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BioAssay Systems/QuantiChrom™ Calcium Assay Kit/500 tests/DICA-500
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BioAssay Systems/QuantiChrom™ Calcium Assay Kit/500 tests/DICA-500
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BioAssay Systems
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DICA-500
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QuantiChrom™ Calcium Assay Kit

QuantiChrom™ Calcium Assay Kit Catalog No: DICA-500
Price: $329 Qty:
For orders of 10 or more kits, please call +1-510-782-9988x1 oremail us for best pricing and/or bulk order. Shipping: RT Shipment: Fedex ServiceDelivery: 1-2 days (US), 3-6 days (Intl) Storage: 4°C
Calcium Assay Kit
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ProtocolSDS

Application

  • For quantitative determination of calcium ion Ca2+ and evaluation of drug effects on calcium metabolism.

Key Features

  • Sensitive and accurate. Use as little as 5 μL samples. Linear detection range 0.08 mg/dL (20 μM) to 20 mg/dL (5 mM) Ca2+ in 96-well plate assay.
  • Simple and high-throughput. The procedure involves addition of a single working reagent and incubation for 3 min. Can be readily automated as a high-throughput assay for thousands of samples per day.
  • Improved reagent stability and versatility. The optimized formulation has greatly enhanced reagent and signal stability. Cuvet or 96-well plate assay.
  • Low interference in biological samples. No pretreatments are needed. Assays can be directly performed on raw biological samples i.e., in the presence of lipid, protein and minerals such as magnesium, iron and zinc.

Method

  • OD612nm

Samples

  • Biological, food and environment

Species

  • All

Size

  • 500 tests

Detection Limit

  • 0.08 mg/dL (20 μM)

Shelf Life

  • 12 months

More Details

  • CALCIUM is measured to monitor diseases of the bone or calcium regulation disorders. Increased calcium levels in serum are reported in hyperparathyroidism, metastatic bone lesions and hypervitaminosis, while decreased levels are observed in hypoparathyroidism, nephrosis, rickets, steatorrhea, nephritis and calcium-losing syndromes. Urinary calcium levels aid the clinician in understanding how the kidneys handle calcium in certain diseases of the parathyroid gland. Urinary calcium levels are also essential in the medical evaluation of kidney stones. Simple, direct and automation-ready procedures for measuring calcium concentration in biological samples are becoming popular in Research and Drug Discovery. BioAssay Systems calcium assay kit is designed to measure calcium directly in biological samples without any pretreatment. A phenolsulphonephthalein dye in the kit forms a very stable blue colored complex specifically with free calcium. The intensity of the color, measured at 612 nm, is directly proportional to the calcium concentration in the sample. The optimized formulation minimizes any interference by substances such as magnesium, lipid, protein and bilirubin.

We have whole blood samples. Does your assay work?

Yes, our QuantiChromTM Calcium Assay Kit (DICA-500) can be used on whole blood samples. To correct for interference in the sample matrix, two internal standard methods have been validated. Protocol A is quicker whereas Protocol B is slightly more involved, but requires less sample and is, thus, recommended for customer"s that have a limited quantity of sample. Additionally, protocol B requires less Reagent because each sample requires one well rather than three separate wells per sample. Please note that 20 mM EDTA is needed for this experiment and is not provided. The customer should prepare this solution, or is available for purchase upon request. PROTOCOL A: 3 Separate wells needed for each sample A1. Whole Blood samples require an internal standard and need three separate reactions: 1) Sample plus Standard 2) Sample alone and 3) Sample Blank. For the internal standard prepare 250 µL 10 mg/dL Ca2+ Standard by mixing 125 µL 20 mg/dL Standard and 125 µL dH2O.Transfer 5 µL whole blood sample to three separate wells. Add 5 µL of 10 mg/dL Ca2+ to the 1) Sample plus Standard well, 5 µL dH2O to 2) Sample alone well and 5 µL 20 mM EDTA to 3) sample Blank well.A2. Add 200 µL Working Reagent and tap lightly to mix. Note: If any particulates or turbidity are seen pipette up and down to dissolve.A3. Incubate 3 min at room temperature and read optical density at 570-650 nm (peak absorbance at 612 nm).PROTOCOL B: 1 Well needed for each sample B1. Dilute standard to 10 mg/dL Ca2+ by mixing 125 µL 20 mg/dL Standard and 125 µL dH2O.B2. Transfer 5 µL whole blood sample to a well.B3. Add 200 µL Working Reagent and tap lightly to mix. Note: If any particulates are seen pipette up and down to dissolve.B4. Incubate 3 min at room temperature and read optical density at 570-650 nm (peak absorbance at 612 nm). ODSAMPLE B5. Carefully transfer 5 µL of 10 mg/dL standard to the sample well from step 2. Tap plate to mix. Repeat Step 4. ODSTANDARD B6. Add 5 µL of 20 mM EDTA to the same well from step 2. Tap plate to mix. Repeat step 4. ODBLANK CALCULATIONThe whole blood sample concentration is computed as follows:[Ca2+] = (ODSAMPLE - ODBLANK)/(ODSTANDARD - ODSAMPLE) x 10 x n (mg/dL)where ODSAMPLE, ODBLANK, and ODSTANDARD are the OD readings of the Sample, Sample Blank, and the Sample plus Standard respectively, 10 is the concentration of the standard in mg/dL, and n is the sample dilution factor. If the calculated calcium concentration is greater than 10 mg/dL, dilute sample in dH2O and repeat assay. Multiply result by the dilution factor n.EXAMPLE One human blood sample was assayed using the two methods. The Ca2+ concentration was 8.48 mg/dL using Protocol A and 8.38 mg/dL using Protocol B.

Is the calcium assay compatible with acids?

Yes, our QuantiChromTM Calcium Assay is compatible with acids, such as 0.5 M HCl.

Do you know if phosphate in the sample will interfere with the calcium assay or if calcium in the sample will interfere with the phosphate assay?

Phosphate (at least up to 30 mM) in the sample does not interfere with the calcium assay.

Does freezing of serum have any impact on serum Ca compared to using fresh serum?

Our assay kit measures the total calcium content of samples. In serum about half of the calcium is free ("ionized") and the other half is bound to proteins, especially albumin (~40%) or anions (~10%). Repeated freeze-thaw cycles may cause precipitation of proteins which would alter the outcome of the assay. We recommend avoiding repeated freeze thaw cycles for serum samples.For more detailed product information and questions, please feel free to Contact Us. Or for more general information regarding our assays, please refer to our General Questions.
Cruz, A.C.C. et al (2019). Retinoic acid increases the effect of bone morphogenetic protein type 2 on osteogenic differentiation of human adipose-derived stem cells. Journal of Applied Oral Science 27:e20180317. Assay: Calcium in human mesenchymal stem cells. Li, Y., et al. (2019). Biofunctionalization of decellularized porcine aortic valve with OPG-loaded PCL nanoparticles for anti-calcification. RSC advances, 9(21), 11882-11893. Assay: Calcium in rats bone marrow.Schanstra, J. P.et al. (2019). Systems biology identifies cytosolic PLA2 as a target in vascular calcification treatment. JCI insight, 4(10) pii: 125638. Assay: Calcium in human plasma. Schelski, N., Luong, T. T., Lang, F., Pieske, B., Voelkl, J., & Alesutan, I. (2019). SGK1-dependent stimulation of vascular smooth muscle cell osteo-/chondrogenic transdifferentiation by interleukin-18. Pflugers Archiv-European Journal of Physiology, 471(6):889-899. Assay: Calcium in human aortic smooth muscle cells. Tsolaki, E., Didierlaurent, L., Muller, E., Rottmar, M., Latif, N., Chester, A. H. & Bertazzo, S. (2019). Electron microscopy characterization of minerals formed in vitro by human bone cells and vascular smooth muscle cells. BioRxiv, 661785. Assay: Calcium in human bone cells.Bora, S. A., Kennett, M. J., Smith, P. B., Patterson, A. D., & Cantorna, M. T. (2018). The gut microbiota regulates endocrine vitamin D metabolism through fibroblast growth factor 23. Frontiers in immunology, 9, 408. Assay: Calcium in mice cells. Bouyoucos, I. A., Talwar, B. S., Brooks, E. J., Brownscombe, J. W., Cooke, S. J., Suski, C. D., & Mandelman, J. W. (2018). Exercise intensity while hooked is associated with physiological status of longline-captured sharks. Conservation physiology, 6(1), coy074. Assay: Calcium in shark plasma calcium. Gurel Pekozer, G., Ramazanoglu, M., Schlegel, K. A., Kok, F. N., & Torun Kose, G. (2018). Role of STRO-1 sorting of porcine dental germ stem cells in dental stem cell-mediated bone tissue engineering. Artificial cells, nanomedicine, and biotechnology, 46(3), 607-618. Assay: Calcium in porcine teeth. Kagi, L., Bettoni, C., Pastor-Arroyo, E. M., Schnitzbauer, U., Hernando, N., & Wagner, C. A. (2018). Regulation of vitamin D metabolizing enzymes in murine renal and extrarenal tissues by dietary phosphate, FGF23, and 1, 25 (OH) 2D3. PloS one, 13(5), e0195427. Assay: Calcium in mice spot urine. Ma, G. T., Lee, S. K., Park, K. K., Park, J., Son, S. H., Jung, M., & Chung, W. Y. (2018). Artemisinin-Daumone Hybrid Inhibits Cancer Cell-Mediated Osteolysis by Targeting Cancer Cells and Osteoclasts. Cellular Physiology and Biochemistry, 49(4), 1460-1475. Assay: Calcium in mice serum. Onal, M., Carlson, A. H., Thostenson, J. D., Benkusky, N. A., Meyer, M. B., Lee, S. M., & Pike, J. W. (2018). A Novel Distal Enhancer Mediates Inflammation-, PTH-, and Early Onset Murine Kidney Disease-Induced Expression of the mouse Fgf23 Gene. JBMR plus, 2(1), 31-46. Assay: Calcium in mice maxillary blood.Roh, J. Y., & Kim, K. R. (2018). Anti-inflammatory effect of new calcium hydroxide paste containing silicon-substituted hydroxyapatite in lipopolysaccharide-stimulated macrophages. J Korean Soc Dent Hyg 18(4), 423-432. Assay: Calcium in plant. Townsend, J. M., Zabel, T. A., Feng, Y., Wang, J., Andrews, B. T., Nudo, R. J. & Detamore, M. S. (2018). Effects of tissue processing on bioactivity of cartilage matrix-based hydrogels encapsulating osteoconductive particles. Biomedical Materials, 13(3), 034108. Assay: Calcium in rats bone marrow. Vollersen, N., Hermans-Borgmeyer, I., Cornils, K., Fehse, B., Rolvien, T., Triviai, I. & Yorgan, T. A. (2018). High Bone Turnover in Mice Carrying a Pathogenic Notch2 Mutation Causing Hajdu-Cheney Syndrome. Journal of Bone and Mineral Research, 33(1), 70-83. Assay: Calcium in mice serum. Aimaiti, A., Maimaitiyiming, A., Boyong, X., Aji, K., Li, C., & Cui, L. (2017). Low-dose strontium stimulates osteogenesis but high-dose doses cause apoptosis in human adipose-derived stem cells via regulation of the ERK1/2 signaling pathway. Stem cell research & therapy, 8(1), 282. Assay: Calcium in human bone marrow. BARINDA, A. J., Ikeda, K., Hirata, K. I., & Emoto, N. (2017). Macrophages Highly Express Carbonic Anhydrase 2 and Play a Significant Role in Demineralization of the Ectopic Calcification. Kobe Journal of Medical Sciences, 63(2), E45. Assay: Calcium in culture plate fibronectin. Go, Y. Y., Kim, S. E., Cho, G. J., Chae, S. W., & Song, J. J. (2017). Differential effects of amnion and chorion membrane extracts on osteoblast-like cells due to the different growth factor composition of the extracts. PloS one, 12(8), e0182716. Assay: Calcium in human amniotic membrane. Hu, K., Sun, H., Gui, B., & Sui, C. (2017). Gremlin-1 suppression increases BMP-2-induced osteogenesis of human mesenchymal stem cells. Molecular medicine reports, 15(4), 2186-2194. Assay: Calcium in human bone marrow. Kim, E. C., Park, J., Kwon, I. K., Lee, S. W., Park, S. J., & Ahn, S. J. (2017). Static magnetic fields promote osteoblastic/cementoblastic differentiation in osteoblasts, cementoblasts, and periodontal ligament cells. Journal of periodontal & implant science, 47(5), 273-291. Assay: Calcium in human fetal osteoblast. Paul, S., Gangwar, A., Bhargava, K., & Ahmad, Y. (2017). Deciphering Molecular Cascades In A Novel Acclimatization Strategy For Rapid Ascent To High Altitude. bioRxiv, 145342. Assay: Calcium in Sprague Dewley rats lung tissue/plasma.Vanacker, N., Ollier, S., Beaudoin, F., Blouin, R., & Lacasse, P. (2017). Effect of inhibiting the lactogenic signal at calving on milk production and metabolic and immune perturbations in dairy cows. Journal of dairy science, 100(7), 5782-5791. Assay: Calcium in Holstein Cows serum. Wang, F., Johnson, R. L., DeSmet, M. L., Snyder, P. W., Fairfax, K. C., & Fleet, J. C. (2017). Vitamin D Receptor-Dependent Signaling Protects Mice From Dextran Sulfate Sodium-Induced Colitis. Endocrinology, 158(6), 1951-1963. Assay: Calcium in mice intestinal cells. Birgani, Z. T., van Blitterswijk, C. A., & Habibovic, P. (2016). Monolithic calcium phosphate/poly (lactic acid) composite versus calcium phosphate-coated poly (lactic acid) for support of osteogenic differentiation of human mesenchymal stromal cells. Journal of Materials Science: Materials in Medicine, 27(3), 54. Assay: Calcium in monolithic PLA/CaP composite. Cai, T., Sun, D., Duan, Y., Wen, P., Dai, C., Yang, J., & He, W. (2016). WNT/beta-catenin signaling promotes VSMCs to osteogenic transdifferentiation and calcification through directly modulating Runx2 gene expression. Experimental cell research, 345(2), 206-217. Assay: Calcium in rats smooth muscles. Corcoran, A., Bermudez, M. A., Seoane, S., Perez-Fernandez, R., Krupa, M., Pietraszek, A. & Marcinkowska, E. (2016). Biological evaluation of new vitamin D2 analogues. The Journal of steroid biochemistry and molecular biology, 164, 66-71. Assay: Calcium in mice serum. Go, Y. Y., Kim, S. E., Cho, G. J., Chae, S. W., & Song, J. J. (2016). Promotion of osteogenic differentiation by amnion/chorion membrane extracts. Journal of applied biomaterials & functional materials, 14(2), 171-180. Assay: Calcium in human amniotic membrane. Kim, W., et al. (2016). Calcium-sensing receptor promotes breast cancer by stimulating intracrine actions of parathyroid hormone-related protein. Cancer research, 76(18), 5348-5360. Assay: Calcium in mice serum. Kose, S et al (2016). Evaluation of biocompatibility of random or aligned electrospun polyhydroxybutyrate scaffolds combined with human mesenchymal stem cells. Turkish Journal of Biology, 40(2), 410-419. Assay: Calcium in human myscenchymal cells.Mao, J., Shi, X., Wu, Y. B., & Gong, S. Q. (2016). Identification of specific hydroxyapatite {001} binding heptapeptide by phage display and its nucleation effect. Materials, 9(8), 700. Assay: Calcium in human teeth. Onal, M., St. John, H. C., Danielson, A. L., & Pike, J. W. (2016). Deletion of the distal Tnfsf11 RL-D2 enhancer that contributes to PTH-mediated RANKL expression in osteoblast lineage cells results in a high bone mass phenotype in mice. Journal of Bone and Mineral Research, 31(2), 416-429. Assay: Calcium in mice osteoblast cells. Villa-Bellosta, R., Gonzalez-Parra, E., & Egido, J. (2016). Alkalosis and dialytic clearance of phosphate increases phosphatase activity: a hidden consequence of hemodialysis. PloS one, 11(7), e0159858. Assay: Calcium in human plasma. Villa-Bellosta, R., Hamczyk, M. R., & Andres, V. (2016). Alternatively activated macrophages exhibit an anticalcifying activity dependent on extracellular ATP/pyrophosphate metabolism. American Journal of Physiology-Cell Physiology, 310(10), C788-C799. Assay: Calcium in mice smooth muscles. Ballester-Lozano GF et al. (2015). Comprehensive biometric, biochemical and histopathological assessment of nutrient deficiencies in gilthead sea bream fed semi-purified diets. Br J Nutr. 114(5):713-26. Assay: calcium in fish plasma. Chaumet-Riffaud P, et al (2010). Synthesis and application of lactosylated, 99mTc chelating albumin for measurement of liver function. Bioconjug Chem. 21(4):589-96. Assay: Calcium in mice liver tissue. Jung GY, et al (2010). Effects of HA released calcium ion on osteoblast differentiation. J Mater Sci Mater Med. 21(5):1649-54. Assay: Calcium in mouse 3T3 cell. Ou KL, et al (2010). Effects of the nanostructure and nanoporosity on bioactive nanohydroxyapatite/reconstituted collagen by electrodeposition. J Biomed Mater Res A. 92(3):906-12. Assay: Calcium in human stem cell. Ponda MP,et al (2010). Moderate kidney disease inhibits atherosclerosis regression. Atherosclerosis.210(1):57-62. Assay: Calcium in mice serum. Zarjou A, et al (2010). Ferritin ferroxidase activity: a potent inhibitor of osteogenesis. J Bone Miner Res. 25(1):164-72. Assay: Calcium in human osteoblasts cell. Brand A, et al (2009). Calcium homeostasis is required for contact-dependent helical and sinusoidal tip growth in Candida albicans hyphae. Mol Microbiol. 71(5):1155-64. Assay: Calcium in cattle FBS. Koreckij T, et al (2009). Dasatinib inhibits the growth of prostate cancer in bone and provides additional protection from osteolysis. Br J Cancer.101(2):263-8. Assay: Calcium in mice serum. Villa-Bellosta R, Sorribas V (2009). Phosphonoformic acid prevents vascular smooth muscle cell calcification by inhibiting calcium-phosphate deposition. Arterioscler Thromb Vasc Biol. 29(5):761-6. Assay: Calcium in rat muscle cell. Chanda, D et al (2008). Systemic osteoprotegerin gene therapy restores tumor-induced bone loss in a therapeutic model of breast cancer bone metastasis. Mol Ther. 16(5):871-8. Assay: Calcium in mouse serum. He X, et al (2008). Effect of grafting RGD and BMP-2 protein-derived peptides to a hydrogel substrate on osteogenic differentiation of marrow stromal cells. Langmuir. 24(21):12508-16. Assay: Calcium in human marrow cell. Henderson JA, et al (2008). Concurrent differentiation of marrow stromal cells to osteogenic and vasculogenic lineages. Macromol Biosci. 8(6):499-507. Assay: Calcium in human marrow cell. Warotayanont R, et al (2008). Leucine-rich amelogenin peptide induces osteogenesis in mouse embryonic stem cells. Biochem Biophys Res Commun. 367(1):1-6. Assay: Calcium in mouse stem cell.To find more recent publications, pleaseclick here.
If you or your labs do not have the equipment or scientists necessary to run this assay, BioAssay Systems can perform the service for you.Simply send us your samples:- Fast turnaround - Quality data - Low costPlease email or call 1-510-782-9988 x 2 to request assay service.
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 PE标记的兔抗猴IgG兔抗猴IgG / PE猫。量大小:0.1ml浓度为1mg/ml缓冲= 0.01m TBS(pH7.4)1%牛血清白蛋白,0.03% proclin300和50%甘油。背景:Immunoglobulin G(IgG),是一个最丰富的蛋白质,与正常血清8-17毫克/毫升之间血。IgG对我们防御微生物很重要,而分子是由B淋巴细胞产生的,作为我们适应性免疫反应的一部分。IgG分子有两个独立的功能:与引起反应的病原体结合,并招募 查看更多>
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疾病才是治疗的目标狼疮的起源狼疮(Lupus)这一术语最早始于中世纪,它主要是用来与“被狼咬过后的皮肤损伤相似”的糜烂性皮肤改变。而古典时期的红斑狼疮始于 1846 年。当时维也纳医师 von Hebra 描述了面颊部的“蝴蝶样”红斑改变,他也曾用“红斑狼疮”一词来描述该病。此后医学大家 Kaposi 根据尸体解剖第一个提出红斑狼疮是一个全身性疾病。这一观点被伟大的 Willia 查看更多>
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如题,哪几家做定制猴抗体服务比较好的?

谢谢

求牛人推荐好一点的抗食蟹猴的干扰素gamma的抗体,做猴体Elispot用,最好能配上文献证明和生产厂家,谢谢。本人小白,没有悬赏,不好意思。

日期:2016-04-28信息来源:分子医学研究所


北京大学分子医学研究所利用非人灵长类动物模型,发现盐皮质激素受体阻断剂可以治疗高血压伴随的血压昼夜节律紊乱,提出高血压治疗的新机制和新的药物评价指标。

高血压是临床上最多见的心血管疾病之一,常伴有包括心、脑、肾等多种器官的功能或器质性损害,严重威胁人类健康。血压的调控具有明显的昼夜节律,动脉血压一般在夜间入睡后降低10-20%,清晨迅速回升,而高血压患者血压的昼夜节律紊乱,尤其是夜间血压降低的幅度明显减小。临床证据表明,血压昼夜节律紊乱与病人心血管事件的发生率和死亡率密切相关,因此,恢复血压昼夜节律对高血压的治疗及预防其并发症的发生具有重要的意义。

自2006年以来,北京大学分子医学研究所非人灵长类研究中心利用恒河猴建立了多种代谢性和心血管疾病模型。本研究首次建立了自发性代谢综合征高血压恒河猴模型,而后利用手术植入血压无线遥测系统,对恒河猴的24小时血压进行长达数月的实时连续测量。结果发现,自发性代谢综合征高血压恒河猴模型不仅血压升高,而且夜间血压降低的幅度也显著变小。利用一线临床抗高血压药物伊普利酮(eplerenone),不仅降低了血压,而且明显恢复了夜间血压降低的幅度,改善了血压昼夜节律的紊乱。同时伊普利酮还降低了血液中炎症因子和糖基化终末产物的浓度。

本研究首次在灵长类动物模型上证明了改善紊乱的昼夜血压节律也是伊普利酮治疗高血压、保护心血管系统的重要因素,同时发现了新的伊普利酮的作用机制。自发性代谢综合征高血压非人灵长类动物模型的建立,为临床高血压发病机制和药物治疗研究提供了非常重要的动物模型:与常用的啮齿类动物模型相比,非人灵长类动物模型在药物代谢、心血管疾病的发生和遗传等方面与人类更加类似;而与人类相比,该模型又具有不受药物和生活方式的干扰、研究条件可控性强等优势。

该工作于近日在线发表于ScientificReports杂志(http://www.ncbi.nlm.nih.gov/pubmed/?term=27032687)。张岩副研究员是本文的第一作者;张秀琴研究员和肖瑞平教授为文章的共同通讯作者。该项研究得到国家自然科学基金委、科技部“973”项目、科技部国家科技重大专项、北大-清华生命科学联合中心、生物膜与膜生物国家重点实验室、北京市重点实验室和默沙东公司的支持。


A图为伊普利酮治疗前后血压的昼夜变化B图为伊普利酮的功效



在一篇文献给里看到“双抗夹心ELISA法”方法是这样描述的:采用双抗夹心ELISA法对重组抗CD20单克隆抗体进行定量检测,包被抗体用猴血清吸附的羊抗人IgG,检测抗体用猴血清吸附的羊抗人IgG—HRP,最后加底物显色剂,终止后在酶标仪450nm下读数。想请问这个用“猴血清吸附”是怎样的处理过程呢?因我没有做过此类实验,故请求解答。谢谢!

往常一直用“猴年马月”来形容时间的漫长,来看看我们身边与“猴”相关的药物物种都有哪些呢?您最熟悉的是什么?


今天逛超市,印象最深的是据说有“抗癌”作用的猴头菌,来看看它的功效有哪些


《全国中草药汇编》:猴头菌


【药材名称】猴头菌


【别名】猴头、刺猬菌、猬菌


【来源】真菌类担子菌纲多孔菌目齿菌科猴头菌Hericiumerinaceus(Bull.exFr.)Pers.,以子实体入药。


【生境分部】生于栎、胡桃等阔叶树种的立木及腐木上。


【性味】甘,平。


【功能主治】利五脏,助消化。主治消化不良,神经衰弱、身体虚弱。


【用法用量】消化不良:猴头菌2两,水浸软,切成薄片,水煎服,日服2次,黄酒为引。


神经衰弱、身体虚弱:猴头菌(干品)5两,切片与鸡共煮食用,日服1次(或用鸡汤煮食)。


【备注】(1)据文献,本品子实体内含抗癌物质。


(2)还有一种小刺猴头菌Herieiumcaptmedusae(Bull.exFr.)Pers.,刺密而短,效用同猴头菌。


【摘录】《全国中草药汇编》


下面是《中华本草》的记载:


【药理作用】1.增强免疫功能
同基因骨髓移植55d后,受体小鼠免疫功能严重损害。脾细胞产生白介素-2(IL-2)能力等细胞免疫功能明显低下,连续腹腔注射猴头菌多糖和胸腺肽15d后,小鼠脾细胞产生IL-2能力及对刀豆素A(Con
A)刺激的增殖反应和混合淋巴细胞培养反应,均显着增强。说明猴头菌多糖与胸腺肽合用比单独使用胸腺肽更能明显促进同基因骨髓移植小鼠免疫功能的早期恢复。猴头菌多糖给小鼠腹腔注射2mg/只,连续7d,能明显提高小鼠腹腔巨噬细胞的吞噬功能;可促进溶血素生成,增加体液免疫的能力。若给小鼠腹腔注射2.88mg/只,连续8d,则可明显对抗由环磷酰胺中毒所引起的白细胞下降,下降率仅为对照组的一半。猴头菌多糖在体外对由ConA活化的小鼠胸腺细胞有较强的促进增殖作用,也可促进脾淋巴细胞的增殖,并对脂多糖(LPS)刺激的B细胞也有协同作用。


2.抑瘤作用在Swiss雄性小鼠左前腋皮下,接种肉瘤S180细胞,然后口服猴头菌多糖50mg/kg,100mg/kg,200mg/kg,每日1次,连续7d,结果表明,3个剂量组对荷瘤生长均有抑制作用;对自然杀伤(NK)细胞活性有明显的激活作用;荷瘤重量与其相应鼠脾NK细胞活性呈负相关猴头菌还能抑制黄曲霉素对大鼠的致肝癌作用,减少肝切面的病灶数。


3.抗溃疡作用及降血糖作用通过胃蛋白酶抑制吸附实验,证明猴菇菌片治疗胃溃疡的作用机制,可能是由于抑制胃蛋白酶活性而促进溃疡愈合。猴头菌多糖可降低小鼠正常血糖和四氢嘧啶所致糖尿病小鼠的血糖水平。


4.延缓衰老作用猴头菌丝体多糖和子实体多糖能显着增加果蝇飞翔能力,降低刚孵化果蝇和小鼠心肌组织脂褐质含量,并能增加小鼠脑和肝脏中超氧化物歧化酶(SOD)的比活力。


【性味】甘;平


【归经】入脾、胃经


【功能主治】健脾养胃;安神;抗癌。主体虚乏力;消化不良;失眠;胃与十二指肠溃疡;慢性胃炎;消化道肿瘤


【用法用量】内服:煎汤,10~30g,鲜品30~100g;或与鸡共煮食。


【各家论述】1.《临海水土异物志》:民皆好啖猴头羹,虽五肉臛不能及之,其俗言:宁负千石之粟,不愿负猴头羹CONG。


2.《农政全书》:如无花、麻姑、猴头之属,皆草木根腐坏而成者。


3.《新华本草纲要》:全草:味甘,性平。有利五脏、助消化、滋补、抗癌等功能。与本品有类似功效,且分布区相近似的尚有以下两个近缘种:玉髯
H.Coralloides(Scop.Fr.)Pers,exGtay及分枝猴头菌H.ramosum(Bull.Ex
Merat。)Letellier.


找了张照片,猴头菇哦




各位兄弟姐妹,大家可知哪个公司可以买到抗猴CD8和CD3荧光标记单抗
如果没有抗猴CD8单抗,哪种克隆的人CD8单抗和猴的有交叉反应,可以拿来检测猴CD8T细胞。

多谢了
美国科学家宣布重大发现猴蛋白能抗艾滋病毒
中新网2月26日电据美联社报道,科学家称已经***了猴子抵抗艾滋病毒感染的机密。这是一个让人欣喜的重大发现,因为接下来的研究很可能发现一个人类预防艾滋病的新策略。

  某些灵长目动物可以防止艾滋病菌在体内蔓延,这一谜团困扰科学家长达10年之久,如今终于有了答案。

  美国健康研究所基础科学研究室主任称,人们根据这一发现可能研制出治疗爱滋的药物,或者是预防爱滋的疫苗。“我们将立即就15个不同方向进行研究。这将是基础研究意义重大的一年,我们取得了很多的研究成果,而且很多工作还在继续。”

  此项发现是由约瑟夫.缲德劳斯克博士和他领导的哈佛大学研究人员首先公布的。约瑟夫现在波士顿达纳法伯癌症研究所工作。报告结果发表在2月27日《自然》杂志上。

  艾滋病毒的发病原理是病毒先进入细胞内部,强占细胞组织,并用来不断进行自我复制。但是猴子体内有一种名为TRIM5-alpha的蛋白成分,可以阻止艾滋病毒进入健康细胞后脱落自身保护层。虽然对于病毒保护层的脱落问题还有待进一步认识,但是科学家认为这是艾滋病毒感染周期的一个重要环节。

  加利福尼亚大学一位研究艾滋病的微生物专家称,人类体内也有名为TRIM5-alpha的成分,但是抵抗艾滋病毒的能力远远不如猴子体内的同类成分。

  哥伦比亚大学一位生物化学家称,“由于这个报告的出台,各个大学的实验室都将就此问题进行研究。”

  缲德劳斯克博士称在动物身上还可能找到治疗其它病毒的成分。“我们发现的也许只是自然预防系统中的第一个例子,通过同样的方法,我们很可能找到对抗其它病毒的成分。”

  艾滋病毒是一种逆转录酶病毒,它可以把基因信息写入感染细胞当中,并且进行不断的复制。所以一旦感染,就很难根除。但是逆转录酶病毒也有弱点,它们如果一开始找不到立足点的话,就会很快消亡。所以TRIM5-alpha蛋白有助于在感染的初始阶段阻止病毒的蔓延。“我们知道艾滋病毒也可以感染猴子的细胞,但是感染一开始就被控制住或者终止了。只是我们还不清楚具体的控制时间。”
我打算做大鼠组织的DAPK1--死亡蛋白相关激酶的WB,但是找到的抗体都只是抗人或猴的,但是国外文献上有人拿这种抗人或猴的抗体做大鼠也做的出,我不知道是否可靠,特请各位大侠指教?万分感谢!
请教各位大神,猴细胞的抗体是不是可以用抗人的?比如我养的是猴小梁网细胞,一抗用兔抗人,二抗用羊抗兔可不可以?因为基本上所有抗体的种属反应性都没有标明猴的,是不是只要标明与人有反应性就可以适用于猴子细胞?
现在要做的实验要用猴子的细胞,但是问很多家都说物种少见,没有我要的抗体。。。。。。我看很多文献也用的我这种细胞啊,虽然没有用和我完全一样的抗体的。。。这可怎么办呢?
在网上看到一篇文章,ELISA检测猴血清中的抗体二抗用的是酶标羊抗人IgG或羊抗猴IgG,结果竟然是酶标羊抗人IgG的阳性读值更好,为什么呢?这是可能的吗?
即使与人猴IgG同源性有98%,似乎也解释不通啊!
请多多指教!
实验需要猪、猫、猴平滑肌抗体,苦于不知哪家公司有销,这三个种属的竟找不到任一种属,敬请指点!
有交叉反应也行啊。
谢谢!!!