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Goat Anti-SUMF1 Antibody

Peptide-affinity purified goat antibody

  • WB - Goat Anti-SUMF1 Antibody AF2196a
    AF2196a (1 µg/ml) staining of Mouse Pancreas lysate (35 µg protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
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 Q8NBK3
Other Accession NP_877437, 285362, 58911 (mouse), 362409 (rat)
Reactivity Human, Mouse
Predicted Rat, Dog, Cow
Host Goat
Clonality Polyclonal
Concentration 100ug/200ul
Isotype IgG
Calculated MW 40556 Da
Additional Information
Gene ID 285362
Other Names Sulfatase-modifying factor 1, 1.8.99.-, C-alpha-formylglycine-generating enzyme 1, SUMF1, FGE
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-SUMF1 Antibody is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name SUMF1
Synonyms FGE
Function Using molecular oxygen and an unidentified reducing agent, oxidizes a cysteine residue in the substrate sulfatase to an active site 3-oxoalanine residue, which is also called C(alpha)-formylglycine. Known substrates include GALNS, ARSA, STS and ARSE.
Cellular Location Endoplasmic reticulum lumen
Tissue Location Ubiquitous. Highly expressed in kidney, pancreas and liver. Detected at lower levels in leukocytes, lung, placenta, small intestine, skeletal muscle and heart
Research Areas
Citations (0)

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This gene encodes an enzyme that catalyzes the hydrolysis of sulfate esters by oxidizing a cysteine residue in the substrate sulfatase to an active site 3-oxoalanine residue, which is also known as C-alpha-formylglycine. Mutations in this gene cause multiple sulfatase deficiency, a lysosomal storage disorder. Alternative splicing results in multiple transcript variants.


Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis. Baranzini SE, et al. Brain, 2010 Sep. PMID 20802204.
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.
Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families. Hara K, et al. Neurology, 2008 Aug 19. PMID 18579805.
Multiple sulfatase deficiency in a Turkish family resulting from a novel mutation. Yi? U, et al. Brain Dev, 2008 May. PMID 18509892.
Multistep, sequential control of the trafficking and function of the multiple sulfatase deficiency gene product, SUMF1 by PDI, ERGIC-53 and ERp44. Fraldi A, et al. Hum Mol Genet, 2008 Sep 1. PMID 18508857.

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$ 325.00
Cat# AF2196a
(40 western blots)
Availability: 7-10 days
Bulk Size
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