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.
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技術(shù)參數(shù) | |||
通道數(shù)量 | 96 | 通道間隔 | 50GHz, 100GHz |
通道頻率 | 196.45~191.7THz | 最大輸入功率 | 500mW; 27dBm |
帶寬 | 1526.05~1563.86 nm | 光源接頭 | SC/PC Standard |
測量速度 | 4 Sec. (all 96ch.) | 電池 | 鋰聚合物電池, 1800毫安時,3.7伏 |
測量范圍 | +10~-40dBm | 電池工作時長 | 充滿電后單次使用620分鐘 |
測量精度 | ± 1.0dB @ -40 dBm | 電流消耗(Max) | 0.25A |
顯示屏分辨率 | 0.01dB | 電力消耗 | 0.925W |
顯示單位 | dB, dBm,nm,THz | 顯示 | 3.5” TFT-LCD, 16bit color, 240*320 |
重量 | 0.6 kg | 尺寸 | 196*95*40 mm |
溫度 (環(huán)境條件) | -20 to +55 °C (操作環(huán)境) | 濕度 (最大無冷凝) | 95% (操作環(huán)境) |
-35 to +65°C (儲存環(huán)境) | 85% (儲存環(huán)境) |
BQF16-15型風(fēng)動潛水泵
該泵以壓縮空氣為動力,采用離心泵結(jié)構(gòu)形式。
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eppendorf艾本德離心機5810/5810R產(chǎn)品簡介
eppendorf艾本德離心機5810/5810R系列離心機適用于實驗室中等通量至高通量的離心應(yīng)用。該系列離心機結(jié)合卓越多功能和高通量離心為一體,可以離心幾乎所有市面上通用的離心管和工作板,而離心機的占地面積卻很小。通過不斷更新技術(shù),5810和5810R離心機的最大容量已經(jīng)提升到 4 × 750 mL(或是28x50mL / 56x15mL)。由于占地面積小,5810/5810 R 是目前最精巧的 3L 級臺式離心機。
訂購電話14792289446
eppendorf艾本德離心機5810R產(chǎn)品特點:
· 水平吊籃和適配器,適用于0.2 mL至750 mL離心應(yīng)用
· 工作板轉(zhuǎn)子適用于離心各類微孔板、PCR板、細胞培養(yǎng)板和深孔板
· 固定角轉(zhuǎn)適用于分子生物學(xué)高速離心應(yīng)用,可以離心0.2mL至85mL的離心管
· 相對離心力高達20,913 × g(轉(zhuǎn)速 14,000 rpm)
· 獨有QuickLock®氣密性快速鎖定轉(zhuǎn)子蓋和吊籃蓋,便于單手快速鎖定轉(zhuǎn)子和吊籃,特別適合危險樣品的離心,如病原菌、病毒、 血液樣品以及放射性樣品
· 輕輕一按即可關(guān)閉離心機蓋
· 開蓋高度低僅為29cm,便于取放樣品
· 靜音操作,提供舒適的實驗室環(huán)境
· 占地面積小,節(jié)省了有限的實驗室空間
· 自動轉(zhuǎn)子識別和自動失衡檢測,確保離心安全
· 溫度控制范圍:-9 °C至 40 °C
· FastTemp 快速預(yù)冷功能
· Standby cooling 待機冷卻功能,可使轉(zhuǎn)子腔在待機狀態(tài)下維持設(shè)定溫度
· ECO 自動待機功能,8 小時不使用自動待機,節(jié)約能耗,延長壓縮機使用壽命
· 動態(tài)壓縮機控制技術(shù)(DCC),優(yōu)化制冷性能
eppendorf艾本德離心機5810/5810R技術(shù)參數(shù):
型號 | 5810 型離心機 | 5810 R冷凍離心機 |
最大相對離心力 | ||
固定角轉(zhuǎn) | 20,913 x g | 20,913 x g |
水平轉(zhuǎn)子 | 4,500 x g | 4,500 x g |
工作板轉(zhuǎn)子 | 3,486 x g | 3,486 x g |
最高轉(zhuǎn)速 | 200–14,000 rpm (以 10 rpm 遞增) | |
最大容量 | 4 x 750 ml | 4 x 750 ml |
轉(zhuǎn)子數(shù) | 18 | 18 |
加速/減速檔 | 10/10 | 10/10 |
程序 | 35 個用戶程序 | 35 個用戶程序 |
離心計時 | 1 分鐘至99分鐘,可以連續(xù)離心,具備short spin瞬時離心功能 | |
溫控范圍 | –9 °C 至 40 °C | |
噪音水平:S-4-104水平轉(zhuǎn)子 (4x750 mL) | <70 dB(A) | <56 dB(A) |
噪音水平:FA-45-6-30 固定角轉(zhuǎn)(6x50 mL) | <56 dB(A) | <55 dB(A) |
電源 | 230 V/50–60 Hz | 230 V/50–60 Hz |
功率 | 最大 900 W | 最大 1,650 W |
尺寸 (長 x 寬 x 高) | 54 x 61 x 35 cm | 70 x 61 x 35 cm |
開蓋高度 | 80 cm | 80 cm |
重量(不含轉(zhuǎn)子) | 68 kg |
通風(fēng)柜:全鋼通風(fēng)柜; 鋼材:上海寶鋼1.2mm厚防靜電腐蝕噴塑處理; 臺面材質(zhì):美國威盛亞實芯理化板; 風(fēng)機:配備通風(fēng)柜所用風(fēng)量; 玻璃層板:10mm厚耀華鋼化玻璃; 配件:絞鏈滑軌為德國進口; 顏色:待定
MC-3000B/S系列涂鍍層測厚儀
產(chǎn)品概述:
MC-3000B/S涂層測厚儀,它能快速、無損傷、精密地進行涂、鍍層厚度的測量。既可用于實驗室,也可用于工程現(xiàn)場。通過使用不同的測頭,還可滿足多種測量的需要。本儀器能廣泛地應(yīng)用在制造業(yè)、金屬加工業(yè)、化工業(yè)、商檢等檢測領(lǐng)域。是材料保護專業(yè)必備的儀器。本儀器符合以下標準: GB/T 4956─1985 磁性金屬基體上非磁性覆蓋層厚度測量 磁性方法 GB/T 4957─1985 非磁性金屬基體上非導(dǎo)電覆蓋層厚度測量 渦流方法 JB/T 8393─1996 磁性和渦流式覆層厚度測量儀 JJG 889─95 《磁阻法測厚儀》 JJG 818─93 《電渦流式測厚儀》。
功能特點:
●采用了磁性和渦流兩種測厚方法,可無損地測量磁性金屬基體(如鋼、鐵、合金和硬磁性鋼等)上非磁性覆層的厚度(如鋅、鋁、鉻、銅、橡膠、油漆等)及非磁性金屬基體(如銅、鋁、鋅、錫等)上非導(dǎo)電覆層的厚度導(dǎo)電金屬基體(如:橡膠、油漆、塑料、陽極氧化膜等)。
●可使用6 種測頭(F0.5,F(xiàn)1.2,F(xiàn)3,F(xiàn)5,F(xiàn)9,N1.2)
●具有溫度補償功能:配有科電最新“鎖相環(huán)”技術(shù)
●具有屏幕翻轉(zhuǎn)功能:可以手動選擇翻轉(zhuǎn)顯示測量數(shù)據(jù)
●測量速度:根據(jù)不同的應(yīng)用場合客戶可以選擇單次測量和連續(xù)測量兩種測量速度
●顯示方式:2.4寸TFT高清彩屏,320*240像素,大號數(shù)字顯示。
●可采用三種方法對儀器進行校準,并可用基本校準法對測頭的系統(tǒng)誤差進行修正
●具有存儲功能:可以存儲超過1萬個測量點
●具有刪除功能:可以刪除存儲組中的一個可疑數(shù)據(jù),也可以刪除所有的存儲數(shù)據(jù),以便進行新的測量
●設(shè)置限界:對限界外的測量值能自動報警;并可用直方圖對一批測量值進行分析
●顯示語言:內(nèi)置中文、英文
●測量單位:公制、英制可轉(zhuǎn)換
●具有打印功能:可以連接藍牙打印機,打印測量數(shù)據(jù)
●具有無線通信功能:藍牙2.0,可以與電腦和打印機進行無線通信
●具有電源欠壓指示功能
●操作過程有蜂鳴聲提示
●設(shè)有兩種關(guān)機方式:手動關(guān)機方式和自動關(guān)機方式
●V型槽:人性的V型槽結(jié)構(gòu)方便測量各種尺寸管道外表面的涂層
●大平底:專用的大平底探頭結(jié)構(gòu)使儀器測量更加穩(wěn)定,重復(fù)性更高
●防滑墊:專業(yè)設(shè)計的防滑墊配合機殼背面的防滑紋理使客戶長時間操作也不易疲勞,體現(xiàn) 了科電客戶至上的一貫理念
MC-3001全分體式通用型涂層測厚儀
MC-3001全分體式通用型涂層測厚儀是在MC-3000B/S系列的基礎(chǔ)上升級的一款全量程、多功能的分體涂鍍層測厚儀。它可以配置科電儀器的所有分體探頭,一臺主機既可以使用磁性探頭,又可以使用非磁性探頭,也可以選擇內(nèi)防腐探頭等各種定制探頭。用戶根據(jù)需要可以選擇一只或者多只探頭進行任意匹配;根據(jù)探頭的型號不同,對應(yīng)的測量范圍,測量材料也相應(yīng)不同。
MC-3000B/S & MC-3001系列涂鍍層測厚儀
功能介紹:
測頭類型 | 可選見探頭附表 | |
測量模式 | 精簡模式、監(jiān) 探模式、統(tǒng)計模式、最小值捕捉 | |
測量原理 | 磁感應(yīng)和電渦流 | |
測量范圍 | 探頭決定 | |
探頭連接方式 | MC-3000B | 一體式內(nèi)置探頭(不可更換) |
MC-3000S | 分體式導(dǎo)線連接(不可更換) | |
MC-3001 | 分體式導(dǎo)線連接(任意匹配) | |
溫度補償 | 配有科電最新“鎖相環(huán)”技術(shù) | |
語言 | 內(nèi)置中文、英文 | |
顯示方式 | 2.4寸TFT高清彩屏,320*240像素,大號數(shù)字顯示,支持翻轉(zhuǎn)顯示。 | |
測量速度 | 根據(jù)不同的應(yīng)用場合客戶可以選擇單次測量和連續(xù)測量兩種測量速度 | |
數(shù)據(jù)接口 | 藍牙2.0,可以與電腦和打印機進行無線通信 | |
存儲方式 | 手動存儲、自動存儲可選,存儲容量超過一萬個讀數(shù)。 | |
校準方式 | 基本校準、系統(tǒng)校準、一點校準 | |
日歷 | 可以顯示時間信息,,也可以讓存儲的數(shù)據(jù)帶上時間具有可追溯性 | |
單位 | 公制、英制可轉(zhuǎn)換 | |
電源 | 兩節(jié)五號(AA)電池 | |
使用溫度 | 相對濕度:≤90% ; 溫度:-10℃~+40℃ | |
主機尺寸 | 150mm(L)*68mm(W)*33mm(H) | |
重量 | 220g(含電池) |
MC-3000B/S & MC-3001涂層測厚儀探頭型號:
探頭型號 | F0.5 | F1.2 | F3 | F5 | F9 | N1.2 |
測量原理 | 磁感應(yīng) | 電渦流 | ||||
測量范圍 | 0-0.5mm | 0-1.25mm | 0-3mm | 0-5mm | 0-9mm | 0-1.25mm |
分辨率(μm) | 0.1 | 0.1 | 0.1 | 10 | 10 | 0.1 |
誤差 | ±(1~3% )H±1或H±2μm注:H為被測覆層的厚度值 | |||||
顯示精度 | 0~100μm: 0.1μm; 100~999μm: 1μm; 1mm~9mm: 0.01mm | |||||
基體最小平面直徑 | 6mm | 9mm | 12mm | 20mm | 20mm | 9mm |
最小曲率半徑(凹) | 5mm | 6mm | 7.5mm | 10mm | 10mm | 6mm |
最小曲率半徑(凸) | 1.5mm | 1.5mm | 2mm | 5mm | 5mm | 1.5mm |
3000系列涂層測厚儀還配有科電獨自研發(fā)的“鎖相環(huán)”技術(shù)。“鎖相環(huán)”技術(shù)技術(shù)的產(chǎn)生一舉打破了國外產(chǎn)品該技術(shù)對中國的壟斷。該技術(shù)大大減少了工作環(huán)境溫度變化和干擾對儀器的影響,精確性、重復(fù)性也因此大幅度提升。其中3000A的最高分辨率為0.1um,重復(fù)性1%,60um以內(nèi)的電鍍層僅有1~2um誤差,現(xiàn)場測量的絕大多數(shù)工件無需校準直接測量。另外,為了配合不同尺寸、不同形狀的涂、鍍層工件,科電儀器還專門設(shè)計了不同型號的內(nèi)防腐探頭,以滿足客戶的一些特殊需求。
KEM自動滴定儀AT-710系列KEM自動滴定儀AT-710系列主要特點:AT-710M:觸摸屏和操作單元之間無線連接,同時控制四臺自動滴定測量單元。通過使用無線適配器(藍牙),操作單元和滴定裝置可以不用電纜連接。在測量樣品過程中有危害性氣體時,可將滴定裝置放置在排煙柜中,由無線傳輸?shù)牟僮鲉卧獔?zhí)行滴定。AT-710M/AT-710S:滴定劑的信息存儲在滴定管上的芯片中。即使滴定管單元轉(zhuǎn)移到另一個滴定裝置,也不需要重新輸入滴定劑信息。AT-710M/AT-710S/AT-710B:滴定管單元特殊的開關(guān)閥門。減少滴定管和開關(guān)閥門間的死體積。特殊結(jié)構(gòu)的設(shè)計可減少滴定劑的使用量和快速更換滴定單元。AT-710M/AT-710S/AT-710B:智能化電極電纜。電極的信息可透過電纜上傳感器存儲相關(guān)資料。電極校準的數(shù)據(jù)可應(yīng)用到不同的自動滴定儀上。KEM自動滴定儀AT-710系列技術(shù)參數(shù):
名稱 | 自動電位滴定儀 | ||
儀器型號 | AT-710M | AT-710S | AT-710B |
儀器組成 | MCU-710M+AT-710+螺旋槳或磁力攪拌器 | MCU-710S+AT-710+螺旋槳或磁力攪拌器 | AT-710+螺旋槳或磁力攪拌器 |
測量范圍 | 1)電位: -2000.0~2000.0mV2) pH: -20.000~20.000pH3)溫度: 0~100°C | ||
滴定方式 | 自動滴定,自動間歇滴定,間歇滴定,恒pH滴定 | ||
石油中和值滴定,COD滴定 | |||
滴定類型 | 電位滴定(酸堿,氧化還原,沉淀),光度滴定,極化滴定,電導(dǎo)滴定 | ||
終點判斷 | 全量滴定(自動終點),自動終點滴定,設(shè)定終點滴定 | ||
交叉點滴定,自動終點/設(shè)定終點滴定 | |||
特殊應(yīng)用 | 量電極電位(pH, mV),酸解離常數(shù)(pKa) | ||
同時記錄雙通道電位,學(xué)習(xí)滴定 | |||
輸入設(shè)置 | 觸摸屏輸入 | 按鍵輸入 | |
顯示 | 1) 8.4英寸彩色液晶屏,800x600點 | 1) LED背景光源液晶屏 | |
2)英文/日文/中文/韓文/俄文/西語/德語/法語 | 2)英文/日文/中文/韓文/俄文/西語 | ||
3)四個通道同時顯示 | 3)一個通道顯示 | 3)一個通道顯示 | |
計算 | 濃度計算,統(tǒng)計計算(平均值,標準差,相對標準差),自動輸入空白和滴定度 | ||
數(shù)據(jù)儲存 | 500組樣品結(jié)果 | 50組樣品結(jié)果 | |
GLP認證 | 登記操作者/使用群組管理滴定劑:提示滴定度測量日期/指示滴定劑剩余量/提示滴定管活塞更換日期/提示滴定劑換日期/滴定度測量履歷性能檢查:提醒計劃檢查日期/記錄檢查結(jié)果電極管理:記錄校正日期/記錄校正履歷/電極檢查/電極檢查履歷滴定管驗證:驗證/記錄驗證結(jié)果時間管理:顯示操作時間 | 登記操作者/記錄檢查結(jié)果/電極校正記錄/滴定管精度確認/時間管理 | |
滴定管單元 | 20mL玻璃滴定管附褐色保護套(標配),選配: 10mL,5mL或1mL | ||
滴定管精確度 | 50mL滴定管(自動注入器): ±0.5mL20mL滴定管: 0.02mL 重復(fù)性: 0.01mL10mL滴定管: 0.015mL 重復(fù)性: 0.005mL5mL滴定管: 0.01mL 重復(fù)性: 0.003mL1mL滴定管: 0.005mL 重復(fù)性: 0.001mL | ||
擴大器 | 1) STD: pH(mV), mV,雙通道(標配)2) PTA: pH(mV), mV,光度,三通道3) POA: pH(mV), mV,極化,三通道4) CMT: pH(mV), mV,電導(dǎo),三通道5) TET: pH(mV),pH(mv), mV,三通道 | ||
外部輸出 | RS-232C x3 | RS-232C x 2 | |
打印機,電子天平,數(shù)據(jù)軟件(SOFT-CAP) | |||
USB x; 1 | USB x 1 | ||
U盤,熱敏打印機,A4打印機,鍵盤, 條碼機,腳踏開關(guān), USB集線器 | U盤,熱敏打印機,鍵盤,條碼機,腳踏開關(guān), USB集線器,安卓設(shè)備 | ||
LAN x 1 :電腦(PC) | |||
擴充功能 | 測量單元:電位滴定儀(AT-710)容量水分儀(MKV-710)庫侖水分儀MKC-710)最多四臺測量單元 | ||
自動活塞滴定管:最多可控制10臺滴定管驅(qū)動單元(包括主機兩臺) | |||
多樣品自動進樣器: CHA-600,CHA-700 | CHA-700 | ||
使用環(huán)境 | 1)溫度: 5~35°C2)相對濕度: 85%RH以下 | ||
電源 | AC100~240V,50Hz/60Hz | ||
耗電量 | 主機:約30瓦打印機:約7瓦 | 主機:約20瓦打印機:約7瓦 | |
尺寸 | 觸摸屏: 225(W) x 190(D) x 42(H)mm | ||
滴定單元: 141(W) x 296(D) x 367(H)mm(不包括管路)打印機: 106(W) x 180(D) x 88(H)mm | |||
重量 | 觸摸屏:約1.5公斤 | ||
滴定單元:約4.0公斤打印機:約0.4公斤 |