You Searched For: D(+)-Mannose

Catalog Number: (CAYM18890-500)

Supplier: Cayman Chemical

Description: D-Mannose-6-Phosphate (sodium salt hydrate) 1 * 500 mg

UOM: 1 * 500 mg

Catalog Number: (ABCAAB270683-100)

Supplier: Abcam

Description: PerCPCy5.5 Mouse monoclonal 15-2 to Mannose Receptor 1 * 100 Tests

UOM: 1 * 100 Tests

 This is a MarketSource item. Additional charges may apply

Catalog Number: (USBIC2548-96Y-100)

Supplier: US Biological

Description: CD206 MR, MANNOSE RECEPTOR C T MAB MO XH 1 * 100 G

UOM: 1 * 100 µG

Catalog Number: (ABCAAB270682-100)

Supplier: Abcam

Description: PECy7 Mouse monoclonal 15-2 to Mannose Receptor 1 * 100 Tests

UOM: 1 * 100 Tests

 This is a MarketSource item. Additional charges may apply

Catalog Number: (ABCAAB270647-100)

Supplier: Abcam

Description: FITC Mouse monoclonal 15-2 to Mannose Receptor 1 * 100 Tests

UOM: 1 * 100 Tests

 This is a MarketSource item. Additional charges may apply

Catalog Number: (PRSI30-230)

Supplier: ProSci Inc.

Description: LMAN2 plays a role as an intracellular lectin in the early secretory pathway. It interacts with N-acetyl-D-galactosamine and high-mannose type glycans and may also bind to O-linked glycans. It is involved in the transport and sorting of glycoproteins carrying high mannose-type glycans.

UOM: 1 * 50 µG

Catalog Number: (BOSSBS-13461R-A750)

Supplier: Bioss

Description: GMPPB is a 360 amino acid protein that belongs to the transferase hexapeptide repeat family and is involved in protein modification pathways. Functioning as a GDP-mannose pyrophosphorylase, GMPPB enzymatically catalyzes the conversion of mannose-1-phosphate and GTP to GDP-mannose and a free phosphate, a reaction that is involved in the production of N-linked oligosaccharides. Defects in the gene encoding GMPPB that cause errors in the glycosylation pathway may lead to congenital disorders of glycosylation (CDG). CDGs are multisystemic diseases that often involve both the central and peripheral nervous systems and are often characterized by endocrine and coagulation disorders. GMPPB is expressed as two isoforms due to alternative splicing events.

UOM: 1 * 100 µl

Catalog Number: (PRSI30-229)

Supplier: ProSci Inc.

Description: LMAN2 plays a role as an intracellular lectin in the early secretory pathway. It interacts with N-acetyl-D-galactosamine and high-mannose type glycans and may also bind to O-linked glycans. It is involved in the transport and sorting of glycoproteins carrying high mannose-type glycans.

UOM: 1 * 50 µG

Catalog Number: (BOSSBS-13461R-CY5)

Supplier: Bioss

Description: GMPPB is a 360 amino acid protein that belongs to the transferase hexapeptide repeat family and is involved in protein modification pathways. Functioning as a GDP-mannose pyrophosphorylase, GMPPB enzymatically catalyzes the conversion of mannose-1-phosphate and GTP to GDP-mannose and a free phosphate, a reaction that is involved in the production of N-linked oligosaccharides. Defects in the gene encoding GMPPB that cause errors in the glycosylation pathway may lead to congenital disorders of glycosylation (CDG). CDGs are multisystemic diseases that often involve both the central and peripheral nervous systems and are often characterized by endocrine and coagulation disorders. GMPPB is expressed as two isoforms due to alternative splicing events.

UOM: 1 * 100 µl

Catalog Number: (ABCAAB313671-10UL)

Supplier: Abcam

Description: Alexa Fluor 647 Rabbit monoclonal [EPR22489-7] to Mannose Receptor 1 * 10 l

UOM: 1 * 10 µl

 This is a MarketSource item. Additional charges may apply

Catalog Number: (ABCAAB254471-1)

Supplier: Abcam

Description: Rabbit monoclonal EPR22489-7 to Mannose Receptor - BSA and Azide free 1 * 1 mg

UOM: 1 * 1 mg

 This is a MarketSource item. Additional charges may apply

Catalog Number: (BOSSBS-13461R-CY7)

Supplier: Bioss

Description: GMPPB is a 360 amino acid protein that belongs to the transferase hexapeptide repeat family and is involved in protein modification pathways. Functioning as a GDP-mannose pyrophosphorylase, GMPPB enzymatically catalyzes the conversion of mannose-1-phosphate and GTP to GDP-mannose and a free phosphate, a reaction that is involved in the production of N-linked oligosaccharides. Defects in the gene encoding GMPPB that cause errors in the glycosylation pathway may lead to congenital disorders of glycosylation (CDG). CDGs are multisystemic diseases that often involve both the central and peripheral nervous systems and are often characterized by endocrine and coagulation disorders. GMPPB is expressed as two isoforms due to alternative splicing events.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-13461R-CY3)

Supplier: Bioss

Description: GMPPB is a 360 amino acid protein that belongs to the transferase hexapeptide repeat family and is involved in protein modification pathways. Functioning as a GDP-mannose pyrophosphorylase, GMPPB enzymatically catalyzes the conversion of mannose-1-phosphate and GTP to GDP-mannose and a free phosphate, a reaction that is involved in the production of N-linked oligosaccharides. Defects in the gene encoding GMPPB that cause errors in the glycosylation pathway may lead to congenital disorders of glycosylation (CDG). CDGs are multisystemic diseases that often involve both the central and peripheral nervous systems and are often characterized by endocrine and coagulation disorders. GMPPB is expressed as two isoforms due to alternative splicing events.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-13461R-A647)

Supplier: Bioss

Description: GMPPB is a 360 amino acid protein that belongs to the transferase hexapeptide repeat family and is involved in protein modification pathways. Functioning as a GDP-mannose pyrophosphorylase, GMPPB enzymatically catalyzes the conversion of mannose-1-phosphate and GTP to GDP-mannose and a free phosphate, a reaction that is involved in the production of N-linked oligosaccharides. Defects in the gene encoding GMPPB that cause errors in the glycosylation pathway may lead to congenital disorders of glycosylation (CDG). CDGs are multisystemic diseases that often involve both the central and peripheral nervous systems and are often characterized by endocrine and coagulation disorders. GMPPB is expressed as two isoforms due to alternative splicing events.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-13461R-A488)

Supplier: Bioss

Description: GMPPB is a 360 amino acid protein that belongs to the transferase hexapeptide repeat family and is involved in protein modification pathways. Functioning as a GDP-mannose pyrophosphorylase, GMPPB enzymatically catalyzes the conversion of mannose-1-phosphate and GTP to GDP-mannose and a free phosphate, a reaction that is involved in the production of N-linked oligosaccharides. Defects in the gene encoding GMPPB that cause errors in the glycosylation pathway may lead to congenital disorders of glycosylation (CDG). CDGs are multisystemic diseases that often involve both the central and peripheral nervous systems and are often characterized by endocrine and coagulation disorders. GMPPB is expressed as two isoforms due to alternative splicing events.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-13461R-A680)

Supplier: Bioss

Description: GMPPB is a 360 amino acid protein that belongs to the transferase hexapeptide repeat family and is involved in protein modification pathways. Functioning as a GDP-mannose pyrophosphorylase, GMPPB enzymatically catalyzes the conversion of mannose-1-phosphate and GTP to GDP-mannose and a free phosphate, a reaction that is involved in the production of N-linked oligosaccharides. Defects in the gene encoding GMPPB that cause errors in the glycosylation pathway may lead to congenital disorders of glycosylation (CDG). CDGs are multisystemic diseases that often involve both the central and peripheral nervous systems and are often characterized by endocrine and coagulation disorders. GMPPB is expressed as two isoforms due to alternative splicing events.

UOM: 1 * 100 µl