膠原蛋白雜交肽是3-Hisperson Inc.的產(chǎn)品。膠原蛋白雜交肽(CHP)是一種新型獨特的肽,可在體外和體內(nèi)特異性結(jié)合未折疊的膠原蛋白鏈[1 2 3]。通過共享天然膠原蛋白的Gly-X-Y重復(fù)序列,CHP具有通過以類似于退火至互補(bǔ)DNA鏈的DNA片段的方式重新形成三螺旋結(jié)構(gòu)而與變性膠原蛋白鏈雜交的強(qiáng)能力。CHP非常具體:由于缺乏結(jié)合位點,它對完整的膠原蛋白分子具有可忽略的親和力,并且由于其中性和親水性,它對非特異性結(jié)合是惰性的。CHP是一種強(qiáng)大的組織病理學(xué)工具,能夠直接檢測由多種疾病引起的炎癥和組織損傷以及發(fā)育和衰老期間的組織重塑[3]。CHP可在不使用合成熒光基質(zhì)或遺傳修飾細(xì)胞的情況下,在3D膠原蛋白培養(yǎng)物中通過癌細(xì)胞的蛋白水解遷移而穩(wěn)健地可視化細(xì)胞周基質(zhì)周轉(zhuǎn)[4]。CHP可以在分子水平上測量和定位膠原組織的機(jī)械損傷[5]。它還能夠評估脫細(xì)胞細(xì)胞外基質(zhì)中的膠原蛋白變性[6]。此外,CHP可用于在SDS-PAGE凝膠中特異性顯示膠原蛋白條帶,而無需蛋白質(zhì)印跡[7]。B-CHP用生物素標(biāo)記,用于抗生物素蛋白/鏈霉抗生物素蛋白介導(dǎo)的檢測。B-CHP提供了靈活的檢測選擇,如非綠色熒光和HRP-酶法,以避免背景和增強(qiáng)信號。(目錄號:BIO)用于抗生物素蛋白/鏈霉抗生物素蛋白介導(dǎo)的方法,包括HRP-酶法5-FAM(目錄號:FLU),用于綠色熒光檢測和Cy 3應(yīng)用:免疫熒光免疫組化SDS-PAGE(凝膠內(nèi)蛋白質(zhì)印跡)運輸條件:室溫下以粉末形式快速運輸。儲存:-20 ° C,粉末狀; 4 °C,在水中重構(gòu)后無需分裝和冷凍。在4 °C溶液中穩(wěn)定2年。Publications Powered by Bioz查看Bioz上的更多詳細(xì)信息1)“通過三螺旋肽鏈靶向和模擬膠原蛋白”Curr Opin Chem Biol 2013 17 968- 975. 2)“通過光觸發(fā)三螺旋雜交靶向膠原蛋白鏈”Proceedings of the National Academy of Sciences of the United States of America 2012 109 14767-14772.?DOI:10.1073/pnas.1209721109.3)“用膠原雜交肽進(jìn)行組織重塑的原位成像。ACS Nano 2017 11 9825。DOI:10.1021/acsnano.7b031504)“通過肽雜交可視化膠原蛋白水解:從3D細(xì)胞培養(yǎng)到體內(nèi)成像。“Biomaterials 2018 DOI:10.1016/j.biomerials.2018.08.0395)“膠原雜交肽實現(xiàn)膠原中機(jī)械損傷的分子水平檢測和定位。《國家通訊》 2017 8 14913 DOI:10.1038/ncomms14913.6)“使用膠原雜交肽對脫細(xì)胞組織中的膠原變性進(jìn)行分子評估。生物材料學(xué)報 2017. 53 268-278 DOI:10.1016/j.actbio.2017.01.0797)“Direct detection of collagenous proteins by fluorescently labeled collagen mimetic peptides” Bioconjugate Chemistry 2013 24 9-16. DOI:10.1021/bc3005842.8)“在肌腱中,不同的生理需求導(dǎo)致功能不同的納米結(jié)構(gòu)。“科學(xué)。2018年報告。DOI:DOI:10.1038/s41598-018-22741- 8蛋白酶譜-比酶譜DQ膠原SHG和TEM更信息可靠和方便-對膠原蛋白具有高親和力和無與倫比的特異性,基本上沒有非特異性結(jié)合-適用于所有物種的所有類型的膠原蛋白,依賴于膠原蛋白的二級結(jié)構(gòu),而不是任何定義的結(jié)合序列-適用于冷凍和石蠟包埋切片,無需抗原檢索-一種非抗體方法,對任何共染色抗體沒有物種限制小尺寸(2%的IgG分子量),易于組織滲透和整個標(biāo)本染色,無需切片-在4 °C下的溶液中穩(wěn)定,無需等分儲存
產(chǎn)品描述
The Collagen Hybridizing Peptides are products of 3-Helix Inc.The collagen hybridizing peptide (CHP) is a novel and unique peptide that specifically binds unfolded collagen chains both in vitro and in vivo [1 2 3]. By sharing the Gly-X-Y repeating sequence of natural collagen CHP has a strong capability to hybridize with denatured collagen chains by reforming the triple helical structure in a fashion similar to DNA fragments annealing to complementary DNA strands. CHP is extremely specific: it has negligible affinity to intact collagen molecules due to lack of binding sites and it is inert towards non-specific binding because of its neutral and hydrophilic nature.CHP is a powerful histopathology tool which enables straightforward detection of inflammation and tissue damage caused by a large variety of diseases as well as tissue remodeling during development and aging [3]. CHP robustly visualizes the pericellular matrix turnover caused by proteolytic migration of cancer cells within 3D collagen culture without the use of synthetic fluorogenic matrices or genetically modified cells [4]. CHP can measure and localize mechanical injury to collagenous tissue at the molecular level [5]. It also enables assessment of collagen denaturation in decellularized extracellular matrix [6]. In addition CHP can be used to specifically visualize collagen bands in SDS-PAGE gels without the need for western blot [7]. B-CHP is labeled with biotin for avidin/streptavidin-mediated detection. B-CHP offers flexible detection options such as non-green fluorescence and HRP-enzyme methods to avoid background and enhance signal.CHP come in three varieties: labeled with biotin (Catalog #: BIO) for avidin/streptavidin-mediated including HRP-enzyme methods 5-FAM (Catalog #: FLU) for green fluorescence detection and Cy3 (Catalog #: RED) for red fluorescence detection.Applications: immunofluorescence immunohistochemistry SDS-PAGE (in-gel Western blot)Shipping Conditions: Express shipping as powder at ambient temperature. Store at -20 ?°C upon arrival until use.Storage: -20 ?°C as powder; 4 ?°C after reconstitution in water no need to aliquot and freeze. Stable for 2 years in solution at 4 ?°C.Publications Powered by Bioz See more details on Bioz1) a€?Targeting and mimicking collagens via triple helical peptide assembliesa€? Curr Opin Chem Biol 2013 17 968-975.2) a€?Targeting collagen strand by photo-triggered triple-helix hybridizationa€? Proceedings of the National Academy of Sciences of the United States of America 2012 109 14767-14772. DOI: 10.1073/pnas.1209721109.3) "In situ imaging of tissue remodeling with collagen hybridizing peptides." ACS Nano 2017 11 9825. DOI: 10.1021/acsnano.7b031504) "Visualizing collagen proteolysis by peptide hybridization: From 3D cell culture to in vivo imaging." Biomaterials 2018 DOI:10.1016/j.biomaterials.2018.08.0395) "Molecular level detection and localization of mechanical damage in collagen enabled by collagen hybridizing peptides." Nat. Commun. 2017 8 14913 DOI: 10.1038/ncomms14913.6) "Molecular assessment of collagen denaturation in decellularized tissues using the collagen hybridizing peptide." Acta Biomater. 2017. 53 268-278 DOI: 10.1016/j.actbio.2017.01.0797) a€?Direct detection of collagenous proteins by fluorescently labeled collagen mimetic peptidesa€? Bioconjugate Chemistry 2013 24 9-16. DOI: 10.1021/bc3005842.8) "In tendons differing physiological requirements lead to functionally distinct nanostructures." Sci. Reports 2018. DOI: DOI:10.1038/s41598-018-22741-8Features-More informative reliable and convenient than zymography DQ collagen SHG and TEM-High affinity and unparalleled specificity to collagen with essentially no nonspecific binding-Applicable to all types of collagen from all species relying on collagen's secondary structure instead of any defined sequence for binding-Suitable for both frozen and paraffin-embedded sections with no need for antigen retrieval-A non-antibody approach with no species restrictions against any co-staining antibodySmall size (2% of IgG by MW) enabling facile tissue penetration and whole specimen staining without sectioning-Stable in solution under 4 ?°C eliminating the need to aliquot for storage