-8.
- Moshiri A., et al. Effectiveness of hybridized nano- and microstructure biodegradable, biocompatible, collagen-based, three-dimensional bioimplants in repair of a large tendon-defect model in rabbits. J Tissue Eng Regen Med. 2013 May 2. doi: 10.1002/term.1740.
- Chellan B., et al. LIGHT/TNFSR14 Can Regulate Hepatic Lipase Expression by Hepatocytes Independent of T Cells and Kupffer Cells. PLoS One. 2013;8(1):e54719.
- Hao J., et al. rFliC prolongs allograft survival in association with the activation of recipient Tregs in a TLR5-dependent manner.Cell Mol Immunol. 2013 Oct 7. doi: 10.1038/cmi.2013.44.
- Sadraeian M., et al. Prevention and Inhibition of TC-1 Cell Growth in Tumor Bearing Mice by HPV16 E7 Protein in Fusion with Shiga Toxin B-Subunit from Shigella dysenteriae. Cell J. 2013 Jul;15(2):176-81.
- Tripathi A., et al. Modulation of the CXC Chemokine Receptor 4 Agonist Activity of Ubiquitin through C-Terminal Protein Modification. Biochemistry. 2013 Jun 18;52(24):4184-92.
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