13585831301
當(dāng)前位置：上海莼試生物技術(shù)有限公司>>分子生物學(xué)>>細胞培養(yǎng)及檢測>> DMEM/F-12培養(yǎng)基Hyclone使用說明書
DMEM/F-12培養(yǎng)基Hyclone使用說明書*，*，庫存現(xiàn)貨，無效果，免費退款。公司現(xiàn)貨銷售，量大折扣，咨詢。詳細信息如下。
DMEM/F-12培養(yǎng)基Hyclone使用說明書DMEM/F-12培養(yǎng)基Hyclone，DMEM/F-12(1:1)
原裝HycloneSH30023.01
DMEM/F12 1:1培養(yǎng)基 2.50 mM L-谷氨酰胺、15 mM HEPES
DMEM/F-12培養(yǎng)基Hyclone使用說明書分子生物學(xué)領(lǐng)域：
涉及核酸純化、常用分子生物學(xué)試劑、PCR等相關(guān)試劑盒。
分子生物學(xué)試劑：擁有的價格優(yōu)勢，品質(zhì)可信賴，市場占比龐大。
| 產(chǎn)品名稱 | 英文名稱 | 包裝 |
| DMEM/F-12培養(yǎng)基Hyclone使用說明書 | DMEM/F-12 (1:1) | 可根據(jù)客戶要求訂制 |
DMEM/F-12培養(yǎng)基Hyclone使用說明書收貨注意事項：
當(dāng)您收到貨物后，請仔細檢查產(chǎn)品的名稱、數(shù)量、質(zhì)量規(guī)格是否與您訂購產(chǎn)品*。若產(chǎn)生異議，請及時與我司。按照我司指令及時將貨物退回，我司*時間為您安排配送正確貨物。請您務(wù)必保證退還貨物的包裝完整性。
當(dāng)您收到貨物后，若發(fā)現(xiàn)包裝破損，產(chǎn)品泄露等意外情況，請及時拍照留證，并將照片傳回我司，我司確認后，將及時為您更換新的貨物，原有貨物按照我司指令處理。
我司默認貨物簽收24小時內(nèi)無反饋，即視為您已經(jīng)認同我司到貨情況，未出現(xiàn)包裝破損、貨物錯誤等問題。
因大多情況貨物是以快遞形式配送，請盡量本人簽收，如由您認同的其他人或第三方代為簽收，也認同與您本人簽收具有相同的效力，如24小時內(nèi)無反饋，默認貨物完整正確送達。
我司所有產(chǎn)品的質(zhì)量追溯期為90天，若有質(zhì)量異議，請務(wù)必在90天內(nèi)提出，超過90天后，我司默認貴處已經(jīng)認同該產(chǎn)品的質(zhì)量。
type. Progenitor cell layers of skin, breast, eye and prostate express high levels of DeltaN-type isoforms. Isoform 10 is predominantly expressed in skin squamous cell carcinomas, but not in normal skin tissues.
Post-translational modifications : May be sumoylated.
Ubiquitinated. Polyubiquitination involves WWP1 and leads to proteasomal degradation of this protein.
DISEASE : Acro-dermato-ungual-lacrimal-tooth syndrome (ADULT syndrome) [MIM:103285]: A form of ectodermal dysplasia. Ectodermal dysplasia defines a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. ADULT syndrome involves ectrodactyly, syndactyly, finger- and toenail dysplasia, hypoplastic breasts and nipples, intensive freckling, lacrimal duct atresia, frontal alopecia, primary hypodontiaand loss of permanent teeth. ADULT syndrome differs significantly from EEC3 syndrome by the absence of facial clefting. Note=The disease is caused by mutations affecting the gene represented in this entry.
Ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) [MIM:106260]: An autosomal dominant condition characterized by congenital ectodermal dysplasia with coarse, wiry, sparse hair, dystrophic nails, slight hypohidrosis, scalp infections, ankyloblepharon filiform adnatum, maxillary hypoplasia, hypodontia and cleft lip/palate. Note=The disease is caused by mutations affecting the gene represented in CFN99977 http://www.chemfaces。。ｃｏｍ/natural/Pseudoginsenoside-RT5-CFN99977.html C36H62O10 654.88 98474-78-3 Pseudoginsenoside RT5 Triterpenoids >=98% 20mg
CFN99978 http://www.chemfaces。。ｃｏｍ/natural/Ginsenoside-F3-CFN99978.html C41H70O13 770.99 62025-50-7 Ginsenoside F3 Triterpenoids >=98% 10mg
CFN99980 http://www.chemfaces。。ｃｏｍ/natural/Protopanaxatriol-CFN99980.html C30H52O4 476.73 1453-93-6 20(R)-Protopanaxatriol Triterpenoids >=98% 20mg
CFN99983 http://www.chemfaces。。ｃｏｍ/natural/Ciwujianoside-B-CFN99983.html C58H92O25 1189.35 114902-16-8 Ciwujianoside B Triterpenoids >=98% 20mg
CFN99984 http://www.chemfaces。。ｃｏｍ/natural/Eleutheroside-E-CFN99984.html C34H46O18 742.73 39432-56-9 Eleutheroside E Lignans >=98% 20mg
CFN99985 http://www.chemfaces。。ｃｏｍ/natural/Raddeanin-A-CFN99985.html C47H76O16 897.11 89412-79-3 Raddeanin A Triterpenoids >=98% 20mg
DMEM/F-12培養(yǎng)基Hyclone使用說明書CFN98083 http://www.chemfaces。。ｃｏｍ/natural/Vindoline-CFN98083.html C25H32N2O6 456.5 2182-14-1 Vindoline Alkaloids >=98% 20mg
CFN99986 http://www.chemfaces。。ｃｏｍ/natural/Hederasaponin-B-CFN99986.html C59H96O25 1205.4 36284-77-2 Hederasaponin B Triterpenoids >=98% 20mg
請輸入賬號
請輸入密碼
請輸驗證碼
以上信息由企業(yè)自行提供，信息內(nèi)容的真實性、準確性和合法性由相關(guān)企業(yè)負責(zé)，儀表網(wǎng)對此不承擔(dān)任何保證責(zé)任。
溫馨提示：為規(guī)避購買風(fēng)險，建議您在購買產(chǎn)品前務(wù)必確認供應(yīng)商資質(zhì)及產(chǎn)品質(zhì)量。
儀表網(wǎng)