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硫酸氨基胍CAS:996-19-0
點擊次數(shù):5發(fā)布時間:2016/8/27 20:57:35

更新日期:2016/8/27 20:57:35
所 在 地:中國大陸
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齊一生物專業(yè)代理Sigma西格瑪.美國BD.賽默飛thermofisher.日本wako.TCL.默克Merck .美國AMRESCO.Invitrogen.日本榮研化學株式會社.EP(歐洲藥典).USP(美國藥典).BP(英國藥典)加拿大TRC等試劑.標準品.對照品原裝產(chǎn)品,正品原裝質(zhì)量,貨期短價格優(yōu)惠!歡迎前來選購【硫酸氨基胍CAS:996-19-0】齊一生物科技(上海)有限公司客服熱:400 9910 197/021-6034 8496網(wǎng)站:http://www.qiyibio.com
"硫酸氨基胍CAS:996-19-0 英文名稱:Aminoguanidine hemisulfate salt 規(guī)格:AR,99% 包裝:25克 熔點: 200°C
儲存條件: RT"
5128-1220 Specimen Transport Medium (STM) CE CNY
5123-1220 Female Swab Specimen Collection KitTM CNY
5100-1400IVD hc2 Sample Conversion Kit CNY
EA11424 EASYartus BKV RG_II CNY
5050-1075 V.1 CD Rom Manual, MST Vortexer 2 CNY
EA10124 EASYartus EBV RG PCR Kit 2 CNY
BR-02 DxS B-RAF Mutation Test Kit CNY
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9240719 Cable Carrier, Capper, Elevator, AP CNY
9240701 O-Ring, Shaker, Lower Body, AP96/196 CNY 【硫酸氨基胍CAS:996-19-0】
9240696 Fitting, Barbed, 1/4" ID tube, AP CNY
9243651 Comprehen Valid., QIAgility """The Comprehensive Validation Support plan specific to a laboratory's needs will incorporate all of the requirements for the internal validation guidelines from the FBI's Quality Assurance Standards (QAS).
The Comprehensive Validation Support service includes all travel and labor charges for up to 20 days by the QIAGEN Validation Team. Typically, one week will be required to extract, quantify, and amplify the validation study samples and may require multiple individuals. Usually, two weeks is required to analyze the data and one week to write the final report. The expected time period to complete the Comprehensive Validation is six weeks. The actual time may vary depending on resource availability, including laboratory time dedicated to validation activities.
Lab Work – The QIAGEN specialist(s) will travel to the laboratory to conduct the on-site validation lab work. The QIAGEN specialist team will perform and complete all extractions, quantifications, amplfications, and capillary electrophoresis. The laboratory is responsible for providing systems/protocols that may be needed (generally laboratory SOPs, ex. interpretation guidelines). Additionally, the laboratory staff may be required to provide additional data needed for interpretation (ex. quantification/amplification/CE results) during the data review phase of the validation.
Once the final scope of the validation is determined, QIAGEN will provide a quote for all consumables required for the validation. Non-QIAGEN chemistry and accessories are not included and should be purchased to cover the validation experimental design including qPCR, STR, NIST standards, required samples types (blood, semen, buccal samples) and required substrates (swabs, materials, etc). For planning purposes and to ensure a smooth process, the Customer is expected to have all materials on-hand and inventoried one (1) week prior to the validation start date.
Data Analysis – The Comprehensive Validation Support plan encompasses data collection (quants, amps, CE) during the on-site visit. The laboratory may be responsible for sharing (typically electronically via e-mail) any validation data requested after the on-site visit. A QIAGEN specialist will complete all of the data analysis produced from the validation study design. This includes qPCR (quant) and STR (amp) analysis and linkage to starting samples.
Validation data CD/flashdrive – QIAGEN will review the validation data and draft a validation summary document, ensuring compliance with the FBI's QAS requirements/standards. QIAGEN will send validation data in an electronic format (email/CD/flashdrive) to the laboratory. The laboratory is responsible for final compilation, any format change preferences, review and signoff of the validation report. The documentation provided by QIAGEN will aide in demonstrating compliance with all accreditation guidelines during laboratory audits. Should a hard copy of the validation study be preferred, the laboratory is required to specify prior to the onset of the validation.
Post-validation QIAGEN-to-Laboratory Transfer – Following completion of the validation and generation of the draft validation summary document, a designated member of the QIAGEN validation team will review the validation with the Lab Manager and the Technical Leader. Following sign off on the validation report, training of the laboratory DNA staff will occur. Refer to the Post-validation Competency Training for additional information. """ CNY
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└ 視網(wǎng)膜神經(jīng)節(jié)細胞總DNA 1μg/1μl(10μg/20ug/50ug)
└ 淋巴內(nèi)皮細胞總DNA 1μg/1μl(10μg/20ug/50ug)
└ 淋巴成纖維細胞總DNA 1μg/1μl(10μg/20ug/50ug)
└ 外周血白細胞總DNA 1μg/1μl(10μg/20ug/50ug)
肺大動脈內(nèi)皮細胞 5 × 105 1ml
肺大動脈平滑肌細胞 5 × 105 1ml
肺大靜脈內(nèi)皮細胞 5 × 105 1ml
肺大靜脈平滑肌細胞 5 × 105 1ml
肺動脈成纖維細胞 5 × 105 1ml
肺泡上皮細胞 5 ×105 1ml
氣管上皮細胞 5 × 105 1ml
肺微血管內(nèi)皮細胞 5 × 105 1ml
肺成纖維細胞 5 × 105 1ml
心肌細胞 5 ×105 1ml 【硫酸氨基胍CAS:996-19-0】
心肌成纖維細胞 5 × 105 1ml
主動脈內(nèi)皮細胞 5 × 105 1ml
主動脈平滑肌細胞 5 × 105 1ml
單核細胞 5 × 105 1ml
大隱靜脈平滑肌細胞 5 × 105 1ml
食管上皮細胞 5 × 105 1ml
食管平滑肌細胞 5 × 105 1ml
腸動脈內(nèi)皮細胞 5 × 105 1ml
腸靜脈內(nèi)皮細胞 5 × 105 1ml
腸平滑肌細胞 5 × 105 1ml
腸粘膜上皮細胞 5 × 105 1ml
肝實質(zhì)細胞 5 ×105 1ml
肝動脈內(nèi)皮細胞 5 × 105 1ml
肝動脈平滑肌細胞 5 × 105 1ml
肝內(nèi)膽管上皮細胞 5 × 105 1ml
胃黏膜上皮 5 × 105 1ml 【硫酸氨基胍CAS:996-19-0】
腎實質(zhì)細胞 5 ×105 1ml
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└ 皮膚肥大細胞總DNA 1μg/1μl(10μg/20ug/50ug)
└ 前脂肪細胞總DNA 1μg/1μl(10μg/20ug/50ug)
└ 胰島β細胞總DNA 1μg/1μl(10μg/20ug/50ug)
└ 胰腺星狀細胞總DNA 1μg/1μl(10μg/20ug/50ug)
└ 胰腺導管上皮細胞總DNA 1μg/1μl(10μg/20ug/50ug)
└ 頜下腺上皮細胞總DNA 1μg/1μl(10μg/20ug/50ug)
└ 視網(wǎng)膜微血管內(nèi)皮細胞總DNA 1μg/1μl(10μg/20ug/50ug)
└ 小梁網(wǎng)細胞總DNA 1μg/1μl(10μg/20ug/50ug)
└ 視網(wǎng)膜色素上皮細胞總DNA 1μg/1μl(10μg/20ug/50ug)
└ 視網(wǎng)膜muller細胞總DNA 1μg/1μl(10μg/20ug/50ug)
└ 虹膜色素上皮細胞總DNA 1μg/1μl(10μg/20ug/50ug)
└ 晶狀體上皮細胞總DNA 1μg/1μl(10μg/20ug/50ug) 【異硫氰酸胍CAS:593-84-0】
└ 角膜上皮細胞總DNA 1μg/1μl(10μg/20ug/50ug)
└ 角膜內(nèi)皮細胞總DNA 1μg/1μl(10μg/20ug/50ug)