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ARSA Antibody (C-term)

Mouse Monoclonal Antibody (Mab)

     
  • WB - ARSA Antibody (C-term) AM2083b
    ARSA Antibody (C-term) (Cat. #AM2083b) western blot analysis in Jurkat cell line lysates (35μg/lane).This demonstrates the ARSA antibody detected the ARSA protein (arrow).
    detail
  • SPECIFICATION
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Product Information
Application
  • 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
  • E=ELISA
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
WB, E
Primary Accession P15289
Other Accession NP_000478.2
Reactivity Human
Host Mouse
Clonality Monoclonal
Isotype IgG2a
Clone/Animal 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~~1:500~1000
Format Purified monoclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein G column, followed by dialysis against PBS.
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) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name ARSA
Function Hydrolyzes cerebroside sulfate.
Cellular Location Endoplasmic reticulum. Lysosome
Research Areas
Citations (0)
citation

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Background

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.

References

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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$ 182.50
$ 70.00
Cat# AM2083b
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