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Goat Anti-Arylsulfatase A Antibody

Peptide-affinity purified goat antibody

     
  • WB - Goat Anti-Arylsulfatase A Antibody AF1113a
    AF1113a (0.5 µg/ml) staining of Mouse Testis lysate (35 µg protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
    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, 410, 11883 (mouse), 315222 (rat)
Reactivity Mouse
Predicted Human, Rat
Host Goat
Clonality Polyclonal
Concentration 100ug/200ul
Isotype IgG
Calculated MW 53588 Da
Additional Information
Gene ID 410
Other Names Arylsulfatase A, ASA, 3.1.6.8, Cerebroside-sulfatase, Arylsulfatase A component B, Arylsulfatase A component C, ARSA
Format 0.5 mg IgG/ml in Tris saline (20mM Tris pH7.3, 150mM NaCl), 0.02% sodium azide, with 0.5% bovine serum albumin
StorageMaintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
PrecautionsGoat Anti-Arylsulfatase A Antibody 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. Multiple alternatively spliced transcript variants, one of which encodes a distinct protein, have been described for this gene.

References

Characterization of new arylsulfatase A gene mutations reinforces genotype-phenotype correlation in metachromatic leukodystrophy. Cesani M, et al. Hum Mutat, 2009 Oct. PMID 19606494.
Characterization of the arylsulfatase I (ARSI) gene preferentially expressed in the human retinal pigment epithelium cell line ARPE-19. Oshikawa M, et al. Mol Vis, 2009. PMID 19262745.
Saposin B-dependent reconstitution of arylsulfatase A activity in vitro and in cell culture models of metachromatic leukodystrophy. Matzner U, et al. J Biol Chem, 2009 Apr 3. PMID 19224915.
Chromosomal deletion unmasking a recessive disease: 22q13 deletion syndrome and metachromatic leukodystrophy. Bisgaard AM, et al. Clin Genet, 2009 Feb. PMID 19054018.
Molecular and clinical consequences of novel mutations in the arylsulfatase A gene. 艁ugowska A, et al. Clin Genet, 2009 Jan. PMID 19021637.

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$ 341.00
Cat# AF1113a
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Availability: 7-10 days
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