Mouse Anti-FUCA1 Recombinant Antibody (CBYC-A959) (CBMAB-A4412-YC)

Basic Information
Formulations & Storage [For reference only, actual COA shall prevail!]
Target
Glycolipid catabolic process Source: BHF-UCL
Glycosaminoglycan catabolic process Source: UniProtKB
Glycoside catabolic process Source: UniProtKB
An autosomal recessive lysosomal storage disease characterized by accumulation of fucose-containing glycolipids and glycoproteins in various tissues. Clinical signs include facial dysmorphism, dysostosis multiplex, moderate hepatomegaly, severe intellectual deficit, deafness, and according to age, angiokeratomas.
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Please try the standard protocols which include: protocols, troubleshooting and guide.
Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme-Linked Immunospot (ELISpot)
Proteogenomics
Other Protocols
Antibody Pairs
FUCA1 Matched Antibody Pair (456) (CAT#: APMAB-456LY)
Related Products
Mouse Anti-FUCA1 Recombinant Antibody (CBXF-0955) (CAT#: CBMAB-F0992-CQ)
Mouse Anti-FUCA1 Recombinant Antibody (1D4) (CAT#: CBMAB-A4409-YC)
Mouse Anti-FUCA1 (AA 32-466) Recombinant Antibody (CBXF-3232) (CAT#: CBMAB-F3927-CQ)
Mouse Anti-FUCA1 Recombinant Antibody (CBYJT-1284) (CAT#: CBMAB-T0299-YJ)
FUCA1 Matched Antibody Pair (456) (CAT#: APMAB-456LY)
Rabbit Anti-FUCA1 Recombinant Antibody (CBXF-1101) (CAT#: CBMAB-F0993-CQ)
Custom Antibody Labeling
We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).
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