40 Results for "

Arg1

" in MedChemExpress (MCE) Product Catalog:
Products (40)

40 Results for "Arg1" in MCE Product Catalog:

Cat. No.: HY-P7541
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Arg1; Type I Arginase; Arginase 1; Arginase, Liver; Arginase-1; Arginase; Liver-Type Arginase
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P7602
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Arg1; Type I Arginase; Arginase 1; Arginase, Liver; Arginase-1; Arginase; Liver-Type Arginase
Species:  
Human
Source:  
HEK293
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Cat. No.: HY-P991870

Target:  

Arginase

Research Areas:  

Cancer

Anti-Arginase-1 Antibody is an antibody against human Arginase-1/ARG1. Recommend Isotype Controls:?Human IgG1 kappa, Isotype Control (HY-P99001).
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Cat. No.: HY-P86409
Synonyms: Arginase-1, Liver-type Arginase, Type I Arginase, Arg1

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, IP, ELISA

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-RS14543
Research Areas:  

Others

TINAGL1 Human Pre-designed siRNA Set A contains three designed siRNAs for TINAGL1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-163426S
Research Areas:  

Others

AFFGHYLYEVAR-(Arg- 13C6, 15N4) is 13C and 15N labeled AFFGHYLYEVAR-(Arg) .
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Cat. No.: HY-P6423S
Research Areas:  

Others

CLAVYQAGA-Arg( 13C6, 15N4) TFA is a peptide containing 13C6 and 15N4 labeled Arg .
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Cat. No.: HY-100742AR
CAS No.: 2003234-63-5
Research Areas:  

Cancer

(R)-GNE-140 (Standard) is the analytical standard of (R)-GNE-140 (HY-100742A). This product is intended for research and analytical applications. (R)-GNE-140 is a potent inhibitor of lactate dehydrogenase (LDH) A, B and C, with IC50 values of 3, 5 and 5 nM against LDHA, LDHB, LDHC, respectively. (R)-GNE-140 blocks the conversion of pyruvate to lactate, reduces lactate production and histone lysine lactylation, and inhibits glycolysis. (R)-GNE-140 attenuates cardiac hypertrophy, alleviates PM2.5-induced pulmonary inflammation and fibrosis, blocks MRSA-induced Arg1 expression. (R)-GNE-140 is applicable to research related to pathological cardiac hypertrophy, pulmonary fibrosis, MRSA infection and pancreatic cancer [1] .
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Cat. No.: HY-N20682
CAS No.: 2866266-56-8
1-Hydroxy-4αH-1,10-secoeudesma-5(6),10(14),11(13)-trien-12,8β-olide is a neuroprotective agent. 1-Hydroxy-4αH-1,10-secoeudesma-5(6),10(14),11(13)-trien-12,8β-olide reduces the protein expression levels of iNOS and COX-2, blocks the DNA-binding activity of NF-κB, and inhibits nitric oxide production. 1-Hydroxy-4αH-1,10-secoeudesma-5(6),10(14),11(13)-trien-12,8β-olide promotes the polarization of microglia to the M2 phenotype by inducing the production of Arg-1, and alleviates cell damage induced by H2O2 and 6-Hydroxydopamine (HY-B1081) [1].
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Cat. No.: HY-P71369
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: TINAGL1; Lipocalin 7; Prev. LCN7; OLRG-2; TINAGRP; Tubulointerstitial Nephritis Antigen-Like 1, Isoform CRA_a; P3ECSL; Oxidized LDL-Responsive Gene 2 Protein; LIECG3; Oxidized-LDL Responsive Gene 2; Arg1; Androgen Regulated Gene 1; Tubulointerstitial Neph
Species:  
Human
Source:  
HEK293
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Cat. No.: HY-P11882
CAS No.: 947545-69-9
Target:  

Fc Receptor (FcR)

Research Areas:  

Inflammation/Immunology

SYN1436 is a selective human neonatal Fc receptor (hFcRn) antagonist with an IC50 of 2.4 nM. SYN1436 binds to hFcRn and inhibits hFcRn-hIgG interaction. SYN1436 can be used for the research of autoimmune diseases [1].
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Cat. No.: HY-187035
CAS No.: 868066-26-6
Target:  

CDK STAT

Research Areas:  

Cancer

SNX631 is an orally active and selective CDK8/CDK19 inhibitor. SNX631 reduces the phosphorylation of STAT1/STAT3 S727, and upregulates miR-21-5p, miR-21-3p and miR-221 in cancer cells. SNX631 transcription-independently inhibits meiotic resumption in mouse oocytes, blocks nuclear envelope breakdown, first polar body extrusion and mitochondrial expansion and aggregation, with no cytotoxicity. SNX631, in combination with Lapatinib (HY-50898) or Trastuzumab (HY-P9907), synergistically inhibits cancer cell growth, upregulates the tumor suppressor BTG2, prevents Lapatinib-induced upregulation of oncogenic miRNAs, overcomes drug resistance, reduces the infiltration of αSMA+ stromal fibroblasts and ARG1+ M2 macrophages, and exhibits favorable biosafety. SNX631 can be used in studies related to HER2-positive breast cancer and cancer [1] .
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Cat. No.: HY-P80019

Host:  

Rabbit

Application:  

WB, IHC-P

Reactivity:  

Human

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Cat. No.: HY-RS18727
Research Areas:  

Others

Tinagl1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Tinagl1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P6421S
LGPLVEQG-Arg( 13C6, 15N4) TFA is a peptide containing 13C6 and 15N4 labeled Arg .
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Cat. No.: HY-P6422S
Research Areas:  

Others

LAVYQAGA-Arg( 13C6, 15N4) TFA is a peptide containing 13C6 and 15N4 labeled Arg .
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Cat. No.: HY-P6424S
Research Areas:  

Others

LGADMEDVCG-Arg( 13C6, 15N4) TFA is a peptide containing 13C6 and 15N4 labeled Arg .
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Cat. No.: HY-P6425S
Research Areas:  

Others

LCADMEDV-Arg( 13C6, 15N4) TFA is a peptide containing 13C6 and 15N4 labeled Arg .
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Cat. No.: HY-182719
CAS No.: 2374807-41-5
Target:  

Arginase

Research Areas:  

Cancer

AZD0011, a prodrug of AZD0011-PL (HY-182718), is an orally active arginase 1 inhibitor with an IC50 of 328 nM. AZD0011 undergoes in vivo hydrolysis to release an arginase inhibitor payload, inhibiting arginine hydrolysis, increases arginine levels in plasma and the tumor microenvironment. AZD0011 restores innate immune function and inhibits tumor growth. AZD0011 can be used for the research of cancer, such as fibrosarcoma [1].
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Cat. No.: HY-184203
Target:  

HDAC

Research Areas:  

Cancer

SM-06-09 is a potent, highly selective, orally active tetrazolone-based HDAC6 inhibitor with an IC50 value of 0.49 nM. SM-06-09 promotes tumor-associated macrophage (TAM) polarization toward an antitumor M1-like phenotype and enhances macrophage phagocytosis, antigen presentation, and T-cell activation. SM-06-09 remodels the tumor immune microenvironment, exhibits antitumor activity in melanoma models, and enhances the efficacy of anti-PD-1 immune checkpoint blockade [1].
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