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FKBP14 Protein|FKBP14蛋白質(zhì)|廠家現(xiàn)貨|產(chǎn)品詳情

產(chǎn)品名稱: FKBP14 Protein|FKBP14蛋白質(zhì)|廠家現(xiàn)貨|產(chǎn)品詳情
產(chǎn)品型號(hào): C86-135-22
產(chǎn)品展商: 博飛美科
產(chǎn)品文檔: 無(wú)相關(guān)文檔

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FKBP14 Protein|FKBP14蛋白質(zhì)|廠家現(xiàn)貨|產(chǎn)品詳情由上海創(chuàng)賽科學(xué)儀器有限公司品質(zhì)提供,可查詢FKBP14 Protein價(jià)格。上海創(chuàng)賽科學(xué)儀器有限公司是專業(yè)**試劑生產(chǎn)及供應(yīng)商,其優(yōu)良的品質(zhì)滿足您不同實(shí)驗(yàn)的多種需求,歡迎撥打4006087598洽談選購(gòu),更多產(chǎn)品詳情請(qǐng)登錄www.ahbcpqn.cn


FKBP14 Protein|FKBP14蛋白質(zhì)|廠家現(xiàn)貨|產(chǎn)品詳情  的詳細(xì)介紹

FKBP14蛋白產(chǎn)品信息

別名: FKBP14, FKBP22
表達(dá)方式: 
A DNA sequence encoding the human FKBP14 (Q9NWM8) (Met1-Lys207) was expressed with a polyhistidine tag at the C-terminus.
種屬: Human
表達(dá)宿主: Human Cells

FKBP14 Protein QC Testing

純度: (73.1+25.2) % as determined by SDS-PAGE SDS-PAGE
內(nèi)**: < 1.0 EU per μg of the protein as determined by the LAL method
穩(wěn)定性: Samples are stable for up to twelve months from date of receipt at -70℃
預(yù)測(cè)N端: Ala 20
分子量: 
The recombinant human FKBP14 consists of  199 amino acids and predicts a molecular mass of 22.9 KDa. It migrates as an approximately 25 and 27 KDa band in SDS-PAGE under reducing conditions.
緩沖液: Lyophilized from sterile PBS, pH 7.4.
Normally 5 % - 8 % trehalose and mannitol are added as protectants before lyophilization. Specific concentrations are included in the hardcopy of COA.
Please contact us for any concerns or special requirements.

FKBP14 Protein Usage Guide

儲(chǔ)存方法: Store it under sterile conditions at -70℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
Reconstitution: A hardcopy of COA with reconstitution instruction is sent along with the products. Please refer to it for detailed information.

FKBP14蛋白背景綜述

FKBP14 is a member of the FK506-binding protein family. It contains 2 EF-hand domains and one PPIase FKBP-type domain. Truncation of the amino-terminus of FKBP14 significantly decreases peptidyl prolyl cis-trans isomerase activity, therefore implicating that the PPIase FKBP-type domain must be located at the N-terminus. FKBP14 can be detected in the lumen of the endoplasmic reticulum where it is thought to accelerate the folding of proteins during protein synthesis. Defects in FKBP14 can cause Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss. A syndrome with features of Ehlers-Danlos syndrome types VIA and VIB on the one hand, and the collagen VI-related congenital myopathies Ullrich congenital muscular dystrophy and Bethlem myopathy on the other hand.

參考文獻(xiàn)

Baker K. et al., 2003, Genome Res. 13: 2265-70.
Ota T. et al., 2004, Nat Genet. 36: 40-5.
The MGC Project Team. 2004, Genome Res. 14: 2121-7.

規(guī)格:50ug

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