醫(yī)藥級紅沒藥醇原料藥純粉515-69-5 alpha-Bisabololα-紅沒藥醇
紅沒藥醇原料藥純粉515-69-5 alpha-Bisabololα-紅沒藥醇
湖北拓楚慷元醫(yī)藥化工有限公司
http://www.hbtcky.com
紅沒藥醇原料藥純粉515-69-5 alpha-Bisabololα-紅沒藥醇紅沒藥醇原料藥515-69-5 alpha-Bisabololα-紅沒藥醇中文名稱： 紅沒藥醇
紅沒藥醇原料藥515-69-5 alpha-Bisabololα-紅沒藥醇中文別名： 6-甲基-2-（4-甲基-3-環(huán)己烯-1-基）-5-庚烯-2-醇; α-紅沒藥醇 紅沒藥醇原料藥純粉515-69-5 alpha-Bisabololα-紅沒藥醇
紅沒藥醇USP33原料藥515-69-5 alpha-Bisabololα-紅沒藥醇英文名稱： alpha-Bisabolol
紅沒藥醇原料藥515-69-5 alpha-Bisabololα-紅沒藥醇 紅沒藥醇原料藥純粉515-69-5 alpha-Bisabololα-紅沒藥醇紅沒藥醇原料藥純粉515-69-5 alpha-Bisabololα-紅沒藥醇
紅沒藥醇原料藥515-69-5 alpha-Bisabololα-紅沒藥醇CAS號(hào)： 515-69-5
紅沒藥醇原料藥515-69-5 alpha-Bisabololα-紅沒藥醇EINECS號(hào)： 208-205-9
紅沒藥醇原料藥515-69-5 alpha-Bisabololα-紅沒藥醇分子式： C15H26O
紅沒藥醇原料藥515-69-5 alpha-Bisabololα-紅沒藥醇分子量： 222.3663 紅沒藥醇原料藥純粉515-69-5 alpha-Bisabololα-紅沒藥醇
牛腫瘤壞死因子α(TNF-α)ELISA Kit
產(chǎn)品名稱：牛腫瘤壞死因子α（TNF-α）ELISA Kit
Inspector Alert α、β、γ和X射線檢測儀
儀器介紹
◆采用一只蓋革-彌勒計(jì)數(shù)管來測定α、β、γ和X射線輻射 ◆“安全第一”（Safety First）的校準(zhǔn)功能能夠避免校準(zhǔn)人員的輻射接觸 ◆檢測儀符合歐洲CE認(rèn)證要求
主要特點(diǎn)
◆內(nèi)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(jì)數(shù)/定時(shí)器功能對輕微污染進(jìn)行定時(shí)的精確檢測，定時(shí)時(shí)間可選擇1分鐘－－ 24小時(shí)
技術(shù)參數(shù)
◆測量范圍：mR/hr(毫倫/小時(shí))：0.001—110.0，CPM（每分鐘計(jì)數(shù)）：0—300,000 μSv/hr(微希伏/小時(shí))：0.01—1,100，CPS（每秒鐘計(jì)數(shù)）：0—5,000，總計(jì)數(shù)： 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(jié)9V堿性電池，電池壽命 200小時(shí)◆尺寸重量：150×80×30mm 350克（含電池）
應(yīng)用領(lǐng)域
◆探測和測定表面沾污◆在操作放射性核素時(shí)監(jiān)測可能存在的放射性暴露量◆調(diào)查環(huán)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(fēng)險(xiǎn)甚低，但達(dá)到一定劑量則會(huì)對人體有害，可引起癌癥、白內(nèi)障、不孕癥、突變、萎縮效應(yīng)、壽命減短,甚至死亡
應(yīng)用：
偵測放射性射線，以采取相應(yīng)防護(hù)措施。海關(guān)和邊境巡邏，政府執(zhí)法部門，檢疫檢驗(yàn)，應(yīng)急事故處理，核電廠、銀行、政府、實(shí)驗(yàn)室等部門安全巡查，醫(yī)學(xué)廢料處理，消防隊(duì)，采礦業(yè)，科學(xué)實(shí)驗(yàn)，個(gè)人保護(hù)，連續(xù)監(jiān)測
參考信息（來自中國輻射防護(hù)研究院）
居民的劑量限值為每年1mSv。即0.114μSv/hr。
放射性職業(yè)人員劑量限值為每年20mSv，但任何一年不能超過50mSv。
11(α)-甲氧基柴胡皂苷F，104109-37-7
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外觀： 白色粉末規(guī)格： 10mg/支純度： ≥ 98%用途： 用于含量測定/鑒定/藥理實(shí)驗(yàn)等。提取來源： 柴胡溶解性： 溶于甲醇，DMSO，吡啶，不溶于氯產(chǎn)品中文名稱： 11(α)-甲氧基柴胡皂苷F英文名： 11(α)-methoxysaikosaponin FCAS登錄號(hào)： 104109-37-7分子式： C49H82O18CSB-E04547Fe貓α干擾素(IFN-α)ELISA Kit
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(jìn)口原裝,Mouse GMP-140 ELISA Kit檢測
小鼠血漿α顆粒膜蛋白進(jìn)口原裝,Mouse GMP-140 ELISA Kit檢測報(bào)價(jià)加樣:.標(biāo)本為血清：最好將血液先自然存放1-2小時(shí)后，再用3000rmp離心15分鐘；標(biāo)本為血漿：必須使用含抗凝劑的血液標(biāo)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(shí)間后，3000rpm離心15分鐘；若在幾天內(nèi)檢測，可放在2-8℃冰箱中，若要貯存，則置于-20℃的低溫冰箱內(nèi)。 2.加樣后及時(shí)放入孵箱。 3.加酶試劑后用吸水紙?jiān)诿笜?biāo)板表面輕拭吸干。 4.如果采用AT或其他全自動(dòng)加樣，最好選擇FAME或其他后處理儀器加酶試劑。 5.標(biāo)本較多時(shí)，請分批操作。
小鼠血漿α顆粒膜蛋白進(jìn)口原裝,Mouse GMP-140 ELISA Kit檢測報(bào)價(jià)關(guān)鍵詞：北京elisa試劑盒價(jià)格 酶聯(lián)免疫試劑盒價(jià)格 ELISA試劑盒批發(fā)代理 天津ELISA Kit ELISA實(shí)驗(yàn)代做/實(shí)驗(yàn)外包 進(jìn)口原裝HCB試劑盒多少錢 加拿大HCB公司試劑盒說明書 ELISA試劑盒種屬齊全 ELISA血清血漿樣本測定 代做ELISA實(shí)驗(yàn) ELISA試劑盒代測 ELISA實(shí)驗(yàn)原理 elisa特價(jià)銷售 ELISA操作步驟進(jìn)口原裝elisa kit，國產(chǎn)elisa kit，進(jìn)口分裝elisa kit，elisa廠家批發(fā)elisa現(xiàn)貨，elisa試劑盒說明書下載,雙抗夾心elisa測定,
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小鼠血漿α顆粒膜蛋白進(jìn)口原裝,Mouse GMP-140 ELISA Kit檢測報(bào)價(jià)
DH5α感受態(tài)細(xì)胞
| DH5α感受態(tài)細(xì)胞 目錄號(hào)：1802
v 產(chǎn)品組成、儲(chǔ)存、穩(wěn)定性：
儲(chǔ)存：-70 ℃ 保存，避免反復(fù)凍融 v 產(chǎn)品介紹： 本公司生產(chǎn)的DH5а感受態(tài)細(xì)胞是采用大腸桿菌DH5а菌株經(jīng)特殊工藝處理得到的感受態(tài)細(xì)胞，可用于DNA 的化學(xué)轉(zhuǎn)化。使用pUC19 質(zhì)粒檢測，轉(zhuǎn)化效率可達(dá)108 ，－70 ℃ 保存幾個(gè)月轉(zhuǎn)化效率不發(fā)生改變。 每支感受態(tài)可以酌情分裝使用，降低了實(shí)驗(yàn)的成本。質(zhì)量穩(wěn)定，使用方便，質(zhì)優(yōu)價(jià)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(chǎn)品特點(diǎn)： 一種用于鋪制與培養(yǎng)質(zhì)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(chǎn)物可與pUC 載體編碼的β-半乳糖苷酶氨基端實(shí)現(xiàn)α互補(bǔ)，可用于藍(lán)白斑篩選。 |
α-熊果苷
人前列腺素F2α(PGF2α)ELISA試劑盒
本試劑盒只能用于科學(xué)研究，不得用于醫(yī)學(xué)診斷,具體說明書請聯(lián)系客服索取，本說明書是通用模板，有些數(shù)據(jù)不準(zhǔn)確.產(chǎn)品規(guī)格48T/96T 國產(chǎn)/RD進(jìn)口分裝/TSZ進(jìn)口原裝工作原理試劑盒采用雙抗體一步夾心法酶聯(lián)免疫吸附試驗(yàn)（ELISA）。往預(yù)先包被樣本抗體的包被微孔中，依次加入標(biāo)本、標(biāo)準(zhǔn)品、HRP標(biāo)記的檢測抗體，經(jīng)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(zhuǎn)化成藍(lán)色，并在酸的作用下轉(zhuǎn)化成最終的黃色。顏色的深淺和樣品中的樣本呈正相關(guān)。用酶標(biāo)儀在450nm 波長下測定吸光度（OD 值），計(jì)算樣品濃度。
注意事項(xiàng)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(huì)有結(jié)晶，這屬于正，F(xiàn)象，水浴加熱使結(jié)晶完全溶解后再使用。2. 實(shí)驗(yàn)中不用的板條應(yīng)立即放回自封袋中，密封（低溫干燥）保存。3. 濃度為0的S0號(hào)標(biāo)準(zhǔn)品即可視為陰性對照或者空白；按照說明書操作時(shí)樣本已經(jīng)稀釋5倍，最終結(jié)果乘以5才是樣本實(shí)際濃度。4. 嚴(yán)格按照說明書中標(biāo)明的時(shí)間、加液量及順序進(jìn)行溫育操作。5. 所有液體組分使用前充分搖勻。
性能特點(diǎn)1. 準(zhǔn)確性：標(biāo)準(zhǔn)品線性回歸與預(yù)期濃度相關(guān)系數(shù)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(jié)構(gòu)類似物交叉反應(yīng)。4. 重復(fù)性：板內(nèi)、板間變異系數(shù)均小于15%。5. 貯藏：2-8℃，避光防潮保存。6. 有效期：6個(gè)月
免責(zé)聲明1. 試劑盒僅供研究使用，不得用于臨床實(shí)驗(yàn)或人體實(shí)驗(yàn)，否則所產(chǎn)生的一切后果，由實(shí)驗(yàn)者承擔(dān)，本公司概不負(fù)責(zé)。 嚴(yán)格按照說明書操作，實(shí)驗(yàn)者違反說明書操作，后果由實(shí)驗(yàn)者承擔(dān)。本品為科研試劑，只對單位實(shí)驗(yàn)室學(xué)校等正規(guī)用途出售。如需資料請向客服索！企業(yè)網(wǎng)站：www.yuduobio.com數(shù)十萬產(chǎn)品隨親挑選，正規(guī)生物公司，可開具正規(guī)機(jī)打發(fā)票。發(fā)票需加6個(gè)點(diǎn)。
公司介紹
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小鼠轉(zhuǎn)化生長因子α(TGF-α)elisa酶聯(lián)免疫檢測試劑盒使用說明書
運(yùn)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(zhuǎn)移酶抗體M57515 0.1ml
anti-MT 金屬基質(zhì)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(xì)胞應(yīng)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(xì)胞移動(dòng)抑制因子抗體M57521 0.1ml
Anti-MIP-1α 巨噬細(xì)胞炎癥因子1α抗體M57522 0.1ml
Anti-MIP-1β 巨噬細(xì)胞炎癥因子1β 抗體M57523 0.2ml
Anti-MMP-1 基質(zhì)金屬蛋白酶-1抗體M57524 0.1ml
Anti-MMP-13 基質(zhì)金屬蛋白酶13抗體M57525 0.1ml
Anti-MMP-14 基質(zhì)金屬蛋白酶-14抗體M57526 0.1ml
小鼠轉(zhuǎn)化生長因子α(TGF-α)elisa酶聯(lián)免疫檢測試劑盒使用說明書Anti-MMP-2 基質(zhì)金屬蛋白酶-2抗體M57527 0.1ml
Anti-MMP-3 基質(zhì)金屬蛋白酶-3抗體M57528 0.1ml
Anti-MMP-7 基質(zhì)金屬蛋白酶-7抗體M57529 0.1ml
Anti-MMP-9 基質(zhì)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(lán)蛋白抗體M57532 0.2ml
Anti-MOG 髓鞘少樹突膠質(zhì)細(xì)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(guān)蛋白1抗體M57537 0.1ml
Anti-MRP2 多藥耐藥相關(guān)蛋白2抗體M57538 0.1ml
Anti-MRP3 多藥耐藥相關(guān)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(cuò)配修復(fù)蛋白2抗體M57541 0.1ml
anti-MLH1 錯(cuò)配修復(fù)蛋白1抗體M57542
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