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ASPA antibody (AA 39-270)
ASPA
Reactivity: Human
WB, IHC, IF
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-ASPA Antibody
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Target
See all ASPA Antibodies
ASPA
(Aspartoacylase (ASPA))
Binding Specificity
All epitopes for ASPA antibodies
AA 39-270
Reactivity
All reactivities for ASPA antibodies
Human
Host
All hosts for ASPA antibodies
Rabbit
Clonality
All clonalities for ASPA antibodies
Polyclonal
Conjugate
All conjugates for ASPA antibodies
This ASPA antibody is un-conjugated
Application
All applications for ASPA antibodies
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
Purification
Purified by antigen-affinity chromatography.
Immunogen
Recombinant protein fragment contain a sequence corresponding to a region within amino acids 39 and 270 of Aspartoacylase
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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 ASPA
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Target
ASPA
(Aspartoacylase (ASPA))
Alternative Name
Aspartoacylase (ASPA Products )
Synonyms
asp antibody, acy2 antibody, ACY-2 antibody, ASP antibody, ACY2 antibody, Acy-2 antibody, Acy2 antibody, nur7 antibody, zgc:171507 antibody, aspartoacylase antibody, Aspartoacylase antibody, ASPA antibody, aspa antibody, Fbal_2465 antibody, Aspa antibody
Background
This gene encodes an enzyme that catalyzes the conversion of N-acetyl_L-aspartic acid (NAA) to aspartate and acetate.NAA is abundant in the brain where hydrolysis by aspartoacylase is thought to help maintain white matter.This protein is an NAA scavenger in other tissues.Mutations in this gene cause Canavan disease.Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq]
Molecular Weight
36 kDa
Gene ID
443
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