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β-N-Acetyl-D-hexosaminidase-IN-1

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Biochemical Assay Reagents (1) Glycosidase (2) Reference Standards (1)
By Research Areas:	Metabolic Disease (3)

Inhibitors & Agonists

Biochemical Assay Reagents

Recombinant Proteins

Antibodies

Art. -Nr.	Produktname	Target	Forschungsgebiete	Chemical Structure

HY-W011183

4-Nitrophenyl-N-acetyl-β-D-glucosaminide 1 Publications Verification	Biochemical Assay Reagents	Metabolic Disease
4-Nitrophenyl-N-acetyl-β-D-glucosaminide, an artificial substrate of N-acetyl-beta-D-hexosaminidase (NAGase), can be used in rapid and accurate rate assay for N-acetyl-beta-D-hexosaminidase. 4-Nitrophenyl-N-acetyl-β-D-glucosaminide is highly soluble and stable. 4-Nitrophenyl-N-acetyl-β-D-glucosaminide can be used for the study of renal tubular injury .

HY-104050

M-31850 2 Publications Verification	Glycosidase	Metabolic Disease
M-31850 is a potent, selective and competitive *β-hexosaminidase* (Hex) inhibitor with IC₅₀s of 6.0 μM and 3.1 μM for human HexA and human HexB*, respectively. M-31850 also competitively inhibits β-N-acetyl-D-hexosaminidase* OfHex2 with a K_i of 2.5 μM .

HY-139733

*β-N-Acetyl-D-hexosaminidase-IN-1*	Others	Others
β-N-Acetyl-D-hexosaminidase-IN-1 is a novel *β-N-acetyl-d-hexosaminidase* inhibitor with a K_i value of 3.72 μM.

HY-104050R

M-31850 (Standard)	Glycosidase Reference Standards	Metabolic Disease
M-31850 (Standard) is the analytical standard of M-31850 (HY-104050). This product is intended for research and analytical applications. M-31850 is a potent, selective and competitive β-hexosaminidase (Hex) inhibitor with IC₅₀s of 6.0 μM and 3.1 μM for human HexA and human HexB, respectively. M-31850 also competitively inhibits β-N-acetyl-D-hexosaminidase OfHex2 with a K_i of 2.5 μM .

Art. -Nr.	Produktname	Type

HY-W011183

4-Nitrophenyl-N-acetyl-β-D-glucosaminide 1 Publications Verification	Biochemical Assay Reagents
4-Nitrophenyl-N-acetyl-β-D-glucosaminide, an artificial substrate of N-acetyl-beta-D-hexosaminidase (NAGase), can be used in rapid and accurate rate assay for N-acetyl-beta-D-hexosaminidase. 4-Nitrophenyl-N-acetyl-β-D-glucosaminide is highly soluble and stable. 4-Nitrophenyl-N-acetyl-β-D-glucosaminide can be used for the study of renal tubular injury .

Art. -Nr.	Compare	Produktname	Species	Source	Image

HY-P79242

	O-GlcNAcase/OGA Protein, B. thetaiotaomicron (His) O-GlcNAcase BT_4395; Beta-N-Acetylglucosaminidase; Beta-N-Acetylhexosaminidase; Beta-hexosaminidase; hexosaminidase B; N-Acetyl-beta-glucosaminidase	Others	E. coli
	O-GlcNAcase (OGA) is an enzyme responsible for the hydrolysis of glycosidic bonds in O-GlcNA acylated proteins. It exhibits its enzymatic activity in vitro by efficiently utilizing substrates such as p-nitrophenyl-β-GlcNAc and 4-methylumbelliferone-GlcNAc. O-GlcNAcase/OGA Protein, B. thetaiotaomicron (His) is the recombinant O-GlcNAcase/OGA protein, expressed by E. coli , with N-6*His labeled tag.

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HY-P86899

	HEXB Antibody (YA6592) Beta hexosaminidase beta chain antibody; Beta hexosaminidase subunit beta antibody; Beta N Acetylhexosaminidase antibody; Beta-hexosaminidase subunit beta chain A antibody; Beta-N-Acetylhexosaminidase subunit beta antibody; Cervical cancer proto oncogene 7 protein antibody; Cervical cancer proto-oncogene 7 protein antibody; ENC 1AS antibody; Epididymis luminal protein 248 antibody; HCC 7 antibody; Beta hexosaminidase beta chain antibody; Beta hexosaminidase subunit beta antibody; Beta N Acetylhexosaminidase antibody; Beta-hexosaminidase subunit beta chain A antibody; Beta-N-Acetylhexosaminidase subunit beta antibody; Cervical cancer proto oncogene 7 protein antibody; Cervical cancer proto-oncogene 7 protein antibody; ENC 1AS antibody; Epididymis luminal protein 248 antibody; HCC 7 antibody; HCC-7 antibody; HCC7 antibody; HEL 248 antibody; HEX B antibody; Hexb antibody; HEXB_HUMAN antibody; hexosaminidase B (beta polypeptide) antibody; hexosaminidase B antibody; hexosaminidase subunit B antibody; hexosaminidaseB antibody; N Acetyl beta glucosaminidase antibody; N-Acetyl-beta-glucosaminidase subunit beta antibody;	WB, IHC-P, ICC/IF, FC, IF-Tissue	Human
	HEXB Antibody (YA6592) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to HEXB.

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BODIPY 493/503 purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Feb 1;16(1):1241. [Abstract]

MedchemExpress Validation 01

Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature. Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature. Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.

BODIPY 493/503 purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Feb 1;16(1):1241. [Abstract]

MedchemExpress Validation 01

MedchemExpress Validation 03

Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred

MedchemExpress Validation 04

MedchemExpress Validation

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