25 Results for "

NOG

" in MedChemExpress (MCE) Product Catalog:
Products (25)

25 Results for "NOG" in MCE Product Catalog:

Cat. No.: HY-P85580
Synonyms: NOG; NOGG_HUMAN; NOGgin; SYM 1; SYM1; Symphalangism 1; proximal; Synostoses; multiple; syndrome 1; SYNS 1; SYNS1.

Host:  

Mouse

Application:  

WB, ICC/IF

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Cat. No.: HY-P82444
Synonyms: CRFG; GTP binding protein 4; Gtpbp4; NGB; NOG1

Host:  

Rabbit

Application:  

WB, IHC-P, IP, FC

Reactivity:  

Human

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Cat. No.: HY-187562
Target:  

Wee1 CDK

Research Areas:  

Cancer

PKMYT1-IN-15 is an orally active PKMYT1 inhibitor with an IC50 of 6.02 nM. PKMYT1-IN-15 inhibits the phosphorylation of CDK1 at Thr14. As an antiproliferative agent, DNA damage inducer and antitumor agent, PKMYT1-IN-15 triggers replication-associated DNA damage and cell death in CCNE1-amplified cancer cells, and suppresses tumor growth in the OVCAR3 xenograft model. PKMYT1-IN-15 can be used for the research of CCNE1-amplified cancers (e.g., ovarian cancer, breast cancer) .
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Cat. No.: HY-P992381

Target:  

Drug Derivative

Research Areas:  

Cancer

IBI352g4a is a humanized IgG1 monoclonal antibody targeting PVRIG (Kd = 0.53 nM) and acts as a PVRIG/PVRL2 inhibitor. The anti-tumor effect of IBI352g4a depends on the binding of its Fc region to FcγR. IBI352g4a binds to the extracellular domains of human and cynomolgus monkey PVRIG, and blocks the PVRIG-PVRL2 interaction. IBI352g4a induces NK cell activation, promotes their degranulation and tumor killing. IBI352g4a can be used in the research of gastric cancer .
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Cat. No.: HY-184500
CAS No.: 2923223-81-6
Research Areas:  

Cancer

TNG917 is a potent, selective EHMT1/2 inhibitor with oral activity. TNG917 reduces H3K9me2-mediated transcriptional repression, restores interferon-stimulated gene expression, promotes the secretion of T-cell chemokines such as CXCL10, and converts immunologically cold tumors into T-cell inflamed tumors. TNG917 is applicable to studies on immunologically cold tumors, colorectal cancer, anti-tumor immunity, interferon signaling pathways and epigenetic immune escape .
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