
Thermo Fisher Scientific Aminoacylase Polyclonal Antibody
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Applications
Tested Dilution
Publications
Western Blot (WB)
0.1 µg/mL
Immunoprecipitation (IP)
25 µg/mL
Product Specifications
Species Reactivity
Mouse
Host/Isotype
Goat / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Mouse myeloma cell line NS0-derived recombinant mouse Aminoacylase/ACY1 Met1-Ser408 if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
Aminoacylase,
uniProtId:
Q99JW2-1,
ncbiNodeId:
10090,
antigenRange:
1-408,
antigenLength:
408,
antigenImageFileName:
PA5-47371_Aminoacylase_Q99JW2-1_Goat.svg,
antigenImageFileNamePDP:
PA5-47371_Aminoacylase_Q99JW2-1_Goat_PDP.jpeg,
sortOrder:
2}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Lyophilized
Concentration
0.2 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
PBS with 5% trehalose
Contains
No Preservative
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2605808
Product Specific Information
In direct ELISAs and Western blots, approximately 50% cross-reactivity with recombinant human Aminoacylase/ACY1 is observed.
Reconstitute at 0.2 mg/mL in sterile PBS.
Target Information
ACY1 encodes a cytosolic, homodimeric, zinc-binding enzyme that catalyzes the hydrolysis of acylated L-amino acids to L-amino acids and an acyl group, and has been postulated to function in the catabolism and salvage of acylated amino acids. This gene is located on chromosome 3p21. 1, a region reduced to homozygosity in small-cell lung cancer (SCLC), and its expression has been reported to be reduced or undetectable in SCLC cell lines and tumors. The amino acid sequence of human aminoacylase-1 is highly homologous to the porcine counterpart, and this enzyme is the first member of a new family of zinc-binding enzymes. Mutations in this gene cause aminoacylase-1 deficiency, a metabolic disorder characterized by central nervous system defects and increased urinary excretion of N-acetylated amino acids. Alternative splicing of this gene results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ABHD14A (abhydrolase domain containing 14A) gene. A related pseudogene has been identified on chromosome 18.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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