16 Results for "

UCHL5

" in MedChemExpress (MCE) Product Catalog:
Products (16)

16 Results for "UCHL5" in MCE Product Catalog:

  • Recombinant Proteins Recommended:
13
13 Cited Publications
Cat. No.: HY-13989
CAS No.: 1009817-63-3
Purity:  98.57%
Synonyms: NSC 687852
Research Areas:  

Cancer

b-AP15 is a specific inhibitor of the deubiquitinating enzymes UCHL5 and Usp14.
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Cat. No.: HY-149230
CAS No.: 2931509-15-6
Purity:  99.35%
Target:  

Deubiquitinase

Research Areas:  

Cancer

USP28-IN-4 is a USP28 inhibitor (IC50=0.04 μM) with high selectivity over USP2, USP7, USP8, USP9x, UCHL3 and UCHL5. USP28-IN-4 shows cytotoxicity against cancer cells, down-regulates the cellular level of c-Myc through ubiquitin-proteasome system. USP28-IN-4 also decreases the ankyrase-1/2 level in vitro. USP28-IN-4 enhance the sensitivity of colorectal cancer cells to Regorafenib (HY-10331) .
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Cat. No.: HY-RS15402
Research Areas:  

Others

UCHL5 Human Pre-designed siRNA Set A contains three designed siRNAs for UCHL5 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS18192
Research Areas:  

Others

Uchl5 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Uchl5 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS24666
Research Areas:  

Others

Uchl5 Rat Pre-designed siRNA Set A contains three designed siRNAs for Uchl5 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-149229
CAS No.: 2931509-14-5
Purity:  98.26%
Target:  

Deubiquitinase

Research Areas:  

Cancer

USP28-IN-3 is a USP28 inhibitor (IC50=0.1 μM) with high selectivity over USP2, USP7, USP8, USP9x, UCHL3 and UCHL5. USP28-IN-3 shows cytotoxicity against cancer cells, down-regulates the cellular level of c-Myc through ubiquitin-proteasome system. USP28-IN-3 also decreases the ankyrase-1/2 level in vitro. USP28-IN-3 enhance the sensitivity of colorectal cancer cells to Regorafenib (HY-10331) .
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Cat. No.: HY-149228
CAS No.: 2931509-11-2
Target:  

Deubiquitinase

Research Areas:  

Cancer

USP28-IN-2 is a USP28 inhibitor (IC50=0.3 μM) with high selectivity over USP2, USP7, USP8, USP9x, UCHL3 and UCHL5. USP28-IN-2 shows cytotoxicity against cancer cells, down-regulates the cellular level of c-Myc through ubiquitin-proteasome system. USP28-IN-2 also decreases the ankyrase-1/2 level in vitro. USP28-IN-2 enhance the sensitivity of colorectal cancer cells to Regorafenib (HY-10331) .
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Cat. No.: HY-15432
CAS No.: 330450-45-8
Synonyms: (E/Z)-b-AP15
Target:  

Deubiquitinase

Research Areas:  

Cancer

(E/Z)-NSC-687852 is a isomer of NSC-687852 (HY-13989). NSC687852 (b-AP15) is a specific inhibitor of the deubiquitinating enzymes UCHL5 and Usp14 .
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Cat. No.: HY-164689
CAS No.: 18897-36-4
Target:  

Proteasome

Research Areas:  

Cancer

Cadmium pyrithione is a metal compound that inhibits protein deubiquitinase activity. Cadmium pyrithione treatment results in significant accumulation of ubiquitinated proteins in cancer cells and primary leukemia cells. Cadmium pyrithione strongly inhibits the activity of proteasome deubiquitinase (such as USP14 and UCHL5), but has a smaller inhibitory effect on 20S proteasome activity. The anticancer activity of Cadmium pyrithione is associated with the induction of apoptosis through caspase activation. Furthermore, Cadmium pyrithione inhibition inhibited proteasome function and suppressed tumor growth in animal xenograft models .
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Cat. No.: HY-P701406
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: UCHL5; Ubiquitin C‑Terminal Hydrolase L5; UCH37; CGI‑70; INO80R; Ubiquitin Carboxyl‑Terminal Hydrolase Isozyme L5; Ubiquitin Carboxyl‑Terminal Hydrolase L5; Ubiquitin C‑Terminal Hydrolase UCH37; Ubiquitin Thioesterase L5; INO80 Complex Subunit R; UCH‑L5;
Species:  
Source:  
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Cat. No.: HY-P82594
Synonyms: UCH37; CGI-70; INO80R; UCH-L5

Host:  

Rabbit

Application:  

WB, ICC/IF, IP

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-D1236
CAS No.: 16090-02-1
Fluorescent brightener 71 (FB71) is an inhibitor targeting deubiquitinases UCHL5 and USP14, as well as a CD40 ligand. Fluorescent brightener 71 blocks enzymatic activity, induces apoptosis, inhibits cell growth and triggers reactive oxygen species production. Meanwhile, Fluorescent brightener 71 upregulates the expression of oxidative stress-related genes gpx-4 and sod-4, and reversibly increases the protein levels of UCHL5 and USP14 through a feedback response. Fluorescent brightener 71 inhibits the growth, movement and reproductive capacity of Caenorhabditis elegans, and also exhibits concentration-dependent toxic effects. Fluorescent brightener 71 can be applied to scientific research in related fields such as breast cancer .
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Cat. No.: HY-P82594A
Synonyms: UCH37; CGI-70; INO80R; UCH-L5

Host:  

Rabbit

Application:  

WB, ICC/IF, IP

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P87575

Host:  

Rabbit

Application:  

IHC-P, IHC-F, IF-Tissue, IP

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Cat. No.: HY-P82598
Synonyms: UIP1; UCHL5IP

Host:  

Rabbit

Application:  

WB

Reactivity:  

Human

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Cat. No.: HY-P82598A
Synonyms: UIP1; UCHL5IP

Host:  

Rabbit

Application:  

WB

Reactivity:  

Human

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