CC-118A透明槽加热型恒温水浴可以方便观察浴槽中的变化。工作温度为100℃,接泵接口可以用于外循环,温度稳定性符合DIN12876标准。 CC-118A透明槽加热型恒温水浴技术指标 内槽体积:18L; 加热功率:2KW; 温度范围:室温~100℃ 开口尺寸(mm):302*325 外形尺寸(mm):333*520*335
订货号:2001.0005.04
技术参数:德国凯驰Karcher(广州博励)全自动洗地机吸干机 | |
洗地宽度 毫米 | 800 |
吸水宽度 毫米 | 990 |
净/污水箱 升 | 120/120 |
洗地效率 平米/小时 | 3200 |
刷子转速 转/分 | 200 |
刷子触地压力(可调) | 36 克/平方厘米 |
电机功率 瓦 | 1660 |
重量 公斤 | 170 |
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。
技术参数 | |||
通道数量 | 96 | 通道间隔 | 50GHz, 100GHz |
通道频率 | 196.45~191.7THz | 最大输入功率 | 500mW; 27dBm |
带宽 | 1526.05~1563.86 nm | 光源接头 | SC/PC Standard |
测量速度 | 4 Sec. (all 96ch.) | 电池 | 锂聚合物电池, 1800毫安时,3.7伏 |
测量范围 | +10~-40dBm | 电池工作时长 | 充满电后单次使用620分钟 |
测量精度 | ± 1.0dB @ -40 dBm | 电流消耗(Max) | 0.25A |
显示屏分辨率 | 0.01dB | 电力消耗 | 0.925W |
显示单位 | dB, dBm,nm,THz | 显示 | 3.5” TFT-LCD, 16bit color, 240*320 |
重量 | 0.6 kg | 尺寸 | 196*95*40 mm |
温度 (环境条件) | -20 to +55 °C (操作环境) | 湿度 (最大无冷凝) | 95% (操作环境) |
-35 to +65°C (储存环境) | 85% (储存环境) |
上海东晟轴承具有一定名气和规模的大型进口轴承供应商轴承型号查询,具备多年开拓国内外机电搜轴网产品专项营销的广泛渠道和较强的经济实力,我公司主要专业供应GAR50-DO-2RS轴承FAG、瑞典SKF进口轴承、美国TIMKEN、德国FAG与INA等五大品牌,同时还供应日本IKO、NTN等四个品牌,现货供应,交期短。欢迎来电咨询GAR50-DO-2RS轴承尺寸、价格、技术支持或同型号其他品牌替换等详细资料!如果您对FAGGAR50-DO-2RS轴承有疑问,请联系我们获取更多GAR50-DO-2RS轴承的最新信息 FAG轴承。FAG供应商服务领域包括:冶金、电力、石化、建筑机械等,IKO轴承并在铁路、钢铁、造纸、水泥、矿山等领域更是一枝独秀。联系方式:电话 : 传真: NADELLA轴承GAR50-DO-2RS轴承 GAR50-DO-2RS轴承价格 GAR50-DO-2RS轴承尺寸GAR50-DO-2RS轴承报价 GAR50-DO-2RS轴承图片NADELLA轴承 【GAR50-DO-2RS轴承】尺寸参数表:轴承型号:GAR50-DO-2RS轴承品牌:FAG轴承系列:杆端轴承NADELLA导轨经销商 上海东晟轴承有限公司提供FAG轴承GAR50-DO-2RS的单梁起重机、包装设备、管道泵、化工设备配件、冷冻机、等技术参数。我公司是瑞典NSK、德国FAG和INA、美国TIMKEN轴承的进口轴承地区的经销商。公司秉承“质优、专业、高效”的经营上海NSK轴承代理商理念,为广大客户提供最优的轴承品质、最合理的搜轴网价格、最满意的服务。推荐型号:SNR7304BDB轴承 7303BDB SNR 7301BDB轴承 SNR 7300BDB SNR7302BDB SNR7240BDB轴承 7244BDB SNL528轴承 FSNL530 SNL530轴承 SNL532 FSNL532轴承 SNL312TURU SNL313TURU轴承 SNL314TURU 7321B/DT 6316-2Z轴承 24028CK30E4 W629轴承 22310RHK+H2310 7022CDB轴承 SKF轴承 德国NADELLA轴承 公司网站:http://www.bearings365.comhttp://www.zcsearch.comhttp://www.sh-bearings.comhttp://www.zhoucheng188.comhttp://www.ikont.com.cnhttp://www.shdszc.com参考资料:http://www.zhoucheng188.com/FAG/GAR50-DO-2RS.html
上海 | 江苏 | 浙江 | 安徽 | 福建 | 江西 | 山东 | 山西| 湖北 | 湖南 | 广东 | 广西 | 海南 | 重庆 | 四川 | 贵州 | 云南
苏州米顿罗GB系列机械隔膜计量泵
GB0080 GB0180 GB0250 GB0350 GB0450 | 82 167 237 334 416 | 1.0 1.0 1.0 1.0 1.0 | 36 72 102 144 180 |
GB0500 GB0600 | 464 583 | 0.7 0.7 | 144 180 |
GB0700 GB1000 GB1200 | 656 946 1200 | 0.35 0.35 0.35 | 102 144 180 |
GB1500 GB1800 | 1500 1800 | 0.3 0.3 | 180 206 |
G系列机械隔膜计量泵 特点 •可变偏心机构调节,脉动平缓 •多种材质及泵头结构可选-PVC、 PVDF、316SS、高粘及浆料泵头 •机械驱动PTFE膜片 •物料侧无隔膜护盘,便于物料通过 •三种自动控制方式,适合各种控制需要 •手动/电动冲程调节可选 •冲程可调0~100%(自动/手动)
•冲程在静态及动态条件下均可调节 •大液体温度40℃*•稳态精度:±2%(10%~100%) •大吸程:3m水柱*•大吸入压力:20m水柱 •可选双隔膜泵头结构 •建议维护周期:≤1.0MPa4000h≤0.7MPa8000h上海 | 江苏 | 浙江 | 安徽 | 福建 | 江西 | 山东 | 山西| 湖北 | 湖南 | 广东 | 广西 | 海南 | 重庆 | 四川 | 贵州 | 云南
自动控制方式选择 •电动冲程控制器 接受外部控制信号,调节计量泵冲程长度, 从而改变计量泵输出流量。 G系列计量泵选择HE型。其中GB系列可选ECC防爆型。 •变频控制器 接受外部控制信号,调节计量泵冲程速度。 供电:380V/50Hz三相/220V/50Hz单相 控制信号:4~20mA•电机开关控制器(VARIPULSE): 反用于GM系列计量泵,用于控制三相电机, 改变冲程频率,从而调节计量泵输出流量。 V型-与计量泵一体式安装,VR型-与计量泵分体式安装
电动冲程控制器技术参数 | ||
类型 | HE | ECC(GB) |
供电 | 220V±10%,50/60Hz | |
控制信号 | 4~20mA | |
防护等 | IP65 | NEMA4 |
反馈信号 | 4~20mA | 4~20mA |
功耗 | 20VA | N/A |
环境温度 | -10℃~+40℃ | -40℃~+50℃ |
输入阻抗 | 120Ω | 250Ω |
输出负载 | 100~500Ω | N/A |
执行时间 | 0~100%/150S | 0~100%/180S |
防爆等 | 无 | 1区、IB、C和D组 |
润滑油
泵型 | 容积 | 环境温度<-5℃ | 环境温度≥-5℃ |
GB | 3L | 美孚600XP68 | 美孚600XP220 |
GM | 0.8L | 美孚600XP68 | 美孚600XP220 |
泵头过流部件材质
泵头材质 | 阀体 | 阀座 | 阀球 | 隔膜 | 密封圈 | 进出口连接 | ||
GM0002~GM0050 | ||||||||
PVC | PVDF | PVDF | 陶瓷 | PTFE | 氟橡胶 | PVC | ||
PVDF | PVDF | PVDF | 陶瓷 | PTFE | PTFE | PVDF | ||
316SS | 316SS | 316SS | 316SS | PTFE | 氟橡胶 | 316SS | ||
GM0090~GM0500 | ||||||||
PVC | PVC | PVC | 玻璃 | PTFE | 氟橡胶 | PVC | ||
PVDF | PVDF | PVDF | 陶瓷 | PTFE | PTFE | PVDF | ||
316SS | 316SS | 316SS | 316SS | PTFE | 氟橡胶 | 316SS | ||
GB0080~GB1500 | ||||||||
PVC | PVC | PVC | 陶瓷 | PTFE | 氟橡胶 | PVC | ||
PVDF | PVDF | PVDF | 陶瓷 | PTFE | PTFE | PVDF | ||
316SS | 316SS | 316SS | 316SS | PTFE | 氟橡胶/PTFE | 316SS | ||
GB1800 | ||||||||
泵头材料 | 阀体/衬套 | 阀板/升程限位板 | 弹簧 | 隔膜 | 密封圈 | 进出口连接 | ||
PVC | PVC | PVC | 哈氏合金C | PTFE | 氟橡胶 | PVC | ||
PVDF | PVDF | PVDF | 哈氏合金C | PTFE | PTFE | PVDF | ||
316SS | 316SS | 316SS | 哈氏合金C | PTFE | 氟橡胶 | 316SS | ||
美国米顿罗GB0600机械隔膜计量泵/GB0600米顿罗加药泵/苏州加药泵
美国米顿罗GB0700机械隔膜计量泵/GB0700米顿罗加药泵/苏州加药泵
米顿罗GB1000机械隔膜计量泵/GB1000米顿罗加药泵/苏州加药泵
美国米顿罗GB1200机械隔膜计量泵/GB1200米顿罗加药泵/苏州加药泵
GB1500机械隔膜计量泵/美国米顿罗GB1500加药泵/苏州加药泵
GB1800机械隔膜计量泵/美国米顿罗GB1800加药泵/苏州加药泵
G系列电机驱动机械隔膜计量泵
主要性能参数
流量可达1200升/小时,压力可达1.2MPa
无论泵是否运行,均可在0-100%范围内调节流量
在10%至100%范围内,稳态精度为±2%
允许物料高温度40℃
吸入提升高度可达4米水柱,允许入口压力0.2MPa主要特性
机械驱动隔膜,物料侧无隔膜护盘,便于物料通过
可变偏心机构驱动,确保脉动平缓
铸铝壳体、整体重量轻
耐磨球轴承,工作更稳定
油浴润滑,驱动部件工作寿命更长
PVC、PP、PVDF、316SS、高粘度、浆料等多种材质泵头
双隔膜泵头、多泵并联等可选结构,适合各种过程
三种不同控制方式,适合各种控制系统要求控制方式
电动冲程控制器:可接受外部控制信号,调节冲程长度 供电电源:220V-50Hz-单相 输入信号:4-20mA模拟信号 输出信号:1-5V/4-20mA模拟信号,供记录显示和控制系统使用
变频控制器:可接受外部控制信号,调节冲程速度 供电电源:220V-50Hz-单相/380V-50Hz-3相 输入信号:4-20mA模拟信号
马达控制器:以"开/停"方式控制三相电机,调节输出流量 供电电源:200-240V/50/60Hz/单相 控制方式:可接受4-20mA模拟信号、外部脉冲信号或手动调节GM/GB系列机械隔膜计量泵型号流量压力代码:P代码:S代码:T代码:V代码:K代码:M系列(L/h)(Mpa)PVC316SSPVDF高粘度泵头浆料泵头混合物泵头GB0080821518870081018882598986.8注意:GM0005-GM0240配0.25KW电机,可用于变频、不放大
基本型号包括
GB0180,GB0250,GB0350,GB0450,GB0500,GB0600,GB0700,GB1000,GB1200标准配置:0.75KW电机GB150015000.3GB180018000.3
以上是米顿罗计量泵GM/GB的详细信息,如果您对米顿罗计量泵GM/GB的价格、厂家、型号、图片有什么疑问,请联系我们获取米顿罗计量泵GM/GB的新信息
Rat Interleukin 10(IL-10)
ELISA Kit
Catalog No. CSB-E04595r
(96T)
l This immunoassay kit allows for the in vitro quantitative determination of rat IL-10 concentrations in serum, plasma and Tissue Homogenates.
l Expiration date six months from the date of manufacture
l FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES.
PRINCIPLE OF THE ASSAY
The microtiter plate provided in this kit has been pre-coated with an antibody specific to IL-10. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for IL-10 and Avidin conjugated to Horseradish Peroxidase (HRP) is added to each 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 IL-10, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of IL-10 in the samples is then determined by comparing the O.D. of the samples to the standard curve.
DETECTION RANGE
3.12 pg/ml-200 pg/ml. The standard curve concentrations used for the ELISA’s were 200 pg/ml, 100 pg/ml, 50 pg/ml, 25 pg/ml, 12.5 pg/ml, 6.25 pg/ml, 3.12 pg/ml.
SPECIFICITY
This assay recognizes rat IL-10. No significant cross-reactivity or interference was observed.
SENSITIVITY
The minimum detectable dose of rat IL-10 is typically less than 0.78 pg/ml.
The sensitivity of this assay, or Lower Limit of Detection (LLD) was defined as the lowest protein concentration that could be differentiated from zero.
MATERIALS PROVIDED
Reagent | Quantity |
Assay plate | 1 |
Standard | 2 |
Sample Diluent | 1 x 20 ml |
Biotin-antibody Diluent | 1 x 10 ml |
HRP-avidin Diluent | 1 x 10 ml |
Biotin-antibody | 1 x 120μl |
HRP-avidin | 1 x 120μl |
Wash Buffer | 1 x 20 ml (25×concentrate) |
TMB Substrate | 1 x 10 ml |
Stop Solution | 1 x 10 ml |
STORAGE
1. Unopened test kits should be stored at 2-8°C upon receipt and the microtiter plate should be kept in a sealed bag. The test kit may be used throughout the expiration date of the kit, provided it is stored as prescribed above. Refer to the package label for the expiration date.
2. Opened test plate should be stored at 2-8°C in the aluminum foil bag with desiccants to minimize exposure to damp air. The kits will remain stable until the expiring date shown, provided it is stored as prescribed above.
3. A microtiter plate reader with a bandwidth of 10 nm or less and an optical density range of 0-3 OD or greater at 450nm wavelength is acceptable for use in absorbance measurement.
REAGENT PREPARATION
Bring 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 the crystals have completely dissolved. Dilute 20 ml of Wash Buffer Concentrate into deionized or distilled water to prepare 500 ml of Wash Buffer.
2. Standard Centrifuge the standard vial at 6000-10000rpm for 30s. Reconstitute the Standard with 1.0 ml of Sample Diluent. This reconstitution produces a stock solution of 200 pg/ml. Allow the standard to sit for a minimum of 15 minutes with gentle agitation prior to making serial dilutions. The undiluted standard serves as the high standard (200 pg/ml). The Sample Diluent serves as the zero standard (0 pg/ml). Prepare fresh for each assay. Use within 4 hours and discard after use.
3. Biotin-antibody Centrifuge the vial before opening. Dilute to the working concentration using Biotin-antibody Diluent(1:100), respectively.
4. HRP-avidin Centrifuge the vial before opening. Dilute to the working concentration using HRP-avidin Diluent(1:100), respectively.
Precaution: The Stop Solution provided with this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.
OTHER SUPPLIES REQUIRED
Microplate reader capable of measuring absorbance at 450 nm, with the correction wavelength set at 540 nm or 570 nm.
Pipettes and pipette tips.
Deionized or distilled water.
Squirt bottle, manifold dispenser, or automated microplate washer.
An incubator which can provide stable incubation conditions up to 37°C±0.5°C.
SAMPLE COLLECTION AND STORAGE
l Serum Use a serum separator tube (SST) and allow samples to clot for 30 minutes before centrifugation for 15 minutes at 1000 g. Remove serum and assay immediately or aliquot and store samples at -20°C. Centrifuge the sample again after thawing before the assay. Avoid repeated freeze-thaw cycles.
l Plasma Collect plasma using citrate, EDTA, or heparin as an anticoagulant. Centrifuge for 15 minutes at 1000 g within 30 minutes of collection. Assay immediately or aliquot and store samples at -20°C. Centrifuge the sample again after thawing before the assay. Avoid repeated freeze-thaw cycles.
l Tissue Homogenates 100mg tissue was rinsed with 1X PBS, homogenized in 1 mL of 1X PBS and stored overnight at -20° C. After two freeze-thaw cycles were performed to break the cell membranes, the homogenates were centrifuged for 5 minutes at 5000 x g, 2 - 8°C. The supernate was assayed and removed immediately. Alternatively, aliquot and store samples at -20°C or -80℃. Centrifuge the sample again after thawing before the assay. Avoid repeated freeze-thaw cycles.
Note: Grossly hemolyzed samples are not suitable for use in this assay.
ASSAY PROCEDURE
Bring all reagents and samples to room temperature before use. It is recommended that all samples, standards, and controls be assayed in duplicate. All the reagents should be added directly to the liquid level in the well. The pipette should avoid contacting the inner wall of the well.
1. Add 100μl of Standard, Blank, or Sample per well. Cover with the 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 working solution may appear cloudy. Warm up to room temperature and mix gently until solution appears uniform.
4. Aspirate each well and wash, repeating the process three times for a total of three washes. Wash: Fill each well with Wash Buffer (200μl) and let it stand for 2 minutes, then remove the liquid by flicking the plate over a sink. The remaining drops are removed by patting the plate on a paper towel. Complete removal of liquid at each step is essential to good performance.
5. Add 100μl of HRP-avidin working solution to each well. Cover the microtiter plate with a new adhesive strip. Incubate for 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 10-30 minutes at 37°C. Keeping the plate away from drafts and other temperature fluctuations in the dark.
8. Add 50μl of Stop Solution to each well when the first four wells containing the highest concentration of standards develop obvious blue color. If color change does not appear uniform, 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 RESULTS
Using the professional soft "Curve Exert 1.3" to make a standard curve is recommended, which can be downloaded from our web.
Average the duplicate readings for each standard, control, and sample and subtract the average zero standard optical density. Create a standard curve by reducing the data using computer software capable of generating a four parameter logistic (4-PL) curve-fit. As an alternative, construct a standard curve by plotting the mean absorbance for each standard on the x-axis against the concentration on the y-axis and draw a best fit curve through the points on the graph. The data may be linearized by plotting the log of the IL-10 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 of the data. If samples have been diluted, the concentration read from 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 the kit label.
Do not mix or substitute reagents with those from other lots or sources.
It is important that the Standard Diluent selected for the standard curve be consistent with the samples being assayed.
If samples generate values higher than the highest standard, dilute the samples with the appropriate Standard Diluent and repeat the assay.
Any variation in Standard Diluent, operator, pipetting technique, washing technique, incubation time or temperature, and kit age can cause variation in binding.
This assay is designed to eliminate interference by soluble receptors, binding proteins, and other factors present in biological samples. Until all factors have been tested in the Immunoassay, the possibility of interference cannot be excluded.
TECHNICAL HINTS
Centrifuge vials before opening to collect contents.
When mixing or reconstituting protein solutions, always avoid foaming.
To avoid cross-contamination, change pipette tips between additions of each standard level, between sample additions, and between reagent additions. Also, use separate reservoirs for each reagent.
When using an automated plate washer, adding a 30 second soak period following the addition of wash buffer, and/or rotating the plate 180 degrees between wash steps may improve assay precision.
To ensure accurate results, proper adhesion of plate sealers during incubation steps is necessary.
Substrate Solution should remain colorless or light blue until added to the plate. Keep Substrate Solution protected from light. Substrate Solution should change from colorless or light blue to gradations of blue.
Stop Solution should be added to the plate in the same order as the Substrate Solution. The color developed in the wells will turn from blue to yellow upon addition of the Stop Solution. Wells that are green in color indicate that the Stop Solution has not mixed thoroughly with the Substrate Solution.