产品名称:牛肿瘤坏死因子α(TNF-α)ELISA Kit
仪器介绍
◆采用一只盖革-弥勒计数管来测定α、β、γ和X射线辐射 ◆“安全第一”(Safety First)的校准功能能够避免校准人员的辐射接触 ◆检测仪符合欧洲CE认证要求
主要特点
◆内置卤素淬灭剂GM探测器,对α、β射线源的灵敏度很高 ◆四位液晶显示,可选择mR/hr、CPM、mSv/hr、CPS或Total/Timer等单位 ◆总计数/定时器功能对轻微污染进行定时的精确检测,定时时间可选择1分钟-- 24小时
技术参数
◆测量范围:mR/hr(毫伦/小时):0.001—110.0,CPM(每分钟计数):0—300,000 μSv/hr(微希伏/小时):0.01—1,100,CPS(每秒钟计数):0—5,000,总计数: 1—9,999,000 ◆效 率:Sr-90(546kev,2.3MeV βmax)约75% C-14(156kev βmax)约11% Bi-210(1.2MeV βmax)约64% Am-241(5.5MeV α)约36% ◆灵 敏 度:3500CPM/ mR/hr(对于Cs-137) ◆精 度:±15% ◆温度范围:-10℃---+50℃ ◆电 源:1节9V碱性电池,电池寿命 200小时◆尺寸重量:150×80×30mm 350克(含电池)
应用领域
◆探测和测定表面沾污◆在操作放射性核素时监测可能存在的放射性暴露量◆调查环境污染◆测定惰性气体及其它低能放射性核素◆建筑装饰材料放射测定 射线危害:低剂量的放射性射线辐射(天然背景辐射的变化范围),对人体无害或风险甚低,但达到一定剂量则会对人体有害,可引起癌症、白内障、不孕症、突变、萎缩效应、寿命减短,甚至死亡
应用:
侦测放射性射线,以采取相应防护措施。海关和边境巡逻,政府执法部门,检疫检验,应急事故处理,核电厂、银行、政府、实验室等部门安全巡查,医学废料处理,消防队,采矿业,科学实验,个人保护,连续监测
参考信息(来自中国辐射防护研究院)
居民的剂量限值为每年1mSv。即0.114μSv/hr。
放射性职业人员剂量限值为每年20mSv,但任何一年不能超过50mSv。
1Felis Interferon α(IFN-α)ELISA KitCatalog No. CSB-E04547Fe(96 T) This immunoassay kit allows for the in vitro quantitative determination of felisIFN-α concentrations in serum, plasma and Tissue Homogenates. Expiration date six months from the date of manufacture FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES.2PRINCIPLE OF THE ASSAYThe microtiter plate provided in this kit has been pre-coated withan antibody specific to IFN-α. Standards or samples are thenadded to the appropriate microtiter plate wells with abiotin-conjugated antibody preparation specific for IFN-α andAvidin conjugated to Horseradish Peroxidase (HRP) is added toeach microplate well and incubated. Then a TMB (3,3',5,5'tetramethyl-benzidine) substrate solution is added to each well.Only those wells that contain IFN-α, biotin-conjugated antibodyand enzyme-conjugated Avidin will exhibit a change in color. Theenzyme-substrate reaction is terminated by the addition of asulphuric acid solution and the color change is measuredspectrophotometrically at a wavelength of 450 nm ± 2 nm. Theconcentration of IFN-α in the samples is then determined bycomparing the O.D. of the samples to the standard curve.DETECTION RANGE15.6 pg/ml-1000 pg/ml. The standard curve concentrations usedfor the ELISA’s were 1000 pg/ml, 500 pg/ml, 250 pg/ml, 125pg/ml, 62.5 pg/ml, 31.2 pg/ml, 15.6 pg/ml.3SPECIFICITYThis assay recognizes felis IFN-α. No significant cross-reactivityor interference was observed.SENSITIVITYThe minimum detectable dose of felis IFN-α is typically less than3.9 pg/ml.The sensitivity of this assay, or Lower Limit of Detection (LLD)was defined as the lowest protein concentration that could bedifferentiated from zero.MATERIALS PROVIDEDReagent QuantityAssay plate 1Standard 2Sample Diluent 1 x 20 mlBiotin-antibody Diluent 1 x 10 mlHRP-avidin Diluent 1 x 10 mlBiotin-antibody 1 x 120μlHRP-avidin 1 x 120μlWash Buffer1 x 20 ml(25×concentrate)TMB Substrate 1 x 10 mlStop Solution 1 x 10 ml4STORAGE1. Unopened test kits should be stored at 2-8C upon receiptand the microtiter plate should be kept in a sealed bag. Thetest kit may be used throughout the expiration date of the kit,provided it is stored as prescribed above. Refer to thepackage label for the expiration date.2. Opened test plate should be stored at 2-8C in the aluminumfoil bag with desiccants to minimize exposure to damp air. Thekits will remain stable until the expiring date shown, provided itis stored as prescribed above.3. A microtiter plate reader with a bandwidth of 10 nm or lessand an optical density range of 0-3 OD or greater at 450nmwavelength is acceptable for use in absorbancemeasurement.REAGENT PREPARATIONBring all reagents to room temperature before use.1. Wash Buffer If crystals have formed in the concentrate,warm up to room temperature and mix gently until thecrystals have completely dissolved. Dilute 20 ml of WashBuffer Concentrate into deionized or distilled water to prepare500 ml of Wash Buffer.52. Standard Centrifuge the standard vial at 6000-10000rpmfor 30s. Reconstitute the Standard with 1.0 ml of SampleDiluent. This reconstitution produces a stock solution of 1000pg/ml. Allow the standard to sit for a minimum of 15 minuteswith gentle agitation prior to making serial dilutions. Theundiluted standard serves as the high standard (1000 pg/ml).The Sample Diluent serves as the zero standard (0 pg/ml).Prepare fresh for each assay. Use within 4 hours and discardafter use.3. Biotin-antibody Centrifuge the vial before opening. Diluteto the working concentration using Biotin-antibodyDiluent(1:100), respectively.4. HRP-avidin Centrifuge the vial before opening. Dilute to theworking concentration using HRP-avidin Diluent(1:100),respectively.Precaution: The Stop Solution provided with this kit is an acid solution. Weareye, hand, face, and clothing protection when using this material.OTHER SUPPLIES REQUIRED Microplate reader capable of measuring absorbance at 450nm, with the correction wavelength set at 540 nm or 570 nm. Pipettes and pipette tips.6 Deionized or distilled water. Squirt bottle, manifold dispenser, or automated microplatewasher. An incubator which can provide stable incubation conditionsup to 37°C±0.5°C.SAMPLE COLLECTION AND STORAGE Serum Use a serum separator tube (SST) and allowsamples to clot for 30 minutes before centrifugation for 15minutes at 1000 g. Remove serum and assay immediately oraliquot and store samples at -20°C. Centrifuge the sampleagain after thawing before the assay. Avoid repeatedfreeze-thaw cycles. Plasma Collect plasma using citrate, EDTA, or heparin asan anticoagulant. Centrifuge for 15 minutes at 1000 g within30 minutes of collection. Assay immediately or aliquot andstore samples at -20°C. Centrifuge the sample again afterthawing before the assay. Avoid repeated freeze-thaw cycles. Tissue Homogenates 100mg tissue was rinsed with1X PBS, homogenized in 1 mL of 1X PBS and storedovernight at -20° C. After two freeze-thaw cycles wereperformed to break the cell membranes, the7homogenates were centrifuged for 5 minutes at 5000 x g,2 - 8°C. The supernate was assayed and removedimmediately. Alternatively, aliquot and store samples at-20°C or -80℃. Centrifuge the sample again afterthawing before the assay. Avoid repeated freeze-thawcycles.Note: Grossly hemolyzed samples are not suitable for use in this assay.ASSAY PROCEDUREBring all reagents and samples to room temperature before use. It isrecommended that all samples, standards, and controls be assayed in duplicate.All the reagents should be added directly to the liquid level in the well. Thepipette should avoid contacting the inner wall of the well.1. Add 100μl of Standard, Blank, or Sample per well. Cover withthe adhesive strip. Incubate for 2 hours at 37°C.2. Remove the liquid of each well, don’t wash.3. Add 100μl of Biotin-antibody working solution to each well.Incubate for 1 hour at 37°C. Biotin-antibody workingsolution may appear cloudy. Warm up to room temperatureand mix gently until solution appears uniform.4. Aspirate each well and wash, repeating the process threetimes for a total of three washes. Wash: Fill each well withWash Buffer (200μl) and let it stand for 2 minutes, then8remove the liquid by flicking the plate over a sink. Theremaining drops are removed by patting the plate on a papertowel. Complete removal of liquid at each step is essential togood performance.5. Add 100μl of HRP-avidin working solution to each well.Cover the microtiter plate with a new adhesive strip. Incubatefor 1 hour at 37°C.6. Repeat the aspiration and wash five times as step 4.7. Add 90μl of TMB Substrate to each well. Incubate for 10-30minutes at 37°C. Keeping the plate away from drafts andother temperature fluctuations in the dark.8. Add 50μl of Stop Solution to each well when the first fourwells containing the highest concentration of standardsdevelop obvious blue color. If color change does not appearuniform, gently tap the plate to ensure thorough mixing.9. Determine the optical density of each well within 30 minutes,using a microplate reader set to 450 nm.CALCULATION OF RESULTSUsing the professional soft "Curve Exert 1.3" to make a standard curve isrecommended, which can be downloaded from our web.Average the duplicate readings for each standard, control, andsample and subtract the average zero standard optical density.9Create a standard curve by reducing the data using computersoftware capable of generating a four parameter logistic (4-PL)curve-fit. As an alternative, construct a standard curve by plottingthe mean absorbance for each standard on the x-axis againstthe concentration on the y-axis and draw a best fit curve throughthe points on the graph. The data may be linearized by plottingthe log of the IFN-α concentrations versus the log of the O.D.and the best fit line can be determined by regression analysis.This procedure will produce an adequate but less precise fit ofthe data. If samples have been diluted, the concentration readfrom the standard curve must be multiplied by the dilution factor.LIMITATIONS OF THE PROCEDURE The kit should not be used beyond the expiration date on thekit label. Do not mix or substitute reagents with those from other lots orsources. It is important that the Standard Diluent selected for thestandard curve be consistent with the samples beingassayed. If samples generate values higher than the highest standard,dilute the samples with the appropriate Standard Diluent andrepeat the assay.10 Any variation in Standard Diluent, operator, pipettingtechnique, washing technique, incubation time ortemperature, and kit age can cause variation in binding. This assay is designed to eliminate interference by solublereceptors, binding proteins, and other factors present inbiological samples. Until all factors have been tested in theImmunoassay, the possibility of interference cannot beexcluded.TECHNICAL HINTS Centrifuge vials before opening to collect contents. When mixing or reconstituting protein solutions, always avoidfoaming. To avoid cross-contamination, change pipette tips betweenadditions of each standard level, between sample additions,and between reagent additions. Also, use separate reservoirsfor each reagent. When using an automated plate washer, adding a 30 secondsoak period following the addition of wash buffer, and/orrotating the plate 180 degrees between wash steps mayimprove assay precision.11 To ensure accurate results, proper adhesion of plate sealersduring incubation steps is necessary. Substrate Solution should remain colorless or light blue untiladded to the plate. Keep Substrate Solution protected fromlight. Substrate Solution should change from colorless or lightblue to gradations of blue. Stop Solution should be added to the plate in the same orderas the Substrate Solution. The color developed in the wellswill turn from blue to yellow upon addition of the Stop Solution.Wells that are green in color indicate that the Stop Solutionhas not mixed thoroughly with the Substrate Solution.
小鼠血浆α颗粒膜蛋白进口原装,Mouse GMP-140 ELISA Kit检测报价加样:.标本为血清:最好将血液先自然存放1-2小时后,再用3000rmp离心15分钟;标本为血浆:必须使用含抗凝剂的血液标本收集管,采血后必须立即颠倒采血管混合5-10次,放置一段时间后,3000rpm离心15分钟;若在几天内检测,可放在2-8℃冰箱中,若要贮存,则置于-20℃的低温冰箱内。 2.加样后及时放入孵箱。 3.加酶试剂后用吸水纸在酶标板表面轻拭吸干。 4.如果采用AT或其他全自动加样,最好选择FAME或其他后处理仪器加酶试剂。 5.标本较多时,请分批操作。
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小鼠血浆α颗粒膜蛋白进口原装,Mouse GMP-140 ELISA Kit检测报价
DH5α感受态细胞 目录号:1802
v 产品组成、储存、稳定性:
储存:-70 ℃ 保存,避免反复冻融 v 产品介绍: 本公司生产的DH5а感受态细胞是采用大肠杆菌DH5а菌株经特殊工艺处理得到的感受态细胞,可用于DNA 的化学转化。使用pUC19 质粒检测,转化效率可达108 ,-70 ℃ 保存几个月转化效率不发生改变。 每支感受态可以酌情分装使用,降低了实验的成本。质量稳定,使用方便,质优价廉。 DH5а 菌株的基因型为:F -φ80 lacZΔM15Δ(lacZYA-argF)U169 end A1 recA1 hsdR17(rk -,mk -) sup E44 λ- thi-1 gyrA96 relA1 phoA v 产品特点: 一种用于铺制与培养质粒平板和粘粒平板的重级缺陷的抑制型株。其φ80 lacZΔM15 基因的产物可与pUC 载体编码的β-半乳糖苷酶氨基端实现α互补,可用于蓝白斑筛选。 |
本试剂盒只能用于科学研究,不得用于医学诊断,具体说明书请联系客服索取,本说明书是通用模板,有些数据不准确.产品规格48T/96T 国产/RD进口分装/TSZ进口原装工作原理试剂盒采用双抗体一步夹心法酶联免疫吸附试验(ELISA)。往预先包被样本抗体的包被微孔中,依次加入标本、标准品、HRP标记的检测抗体,经过温育并彻底洗涤。用底物TMB显色,TMB在过氧化物酶的催化下转化成蓝色,并在酸的作用下转化成最终的黄色。颜色的深浅和样品中的样本呈正相关。用酶标仪在450nm 波长下测定吸光度(OD 值),计算样品浓度。
注意事项1. 试剂盒保存在2-8℃,使用前室温平衡20分钟。从冰箱取出的浓缩洗涤液会有结晶,这属于正常现象,水浴加热使结晶完全溶解后再使用。2. 实验中不用的板条应立即放回自封袋中,密封(低温干燥)保存。3. 浓度为0的S0号标准品即可视为阴性对照或者空白;按照说明书操作时样本已经稀释5倍,最终结果乘以5才是样本实际浓度。4. 严格按照说明书中标明的时间、加液量及顺序进行温育操作。5. 所有液体组分使用前充分摇匀。
性能特点1. 准确性:标准品线性回归与预期浓度相关系数R值,大于等于0.9900。2. 灵敏度:最低检测浓度小于(参考说明书)3. 特异性:不与其它可溶性结构类似物交叉反应。4. 重复性:板内、板间变异系数均小于15%。5. 贮藏:2-8℃,避光防潮保存。6. 有效期:6个月
免责声明1. 试剂盒仅供研究使用,不得用于临床实验或人体实验,否则所产生的一切后果,由实验者承担,本公司概不负责。 严格按照说明书操作,实验者违反说明书操作,后果由实验者承担。本品为科研试剂,只对单位实验室学校等正规用途出售。如需资料请向客服索取!企业网站:www.yuduobio.com数十万产品随亲挑选,正规生物公司,可开具正规机打发票。发票需加6个点。
公司介绍
上海羽朵生物科技有限公司生产销售elisa试剂盒、动物血清、血浆、全血、抗原抗体、金标试剂盒检测卡、抗血清、生物试剂、培养基、实验室仪器耗材、化学试剂、生物制品、标准品、对照品、生化免疫制品、免疫亲和柱、菌株、质粒、室内质控品、细胞、冰袋、代理进口产品等量大从优!牛血清白蛋白(BSA)1kg 3000元,纯度为>99%可定做各种浓度的绵羊红细胞,兔血红细胞,鸡血红细胞。出售补体实验所需的溶血素,试剂盒,蛇毒因子,黄曲霉毒素B1标准品,以色列进口原装,纯度99.8%,1-100mg规格齐全,随货带防伪证书,送检测试纸。黄曲霉毒素B1标准品,新加坡进口,纯度>99%,1-100mg规格齐全,随货带防伪证书,送检测试纸。另出售环氧化苯并芘标准品,纯度99.9%,100mg,500mg,1g三种规格现货促销。。。动物血清系列:标准胎牛血清、特级胎牛血清、标准新生牛血清、特级新生牛血清、优级新生牛血清、标准马血清、特级马血清、山羊血清、绵羊血清、兔血清、鸡血清、大牛血清、小牛血清、猪血清、狗血清、驴血清、豚鼠血清、大鼠血清、小鼠血清、巴比西鼠血清各种动物全血:抗凝全血.脱纤维全血.脱纤维裂解裂解血.抗凝裂解血.各种动物血浆:(胎牛血清、新生牛血浆、大牛血浆、小牛血浆、绵羊血浆、山羊血浆、猪血浆、驴血浆、马血浆、、狗血浆、兔血浆、大鼠血浆、小鼠血浆、豚鼠血浆)
出售各种真菌毒素类标准品:3-4’苯并芘,环氧化苯并芘、黄曲霉毒素B1,B2,G1,G2,M1,M2、脱氧雪腐镰刀菌烯酮(DON呕吐毒素)、3-乙酰基脱氧雪腐镰刀菌烯醇(3-A-DON)、15-乙酰基脱氧雪腐镰刀菌烯醇(15-A-DON)、雪腐镰刀菌烯醇(NIV)、伏马毒素B1B2、赭曲霉毒素A、玉米赤霉烯酮、T2毒素、HT2毒素、桔青霉素/桔霉素、棒曲霉素/展青霉素、杂色曲霉素、黄曲霉毒素混标液体 (SIGMA)、黄曲霉毒素混标液体 (FERMENTEK)、黄曲霉毒素M1液体标品(10ug/ml)、黄曲霉毒素M1液体标品(0.5ug/ml)、赭曲霉毒素A液体标品、 黄曲霉毒素B1液体标品
实验室常用试剂(免疫组化/分子试剂盒,生物缓冲液/染色液,核酸/蛋白质Marker,分离试剂)生物制品(核酸及其衍生物,氨基酸/蛋白质,酶/辅酶,维生素/抗生素/激素)等欢迎经销商代理商洽谈合作事宜!本公司诚信经营,如有质量问题可免费退换,请大家放心使用,仅供科研实验使用,欢迎大家选购!谢谢!如需其他产品请联系客服索要报价。相关产品推荐:人PL7抗体/抗苏氨酰tRNA合成酶(PL7)ELISA试剂盒 人PL12抗体/抗丙氨酰tRNA合成酶(PL12/AlaRS)ELISA试剂盒 人抗Mi2抗体(anti-Mi2-Ab)ELISA试剂盒 人抗Ku抗体(anti-Ku-Ab)ELISA试剂盒 人抗IgA抗体(anti-IgA-Ab)ELISA试剂盒 人抗神经元核抗体1型/抗Hu抗体(ANNA-1/Hu)ELISA试剂盒 人抗DNA酶B抗体(anti-DNase B)ELISA试剂盒 人抗BP180抗体(BP180-Ab)ELISA试剂盒 人抗BB抗体(BB-Ab)ELISA试剂盒 人抗平滑肌抗体(ASMA)ELISA试剂盒人抗肝细胞膜抗体(LMA)ELISA试剂盒人抗肝特异性脂蛋白抗体(LSP)ELISA试剂盒人抗眼肌抗体(EMAb)ELISA试剂盒人抗补体1q抗体(C1q)ELISA试剂盒 人抗内因子抗体(IFA)ELISA试剂盒人抗磷脂抗体(Apl/APA)ELISA试剂盒人抗组蛋白抗体(AHA)ELISA试剂盒人晶体蛋白α(Cryα)ELISA试剂盒人晶体蛋白β(Cryβ)ELISA试剂盒 人抗胶原蛋白抗体(CLA)ELISA试剂盒人抗环胍氨酸肽抗体(CCP)ELISA试剂盒人抗核周因子抗体(APF)ELISA试剂盒
运蛋白抗体M57513 0.2ml
Anti-Mfn1 线粒体融合蛋白1抗体M57514 0.1ml
Anti-MGMT O6甲基鸟嘌呤DNA甲基转移酶抗体M57515 0.1ml
anti-MT 金属基质硫蛋白抗体M57516 0.1ml
anti-MGr1-Ag/37LRP 层粘连蛋白受体1抗体M575170.2
Anti-MICA 一种细胞应激分子抗体M57518 0.1ml
Anti-Midnolin isoform Protein 1 中脑核仁蛋白1抗体M57519 0.1ml
Anti-Midnolin isoform Protein 2 中脑核仁蛋白2抗体M57520 0.2ml
Anti-MIF 巨噬细胞移动抑制因子抗体M57521 0.1ml
Anti-MIP-1α 巨噬细胞炎症因子1α抗体M57522 0.1ml
Anti-MIP-1β 巨噬细胞炎症因子1β 抗体M57523 0.2ml
Anti-MMP-1 基质金属蛋白酶-1抗体M57524 0.1ml
Anti-MMP-13 基质金属蛋白酶13抗体M57525 0.1ml
Anti-MMP-14 基质金属蛋白酶-14抗体M57526 0.1ml
小鼠转化生长因子α(TGF-α)elisa酶联免疫检测试剂盒使用说明书Anti-MMP-2 基质金属蛋白酶-2抗体M57527 0.1ml
Anti-MMP-3 基质金属蛋白酶-3抗体M57528 0.1ml
Anti-MMP-7 基质金属蛋白酶-7抗体M57529 0.1ml
Anti-MMP-9 基质金属蛋白酶-9抗体M57530 0.1ml
Anti-β-2-MG 鼠抗人β2微球蛋白抗体M57531 0.1ml
Anti-Mo anti-KLH 小鼠抗血蓝蛋白抗体M57532 0.2ml
Anti-MOG 髓鞘少树突胶质细胞糖蛋白抗体M57533 0.2ml
Anti-Mouse anti-human HAS 鼠抗人血清白蛋白单克隆抗体M57534 0.1ml
Anti-Mouse IgA 兔抗小鼠IgA抗体M57535 0.2ml
Anti-MPO 髓过氧化物酶抗体M57536 0.1ml
Anti-MRP1 多药耐药相关蛋白1抗体M57537 0.1ml
Anti-MRP2 多药耐药相关蛋白2抗体M57538 0.1ml
Anti-MRP3 多药耐药相关蛋白3抗体M57539 0.1ml
Anti-MrpL28 线粒体核糖体蛋白L28抗体M57540 1ml
Anti-MSH-2 错配修复蛋白2抗体M57541 0.1ml
anti-MLH1 错配修复蛋白1抗体M57542
免费代测 大鼠肿瘤坏死因子α(TNF-α)elisa试剂盒 Y11721A
Y11715A | 大鼠血管内皮细胞粘附分子1(VCAM-1/CD106)Elisa试剂盒 |
Y11716A | 大鼠白介素8(IL-8/CXCL8)Elisa试剂盒 |
Y11717A | 大鼠可溶性核因子κB受体活化因子配基(sRANKL)Elisa试剂盒 |
Y11718A | 大鼠β干扰素(IFN-β/IFNB)Elisa试剂盒 |
Y11719A | 大鼠血小板因子3(PF-3)Elisa试剂盒 |
Y11720A | 大鼠血管内皮细胞生长因子(VEGF)Elisa试剂盒 |
Y11721A | 大鼠肿瘤坏死因子α(TNF-α)Elisa试剂盒 |
免费代测 大鼠肿瘤坏死因子α(TNF-α)Elisa试剂盒 Y11721A
Y11715A | 大鼠血管内皮细胞粘附分子1(VCAM-1/CD106)Elisa试剂盒 |
Y11716A | 大鼠白介素8(IL-8/CXCL8)Elisa试剂盒 |
Y11717A | 大鼠可溶性核因子κB受体活化因子配基(sRANKL)Elisa试剂盒 |
Y11718A | 大鼠β干扰素(IFN-β/IFNB)Elisa试剂盒 |
Y11719A | 大鼠血小板因子3(PF-3)Elisa试剂盒 |
Y11720A | 大鼠血管内皮细胞生长因子(VEGF)Elisa试剂盒 |
Y11721A | 大鼠肿瘤坏死因子α(TNF-α)Elisa试剂盒 |
免费代测 大鼠肿瘤坏死因子α(TNF-α)Elisa试剂盒 Y11721A
上海卒瑞生物科技有限公司是国内专业研发生产Elisa试剂盒、金标检测试剂盒、酶联法检测试剂盒的供应商,且供销各类生化试剂(进口国产)、培养基、动物血清、抗原、抗体、实验试剂、人及动物Elisa试剂盒、氨基酸类、实验室耗材、实验室仪器、低温恒温槽、雪花制冰机、恒温油槽等各类产品。本公司是专门从事生物科技领域内的技术开发、技术咨询、销售为一体的科学技术服务公司。为国内外科研院所、学校、实验室、制药、化工、环境保护及卫生检疫部门等相应企业提供科研实验技术服务。我们拥有先进的研发技术和雄厚的科学实力,完整、科学的质量管理体系。本公司以诚信、实力和产品质量获得业界的认可,与多家生产商建立了长期稳定的合作关系。欢迎各界朋友莅临参观、指导和业务洽谈。
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