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GALNS antibody (AA 20-269)
This Rabbit Polyclonal antibody specifically detects GALNS in WB, IHC and IF. It exhibits reactivity toward Human.
Quick Overview for GALNS antibody (AA 20-269) (ABIN1886170)
Target
See all GALNS Antibodies
GALNS
(Galactosamine (N-Acetyl)-6-Sulfate Sulfatase (GALNS))
Reactivity
All reactivities for GALNS antibodies
Human
Host
All hosts for GALNS antibodies
Rabbit
Clonality
All clonalities for GALNS antibodies
Polyclonal
Conjugate
All conjugates for GALNS antibodies
This GALNS antibody is un-conjugated
Application
All applications for GALNS antibodies
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
Product Details anti-GALNS Antibody
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Binding Specificity
All epitopes for GALNS antibodies
AA 20-269
Purification
Purified by antigen-affinity chromatography.
Immunogen
Recombinant protein fragment contain a sequence corresponding to a region within amino acids 20 and 269 of GALNS
Alternatives
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Application Details
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Application Notes
Suggested dilutions: Western blotting: 1.500-1.3000 Immunohistochemistry: 1.100-1.500 Immunofluorescence: 1.100-1.200
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
Preservative
Thimerosal (Merthiolate)
Precaution of Use
Biohazard Informations: This product contains thimerosal which is hazardous.
Storage
4 °C/-20 °C
Storage Comment
Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
Target Details for GALNS
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Target
GALNS
(Galactosamine (N-Acetyl)-6-Sulfate Sulfatase (GALNS))
Alternative Name
GALNS
Background
This gene encodes N-acetylgalactosamine-6-sulfatase which is a lysosomal exohydrolase required for the degradation of the glycosaminoglycans, keratan sulfate, and chondroitin 6-sulfate.Sequence alterations including point, missense and nonsense mutations, as well as those that affect splicing, result in a deficiency of this enzyme.Deficiencies of this enzyme lead to Morquio A syndrome, a lysosomal storage disorder.[provided by RefSeq]
Molecular Weight
58 kDa
Gene ID
2588
NCBI Accession
NP_000503 , NM_000512
Pathways
Glycosaminoglycan Metabolic Process
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