You Searched For: D-(+)-Mannose

Catalog Number: (76708-590)

Supplier: AFG BIOSCIENCE LLC

Description: Mouse Macrophage Mannose Receptor 1(MRC1) ELISA Kit

Catalog Number: (76712-624)

Supplier: AFG BIOSCIENCE LLC

Description: Human C Type Mannose Receptor 2 (MRC2) ELISA Kit

Catalog Number: (10298-514)

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.

Catalog Number: (103222-336)

Supplier: Novus Biologicals

Description: Mannose Receptor Antibody, Polyclonal, Host: Goat, Species reactivity: Mouse, Isotype: IgG, Immunogen: Mouse myeloma cell line NS0-derived recombinant mouse MMR, Synonym: CLEC13Dmacrophage mannose receptor 1, CD206, CLEC13D, Application: WB, Size: 50UG

Supplier: Ambeed

Description: (2R,3R,4S,5S)-2,3,4,5-Tetrahydroxyhexanal, Purity: 97% (contains less than 9-12%H2O), CAS Number: 3615-41-6, Appearance: Solid, Storage: Sealed in dry, 2-8C, Size: 25G

Catalog Number: (89322-436)

Supplier: Genetex

Description: Canavalia ensiformis lectin against alpha-linked mannose and glucose (Biotin) Pkg Size: 1 mg

Catalog Number: (10298-382)

Supplier: Bioss

Description: GMD is a 372 amino acid protein that utilizes NADP as a cofactor to catalyze the conversion of GDP-mannose to GDP-4-keto-6-deoxymannose. GMD mutations are involved in resistance to TRAIL (tumor necrosis factor-related apoptosis-inducing ligand)-induced apoptosis. The gene encoding GMD maps to human chromosome 6, which contains 170 million base pairs and comprises nearly 6% of the human genome. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer, suggesting the presence of a cancer susceptibility locus. Additionally, Porphyria cutanea tarda, Parkinson's disease, Stickler syndrome and a susceptibility to bipolar disorder are all associated with genes that map to chromosome 6.

Catalog Number: (10209-102)

Supplier: Boster Biological Technology

Description: Rabbit IgG polyclonal antibody for Cation-independent mannose-6-phosphate receptor(IGF2R) detection. Tested with WB, IHC-P, ICC in Human;Mouse;Rat.

Catalog Number: (10298-510)

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.

Catalog Number: (77440-352)

Supplier: Bioss

Description: The protein encoded by this gene catalyzes the isomerization of mannose 6-phosphate to mannose 1-phosphate, which is a precursor to GDP-mannose necessary for the synthesis of dolichol-P-oligosaccharides. Mutations in this gene have been shown to cause defects in glycoprotein biosynthesis, which manifests as carbohydrate-deficient glycoprotein syndrome type I. (provided by RefSeq, Jul 2008).

Catalog Number: (77230-212)

Supplier: ANTIBODIES.COM LLC

Description: Rabbit monoclonal [ARC0538] antibody to Mannose Receptor for WB with samples derived from Human and Mouse.

Supplier: AFG BIOSCIENCE LLC

Description: N-azidoacetylmannosamine 95%

Catalog Number: (89280-916)

Supplier: Genetex

Description: Rat monoclonal antibody [MR5D3] to Mannose Receptor

Catalog Number: (10298-494)

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.

Catalog Number: (10298-512)

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.

Catalog Number: (10298-508)

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.