產品名稱:牛腫瘤壞死因子α(TNF-α)ELISA Kit
儀器介紹
◆采用一只蓋革-彌勒計數管來測定α、β、γ和X射線輻射 ◆“安全第一”(Safety First)的校準功能能夠避免校準人員的輻射接觸 ◆檢測儀符合歐洲CE認證要求
主要特點
◆內置鹵素淬滅劑GM探測器,對α、β射線源的靈敏度很高 ◆四位液晶顯示,可選擇mR/hr、CPM、mSv/hr、CPS或Total/Timer等單位 ◆總計數/定時器功能對輕微污染進行定時的精確檢測,定時時間可選擇1分鐘-- 24小時
技術參數
◆測量范圍:mR/hr(毫倫/小時):0.001—110.0,CPM(每分鐘計數):0—300,000 μSv/hr(微希伏/小時):0.01—1,100,CPS(每秒鐘計數):0—5,000,總計數: 1—9,999,000 ◆效 率:Sr-90(546kev,2.3MeV βmax)約75% C-14(156kev βmax)約11% Bi-210(1.2MeV βmax)約64% Am-241(5.5MeV α)約36% ◆靈 敏 度:3500CPM/ mR/hr(對于Cs-137) ◆精 度:±15% ◆溫度范圍:-10℃---+50℃ ◆電 源:1節9V堿性電池,電池壽命 200小時◆尺寸重量:150×80×30mm 350克(含電池)
應用領域
◆探測和測定表面沾污◆在操作放射性核素時監測可能存在的放射性暴露量◆調查環境污染◆測定惰性氣體及其它低能放射性核素◆建筑裝飾材料放射測定 射線危害:低劑量的放射性射線輻射(天然背景輻射的變化范圍),對人體無害或風險甚低,但達到一定劑量則會對人體有害,可引起癌癥、白內障、不孕癥、突變、萎縮效應、壽命減短,甚至死亡
應用:
偵測放射性射線,以采取相應防護措施。海關和邊境巡邏,政府執法部門,檢疫檢驗,應急事故處理,核電廠、銀行、政府、實驗室等部門安全巡查,醫學廢料處理,消防隊,采礦業,科學實驗,個人保護,連續監測
參考信息(來自中國輻射防護研究院)
居民的劑量限值為每年1mSv。即0.114μSv/hr。
放射性職業人員劑量限值為每年20mSv,但任何一年不能超過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.
小鼠血漿α顆粒膜蛋白進口原裝,Mouse GMP-140 ELISA Kit檢測報價加樣:.標本為血清:最好將血液先自然存放1-2小時后,再用3000rmp離心15分鐘;標本為血漿:必須使用含抗凝劑的血液標本收集管,采血后必須立即顛倒采血管混合5-10次,放置一段時間后,3000rpm離心15分鐘;若在幾天內檢測,可放在2-8℃冰箱中,若要貯存,則置于-20℃的低溫冰箱內。 2.加樣后及時放入孵箱。 3.加酶試劑后用吸水紙在酶標板表面輕拭吸干。 4.如果采用AT或其他全自動加樣,最好選擇FAME或其他后處理儀器加酶試劑。 5.標本較多時,請分批操作。
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小鼠血漿α顆粒膜蛋白進口原裝,Mouse GMP-140 ELISA Kit檢測報價
DH5α感受態細胞 目錄號:1802
v 產品組成、儲存、穩定性:
儲存:-70 ℃ 保存,避免反復凍融 v 產品介紹: 本公司生產的DH5а感受態細胞是采用大腸桿菌DH5а菌株經特殊工藝處理得到的感受態細胞,可用于DNA 的化學轉化。使用pUC19 質粒檢測,轉化效率可達108 ,-70 ℃ 保存幾個月轉化效率不發生改變。 每支感受態可以酌情分裝使用,降低了實驗的成本。質量穩定,使用方便,質優價廉。 DH5а 菌株的基因型為:F -φ80 lacZΔM15Δ(lacZYA-argF)U169 end A1 recA1 hsdR17(rk -,mk -) sup E44 λ- thi-1 gyrA96 relA1 phoA v 產品特點: 一種用于鋪制與培養質粒平板和粘粒平板的重級缺陷的抑制型株。其φ80 lacZΔM15 基因的產物可與pUC 載體編碼的β-半乳糖苷酶氨基端實現α互補,可用于藍白斑篩選。 |
本試劑盒只能用于科學研究,不得用于醫學診斷,具體說明書請聯系客服索取,本說明書是通用模板,有些數據不準確.產品規格48T/96T 國產/RD進口分裝/TSZ進口原裝工作原理試劑盒采用雙抗體一步夾心法酶聯免疫吸附試驗(ELISA)。往預先包被樣本抗體的包被微孔中,依次加入標本、標準品、HRP標記的檢測抗體,經過溫育并徹底洗滌。用底物TMB顯色,TMB在過氧化物酶的催化下轉化成藍色,并在酸的作用下轉化成最終的黃色。顏色的深淺和樣品中的樣本呈正相關。用酶標儀在450nm 波長下測定吸光度(OD 值),計算樣品濃度。
注意事項1. 試劑盒保存在2-8℃,使用前室溫平衡20分鐘。從冰箱取出的濃縮洗滌液會有結晶,這屬于正常現象,水浴加熱使結晶完全溶解后再使用。2. 實驗中不用的板條應立即放回自封袋中,密封(低溫干燥)保存。3. 濃度為0的S0號標準品即可視為陰性對照或者空白;按照說明書操作時樣本已經稀釋5倍,最終結果乘以5才是樣本實際濃度。4. 嚴格按照說明書中標明的時間、加液量及順序進行溫育操作。5. 所有液體組分使用前充分搖勻。
性能特點1. 準確性:標準品線性回歸與預期濃度相關系數R值,大于等于0.9900。2. 靈敏度:最低檢測濃度小于(參考說明書)3. 特異性:不與其它可溶性結構類似物交叉反應。4. 重復性:板內、板間變異系數均小于15%。5. 貯藏:2-8℃,避光防潮保存。6. 有效期:6個月
免責聲明1. 試劑盒僅供研究使用,不得用于臨床實驗或人體實驗,否則所產生的一切后果,由實驗者承擔,本公司概不負責。 嚴格按照說明書操作,實驗者違反說明書操作,后果由實驗者承擔。本品為科研試劑,只對單位實驗室學校等正規用途出售。如需資料請向客服索取!企業網站:www.yuduobio.com數十萬產品隨親挑選,正規生物公司,可開具正規機打發票。發票需加6個點。
公司介紹
上海羽朵生物科技有限公司生產銷售elisa試劑盒、動物血清、血漿、全血、抗原抗體、金標試劑盒檢測卡、抗血清、生物試劑、培養基、實驗室儀器耗材、化學試劑、生物制品、標準品、對照品、生化免疫制品、免疫親和柱、菌株、質粒、室內質控品、細胞、冰袋、代理進口產品等量大從優!牛血清白蛋白(BSA)1kg 3000元,純度為>99%可定做各種濃度的綿羊紅細胞,兔血紅細胞,雞血紅細胞。出售補體實驗所需的溶血素,試劑盒,蛇毒因子,黃曲霉毒素B1標準品,以色列進口原裝,純度99.8%,1-100mg規格齊全,隨貨帶防偽證書,送檢測試紙。黃曲霉毒素B1標準品,新加坡進口,純度>99%,1-100mg規格齊全,隨貨帶防偽證書,送檢測試紙。另出售環氧化苯并芘標準品,純度99.9%,100mg,500mg,1g三種規格現貨促銷。。。動物血清系列:標準胎牛血清、特級胎牛血清、標準新生牛血清、特級新生牛血清、優級新生牛血清、標準馬血清、特級馬血清、山羊血清、綿羊血清、兔血清、雞血清、大牛血清、小牛血清、豬血清、狗血清、驢血清、豚鼠血清、大鼠血清、小鼠血清、巴比西鼠血清各種動物全血:抗凝全血.脫纖維全血.脫纖維裂解裂解血.抗凝裂解血.各種動物血漿:(胎牛血清、新生牛血漿、大牛血漿、小牛血漿、綿羊血漿、山羊血漿、豬血漿、驢血漿、馬血漿、、狗血漿、兔血漿、大鼠血漿、小鼠血漿、豚鼠血漿)
出售各種真菌毒素類標準品:3-4’苯并芘,環氧化苯并芘、黃曲霉毒素B1,B2,G1,G2,M1,M2、脫氧雪腐鐮刀菌烯酮(DON嘔吐毒素)、3-乙酰基脫氧雪腐鐮刀菌烯醇(3-A-DON)、15-乙酰基脫氧雪腐鐮刀菌烯醇(15-A-DON)、雪腐鐮刀菌烯醇(NIV)、伏馬毒素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、雜色曲霉素、黃曲霉毒素混標液體 (SIGMA)、黃曲霉毒素混標液體 (FERMENTEK)、黃曲霉毒素M1液體標品(10ug/ml)、黃曲霉毒素M1液體標品(0.5ug/ml)、赭曲霉毒素A液體標品、 黃曲霉毒素B1液體標品
實驗室常用試劑(免疫組化/分子試劑盒,生物緩沖液/染色液,核酸/蛋白質Marker,分離試劑)生物制品(核酸及其衍生物,氨基酸/蛋白質,酶/輔酶,維生素/抗生素/激素)等歡迎經銷商代理商洽談合作事宜!本公司誠信經營,如有質量問題可免費退換,請大家放心使用,僅供科研實驗使用,歡迎大家選購!謝謝!如需其他產品請聯系客服索要報價。相關產品推薦:人PL7抗體/抗蘇氨酰tRNA合成酶(PL7)ELISA試劑盒 人PL12抗體/抗丙氨酰tRNA合成酶(PL12/AlaRS)ELISA試劑盒 人抗Mi2抗體(anti-Mi2-Ab)ELISA試劑盒 人抗Ku抗體(anti-Ku-Ab)ELISA試劑盒 人抗IgA抗體(anti-IgA-Ab)ELISA試劑盒 人抗神經元核抗體1型/抗Hu抗體(ANNA-1/Hu)ELISA試劑盒 人抗DNA酶B抗體(anti-DNase B)ELISA試劑盒 人抗BP180抗體(BP180-Ab)ELISA試劑盒 人抗BB抗體(BB-Ab)ELISA試劑盒 人抗平滑肌抗體(ASMA)ELISA試劑盒人抗肝細胞膜抗體(LMA)ELISA試劑盒人抗肝特異性脂蛋白抗體(LSP)ELISA試劑盒人抗眼肌抗體(EMAb)ELISA試劑盒人抗補體1q抗體(C1q)ELISA試劑盒 人抗內因子抗體(IFA)ELISA試劑盒人抗磷脂抗體(Apl/APA)ELISA試劑盒人抗組蛋白抗體(AHA)ELISA試劑盒人晶體蛋白α(Cryα)ELISA試劑盒人晶體蛋白β(Cryβ)ELISA試劑盒 人抗膠原蛋白抗體(CLA)ELISA試劑盒人抗環胍氨酸肽抗體(CCP)ELISA試劑盒人抗核周因子抗體(APF)ELISA試劑盒
運蛋白抗體M57513 0.2ml
Anti-Mfn1 線粒體融合蛋白1抗體M57514 0.1ml
Anti-MGMT O6甲基鳥嘌呤DNA甲基轉移酶抗體M57515 0.1ml
anti-MT 金屬基質硫蛋白抗體M57516 0.1ml
anti-MGr1-Ag/37LRP 層粘連蛋白受體1抗體M575170.2
Anti-MICA 一種細胞應激分子抗體M57518 0.1ml
Anti-Midnolin isoform Protein 1 中腦核仁蛋白1抗體M57519 0.1ml
Anti-Midnolin isoform Protein 2 中腦核仁蛋白2抗體M57520 0.2ml
Anti-MIF 巨噬細胞移動抑制因子抗體M57521 0.1ml
Anti-MIP-1α 巨噬細胞炎癥因子1α抗體M57522 0.1ml
Anti-MIP-1β 巨噬細胞炎癥因子1β 抗體M57523 0.2ml
Anti-MMP-1 基質金屬蛋白酶-1抗體M57524 0.1ml
Anti-MMP-13 基質金屬蛋白酶13抗體M57525 0.1ml
Anti-MMP-14 基質金屬蛋白酶-14抗體M57526 0.1ml
小鼠轉化生長因子α(TGF-α)elisa酶聯免疫檢測試劑盒使用說明書Anti-MMP-2 基質金屬蛋白酶-2抗體M57527 0.1ml
Anti-MMP-3 基質金屬蛋白酶-3抗體M57528 0.1ml
Anti-MMP-7 基質金屬蛋白酶-7抗體M57529 0.1ml
Anti-MMP-9 基質金屬蛋白酶-9抗體M57530 0.1ml
Anti-β-2-MG 鼠抗人β2微球蛋白抗體M57531 0.1ml
Anti-Mo anti-KLH 小鼠抗血藍蛋白抗體M57532 0.2ml
Anti-MOG 髓鞘少樹突膠質細胞糖蛋白抗體M57533 0.2ml
Anti-Mouse anti-human HAS 鼠抗人血清白蛋白單克隆抗體M57534 0.1ml
Anti-Mouse IgA 兔抗小鼠IgA抗體M57535 0.2ml
Anti-MPO 髓過氧化物酶抗體M57536 0.1ml
Anti-MRP1 多藥耐藥相關蛋白1抗體M57537 0.1ml
Anti-MRP2 多藥耐藥相關蛋白2抗體M57538 0.1ml
Anti-MRP3 多藥耐藥相關蛋白3抗體M57539 0.1ml
Anti-MrpL28 線粒體核糖體蛋白L28抗體M57540 1ml
Anti-MSH-2 錯配修復蛋白2抗體M57541 0.1ml
anti-MLH1 錯配修復蛋白1抗體M57542
免費代測 大鼠腫瘤壞死因子α(TNF-α)elisa試劑盒 Y11721A
Y11715A | 大鼠血管內皮細胞粘附分子1(VCAM-1/CD106)Elisa試劑盒 |
Y11716A | 大鼠白介素8(IL-8/CXCL8)Elisa試劑盒 |
Y11717A | 大鼠可溶性核因子κB受體活化因子配基(sRANKL)Elisa試劑盒 |
Y11718A | 大鼠β干擾素(IFN-β/IFNB)Elisa試劑盒 |
Y11719A | 大鼠血小板因子3(PF-3)Elisa試劑盒 |
Y11720A | 大鼠血管內皮細胞生長因子(VEGF)Elisa試劑盒 |
Y11721A | 大鼠腫瘤壞死因子α(TNF-α)Elisa試劑盒 |
免費代測 大鼠腫瘤壞死因子α(TNF-α)Elisa試劑盒 Y11721A
Y11715A | 大鼠血管內皮細胞粘附分子1(VCAM-1/CD106)Elisa試劑盒 |
Y11716A | 大鼠白介素8(IL-8/CXCL8)Elisa試劑盒 |
Y11717A | 大鼠可溶性核因子κB受體活化因子配基(sRANKL)Elisa試劑盒 |
Y11718A | 大鼠β干擾素(IFN-β/IFNB)Elisa試劑盒 |
Y11719A | 大鼠血小板因子3(PF-3)Elisa試劑盒 |
Y11720A | 大鼠血管內皮細胞生長因子(VEGF)Elisa試劑盒 |
Y11721A | 大鼠腫瘤壞死因子α(TNF-α)Elisa試劑盒 |
免費代測 大鼠腫瘤壞死因子α(TNF-α)Elisa試劑盒 Y11721A
上海卒瑞生物科技有限公司是國內專業研發生產Elisa試劑盒、金標檢測試劑盒、酶聯法檢測試劑盒的供應商,且供銷各類生化試劑(進口國產)、培養基、動物血清、抗原、抗體、實驗試劑、人及動物Elisa試劑盒、氨基酸類、實驗室耗材、實驗室儀器、低溫恒溫槽、雪花制冰機、恒溫油槽等各類產品。本公司是專門從事生物科技領域內的技術開發、技術咨詢、銷售為一體的科學技術服務公司。為國內外科研院所、學校、實驗室、制藥、化工、環境保護及衛生檢疫部門等相應企業提供科研實驗技術服務。我們擁有先進的研發技術和雄厚的科學實力,完整、科學的質量管理體系。本公司以誠信、實力和產品質量獲得業界的認可,與多家生產商建立了長期穩定的合作關系。歡迎各界朋友蒞臨參觀、指導和業務洽談。
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