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>   home   >   Products   >   Primary Antibodies   >   Neuroscience   >   ARSA Antibody (C-term) (Ascites)   

ARSA Antibody (C-term) (Ascites)

Mouse Monoclonal Antibody (Mab)

  • WB - ARSA Antibody (C-term) (Ascites) AM2083a
    ARSA Antibody (C-term) (Cat. #AM2083a) western blot analysis in Jurkat cell line lysates (35μg/lane).This demonstrates the ARSA antibody detected the ARSA protein (arrow).
Product Information
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Primary Accession P15289
Other Accession NP_000478.2
Reactivity Human
Host Mouse
Clonality Monoclonal
Isotype IgG2a
Clone Names 498CT24.1.2
Calculated MW 53588 Da
Antigen Region 408-439 aa
Additional Information
Gene ID 410
Other Names Arylsulfatase A, ASA, Cerebroside-sulfatase, Arylsulfatase A component B, Arylsulfatase A component C, ARSA
Target/Specificity This ARSA antibody is generated from mice immunized with a KLH conjugated synthetic peptide between 408-439 amino acids from the C-terminal region of human ARSA.
Dilution WB~~1:500~4000
Format Mouse monoclonal antibody supplied in crude ascites with 0.09% (W/V) sodium azide.
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
PrecautionsARSA Antibody (C-term) (Ascites) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Function Hydrolyzes cerebroside sulfate.
Cellular Location Lysosome.
Research Areas
Citations (0)

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The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy (MLD), a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Alternatively spliced transcript variants have been described for this gene.


Cesani, M., et al. Hum. Mutat. 30 (10), E936-E945 (2009) :
Matzner, U., et al. J. Biol. Chem. 284(14):9372-9381(2009)
Bisgaard, A.M., et al. Clin. Genet. 75(2):175-179(2009)
Lugowska, A., et al. Clin. Genet. 75(1):57-64(2009)
Oshikawa, M., et al. Mol. Vis. 15, 482-494 (2009) :

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$ 295.00
Cat# AM2083a
(40 western blots)
Availability: In Stock
Bulk Size
Seasonal Special on Bulk Order
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