9 Results for "

UBE2M

" in MedChemExpress (MCE) Product Catalog:
Products (9)

9 Results for "UBE2M" in MCE Product Catalog:

4
4 Cited Publications
Cat. No.: HY-111505
CAS No.: 2089293-61-6
Purity:  99.65%
Research Areas:  

Cancer

NAcM-OPT is an orally bioavailable cullin neddylation 1 (DCN1) inhibitor, which potently inhibits the DCN1-UBE2M interaction .
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Cat. No.: HY-RS15355
Research Areas:  

Others

UBE2M Human Pre-designed siRNA Set A contains three designed siRNAs for UBE2M gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS19492
Research Areas:  

Others

Ube2m Mouse Pre-designed siRNA Set A contains three designed siRNAs for Ube2m gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS25986
Research Areas:  

Others

Ube2m Rat Pre-designed siRNA Set A contains three designed siRNAs for Ube2m gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P71406
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: UBE2M; Ubiquitin Conjugating Enzyme E2 M; UBC12; NEDD8-Conjugating Enzyme Ubc12; NEDD8 Carrier Protein; HUbc12; Ubiquitin-Conjugating Enzyme E2M (UBC12 Homolog, Yeast); Ubiquitin-Conjugating Enzyme E2 M; Ubiquitin-Conjugating Enzyme E2M (Homologous To Yea
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-111505R
CAS No.: 2089293-61-6
NAcM-OPT (Standard) is the analytical standard of NAcM-OPT (HY-111505). This product is intended for research and analytical applications. NAcM-OPT is an orally bioavailable cullin neddylation 1 (DCN1) inhibitor, which potently inhibits the DCN1-UBE2M interaction .
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Cat. No.: HY-P88113
Synonyms: hUbc12; UBC-RS2; UBC12

Host:  

Mouse

Application:  

WB, ICC/IF

Reactivity:  

Human, Dog, Monkey, Mouse, Rat

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Cat. No.: HY-P88113A
Synonyms: hUbc12; UBC-RS2; UBC12

Host:  

Mouse

Application:  

WB, ICC/IF

Reactivity:  

Human, Dog, Monkey, Mouse, Rat

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Cat. No.: HY-189074
Research Areas:  

Cancer

JN210 is a dual inhibitor of DCN1 and HDAC, with an IC50 of 94.26 nM against human DCN1. JN210 disrupts the UBE2M-DCN1 protein-protein interaction, blocks the neddylation modification of cullin-RING ligases, inhibits HDAC activity and induces histone hyperacetylation. JN210 impairs DNA damage repair function, induces cell apoptosis, exerts cytotoxicity and inhibits tumor growth. JN210 can be used for the research of non-small cell lung cancer .
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