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recombinant human cadherin 20  (R&D Systems)


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    Structured Review

    R&D Systems recombinant human cadherin 20
    Recombinant Human Cadherin 20, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/recombinant human cadherin 20/product/R&D Systems
    Average 93 stars, based on 1 article reviews
    recombinant human cadherin 20 - by Bioz Stars, 2026-04
    93/100 stars

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    A) Western blot of in vitro cleavage of recombinant cadherin with purified 3CLPro. 1uM of purified 3CLPro was incubated with 2ug of recombinant CDH6 or <t>CDH20</t> (C-terminal His-Tag) in a 50uL reaction for 1hr. Shown are cleavage sites within the recombinant fragment, with amino acid positions displayed for the full length proteins. Western blots showing staining against the C-terminus (His-Tag) of each protein and 3CLPro. Recombinant proteins are a mixture of glycosylated (∼90kDa) and unglycosylated (∼65kda), corresponding to cleavage fragments of ∼62kDa and 40kDa (respectively). B) Western blot of in vitro cleavage of purified human alpha thrombin (IIa). Diagram shows amino acid position of unprocessed prothrombin. Position of cleavage site shown with respect to epitope of antibody used for western blot. 1uM of purified 3CLpro was incubated with 2ug alpha thrombin overnight under reducing conditions, with or without the 3CLPro inhibitor GC376 (1uM). C) In vitro cleavage of purified recombinant NOTCH1 fragment (aa2280-2550) with a N-terminal His-Tag. Reactions were done with 1uM of purified 3CLPro for 1hr. Diagram shows position of cleavage within the NOTCH1 fragment, with amino acid positions corresponding to the full length protein. Epitope regions showed for antibody with epitope C-terminal to the cleavage site. Full length size is ∼29kDa, with N and C-terminal fragments of 4kDa and 25kDa (respectively). D) Cellular cleavage of NOTCH1. Western blots show lysates of hIPSC cardiomyocytes expressing 3CLPro or catalytically inactive C145A variant for 48h. Cleavage site position within the intracellular fragment of NOTCH1 shown, as well as epitope for antibody used in western blot. For all statistics shown, * = p ≤ 0.05 , ** p ≤ 0.01, ***p ≤ 0.001, **** = p ≤ 0.00001
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    R&D Systems cadherin 20 cdh20
    The full list of ECM proteins and conditions that are used in the MEMA experiments. The uniprot ID, stock concentrations, and final working concentrations are provided. In some instances, the printed condition represents a protein complex or a combination of multiple proteins, which is indicated in the notes column.
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    A) Western blot of in vitro cleavage of recombinant cadherin with purified 3CLPro. 1uM of purified 3CLPro was incubated with 2ug of recombinant CDH6 or CDH20 (C-terminal His-Tag) in a 50uL reaction for 1hr. Shown are cleavage sites within the recombinant fragment, with amino acid positions displayed for the full length proteins. Western blots showing staining against the C-terminus (His-Tag) of each protein and 3CLPro. Recombinant proteins are a mixture of glycosylated (∼90kDa) and unglycosylated (∼65kda), corresponding to cleavage fragments of ∼62kDa and 40kDa (respectively). B) Western blot of in vitro cleavage of purified human alpha thrombin (IIa). Diagram shows amino acid position of unprocessed prothrombin. Position of cleavage site shown with respect to epitope of antibody used for western blot. 1uM of purified 3CLpro was incubated with 2ug alpha thrombin overnight under reducing conditions, with or without the 3CLPro inhibitor GC376 (1uM). C) In vitro cleavage of purified recombinant NOTCH1 fragment (aa2280-2550) with a N-terminal His-Tag. Reactions were done with 1uM of purified 3CLPro for 1hr. Diagram shows position of cleavage within the NOTCH1 fragment, with amino acid positions corresponding to the full length protein. Epitope regions showed for antibody with epitope C-terminal to the cleavage site. Full length size is ∼29kDa, with N and C-terminal fragments of 4kDa and 25kDa (respectively). D) Cellular cleavage of NOTCH1. Western blots show lysates of hIPSC cardiomyocytes expressing 3CLPro or catalytically inactive C145A variant for 48h. Cleavage site position within the intracellular fragment of NOTCH1 shown, as well as epitope for antibody used in western blot. For all statistics shown, * = p ≤ 0.05 , ** p ≤ 0.01, ***p ≤ 0.001, **** = p ≤ 0.00001

    Journal: bioRxiv

    Article Title: Prediction and validation of host cleavage targets of SARS-CoV-2 3C-like protease

    doi: 10.1101/2022.01.17.476677

    Figure Lengend Snippet: A) Western blot of in vitro cleavage of recombinant cadherin with purified 3CLPro. 1uM of purified 3CLPro was incubated with 2ug of recombinant CDH6 or CDH20 (C-terminal His-Tag) in a 50uL reaction for 1hr. Shown are cleavage sites within the recombinant fragment, with amino acid positions displayed for the full length proteins. Western blots showing staining against the C-terminus (His-Tag) of each protein and 3CLPro. Recombinant proteins are a mixture of glycosylated (∼90kDa) and unglycosylated (∼65kda), corresponding to cleavage fragments of ∼62kDa and 40kDa (respectively). B) Western blot of in vitro cleavage of purified human alpha thrombin (IIa). Diagram shows amino acid position of unprocessed prothrombin. Position of cleavage site shown with respect to epitope of antibody used for western blot. 1uM of purified 3CLpro was incubated with 2ug alpha thrombin overnight under reducing conditions, with or without the 3CLPro inhibitor GC376 (1uM). C) In vitro cleavage of purified recombinant NOTCH1 fragment (aa2280-2550) with a N-terminal His-Tag. Reactions were done with 1uM of purified 3CLPro for 1hr. Diagram shows position of cleavage within the NOTCH1 fragment, with amino acid positions corresponding to the full length protein. Epitope regions showed for antibody with epitope C-terminal to the cleavage site. Full length size is ∼29kDa, with N and C-terminal fragments of 4kDa and 25kDa (respectively). D) Cellular cleavage of NOTCH1. Western blots show lysates of hIPSC cardiomyocytes expressing 3CLPro or catalytically inactive C145A variant for 48h. Cleavage site position within the intracellular fragment of NOTCH1 shown, as well as epitope for antibody used in western blot. For all statistics shown, * = p ≤ 0.05 , ** p ≤ 0.01, ***p ≤ 0.001, **** = p ≤ 0.00001

    Article Snippet: Recombinant proteins were purchased commercially: NOTCH1 (Origene, Cat# TP762041), CDH6 (ACROBiosystem, Cat# CA6-H5229), CDH20 (R&D, Cat# 5604-CA-050).

    Techniques: Western Blot, In Vitro, Recombinant, Purification, Incubation, Staining, Expressing, Variant Assay

    Materials

    Journal: Journal of visualized experiments : JoVE

    Article Title: Using microarrays to interrogate microenvironmental impact on cellular phenotypes in cancer.

    doi: 10.3791/58957

    Figure Lengend Snippet: Materials

    Article Snippet: Cadherin-20 (CDH20) , R & D Systems , 5604-CA , ECM.

    Techniques: Imaging, Inverted Microscopy, Microarray, Electron Microscopy

    The full list of ECM proteins and conditions that are used in the MEMA experiments. The uniprot ID, stock concentrations, and final working concentrations are provided. In some instances, the printed condition represents a protein complex or a combination of multiple proteins, which is indicated in the notes column.

    Journal: Journal of visualized experiments : JoVE

    Article Title: Using microarrays to interrogate microenvironmental impact on cellular phenotypes in cancer.

    doi: 10.3791/58957

    Figure Lengend Snippet: The full list of ECM proteins and conditions that are used in the MEMA experiments. The uniprot ID, stock concentrations, and final working concentrations are provided. In some instances, the printed condition represents a protein complex or a combination of multiple proteins, which is indicated in the notes column.

    Article Snippet: Cadherin-20 (CDH20) , R & D Systems , 5604-CA , ECM.

    Techniques: Concentration Assay

    Materials

    Journal: Journal of visualized experiments : JoVE

    Article Title: Using microarrays to interrogate microenvironmental impact on cellular phenotypes in cancer.

    doi: 10.3791/58957

    Figure Lengend Snippet: Materials

    Article Snippet: Cadherin-20 (CDH20) , R & D Systems , 5604-CA , ECM.

    Techniques: Imaging, Inverted Microscopy, Microarray, Electron Microscopy