Mouse Anti-HS2ST1 Recombinant Antibody (CBFYH-1975) (CBMAB-H2986-FY)

Basic Information
Formulations & Storage [For reference only, actual COA shall prevail!]
Target
Heparan sulfate proteoglycan biosynthetic process, enzymatic modification Source: GO_Central
Heparan sulfate proteoglycan biosynthetic process, polysaccharide chain biosynthetic process Source: GO_Central
An autosomal recessive syndrome characterized by developmental delay and/or intellectual disability, corpus callosum agenesis or hypoplasia, flexion contractures, brachydactyly of hands and feet with broad fingertips and toes, and dysmorphic features such as coarse face, upslanted palpebral fissures, broad nasal tip and wide mouth. Some patients manifest unilateral or bilateral renal agenesis.
Helical: 12-28
Lumenal: 29-356
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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
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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