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維生素C鈉CAS:134-03-2
點(diǎn)擊次數(shù):25發(fā)布時(shí)間:2016/8/25 21:58:32

更新日期:2016/8/25 21:58:32
所 在 地:中國大陸
產(chǎn)品型號:
優(yōu)質(zhì)供應(yīng)
詳細(xì)內(nèi)容
齊一生物長期出售上萬種進(jìn)口試劑.對照品.藥物雜質(zhì).中檢所對照品.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(xué)株式會(huì)社.EP(歐洲藥典).USP(美國藥典).BP(英國藥典).加拿大TRC.美國CaTO.標(biāo)準(zhǔn)品.對照品等保證原裝產(chǎn)品,原裝質(zhì)量.到貨快捷安全,專業(yè)的物流配送,專人全程跟蹤訂單,確保貨物安全.準(zhǔn)確.及時(shí)地送達(dá)指定地點(diǎn). 【維生素C鈉CAS:134-03-2】
歡迎咨詢電話:021-6034 8467/6034 8496;
"維生素C鈉CAS:134-03-2 英文名稱:Sodium ascorbate 規(guī)格:AR,99% 包裝:25克 儲(chǔ)存條件: RT,避光
溶解性: 易溶于水
介紹: 無嗅,稍帶咸味。其水溶液當(dāng)pH值>6時(shí)不穩(wěn)定,會(huì)很快被空氣氧化。水中溶解度:620 g/l (20°C); 溫水: 78 g/100ml。"
QYS-03248 紅霉素-N-脫甲基酶ERND測試盒 100管/48樣 酶標(biāo)法
QYS-03249 細(xì)胞色素b5含量測試盒 50管/48樣 可見分光光度法
QYS-03250 細(xì)胞色素b5含量測試盒 100管/96樣 酶標(biāo)法
QYS-03251 血鉀濃度測試盒 50管/48樣 可見分光光度法
QYS-03252 血鉀濃度測試盒 100管/96樣 酶標(biāo)法
QYS-03253 血鈣濃度測試盒 50管/48樣 可見分光光度法
QYS-03254 血鈣濃度測試盒 100管/96樣 酶標(biāo)法
QYS-03255 血清鐵濃度測試盒 50管/48樣 可見分光光度法
QYS-03256 血清鐵濃度測試盒 100管/96樣 酶標(biāo)法
QYS-03257 血鎂濃度測試盒 50管/48樣 可見分光光度法 【維生素C鈉CAS:134-03-2】
QYS-03258 血鎂濃度測試盒 100管/96樣 酶標(biāo)法
QYS-03259 血磷濃度測試盒 50管48樣 可見分光光度法
QYS-03260 血磷濃度測試盒 100管/96樣 酶標(biāo)法
QYS-03261 血鈉濃度測試盒 50管/48樣 可見分光光度法
QYS-03262 血鈉濃度測試盒 100管/96樣 酶標(biāo)法
QYS-03263 血清總鐵結(jié)合能力測試盒 50管/48樣 可見分光光度法
QYS-03264 血鋅濃度測試盒 50管/48樣 可見分光光度法
QYS-03265 血鋅濃度測試盒 100管/96樣 酶標(biāo)法
QYS-03266 水樣中汞離子Hg2+濃度測試盒 50管/48樣 可見分光光度法
QYS-03267 水樣中六價(jià)鉻離子Cr6+濃度測試盒 50管/48樣 可見分光光度法
QYS-03268 組織無機(jī)磷含量測試盒 50管/48樣 可見分光光度法
QYS-03269 組織無機(jī)磷含量測試盒 100管/96樣 酶標(biāo)法
QYS-03270 組織總磷含量測試盒 50管/48樣 可見分光光度法
QYS-03271 組織總磷含量測試盒 100管/96樣 酶標(biāo)法
QYS-03272 土壤汞S-Hg濃度測試盒 50管/48樣 可見分光光度法
QYS-03273 土壤無機(jī)磷S-PHOS含量測試盒 50管/48樣 可見分光光度法 【維生素C鈉CAS:134-03-2】
QYS-03274 土壤總磷/有機(jī)磷/無機(jī)磷含量測試盒 50管/24樣 可見分光光度法
QYS-03275 土壤脲酶UE測試盒 50管/24樣 可見分光光度法
QYS-03276 土壤多酚氧化酶PPO測試盒 50管/48樣 可見分光光度法
QYS-03277 土壤β-葡萄糖苷酶β-GC測試盒 50管/24樣 可見分光光度法
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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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