Adenylosuccinate lyase antibody

Synonyms:Adenylosuccinase antibody, adenylosuccinate lyase antibody, ADSL antibody, AMPS antibody, ASASE antibody, ASL antibody
Catalogue No.:FNab00161Reactivity:Human, Mouse, Rat
Host:RabbitTested Application:ELISA, WB, IHC, IF, FC
Clonality:polyclonalIsotype:IgG
  • SPECIFICATIONS
Product Name
Adenylosuccinate lyase antibody
Catalogue No.
FNab00161
Size
100μg
Form
liquid
Purification
Immunogen affinity purified
Purity
≥95% as determined by SDS-PAGE
Clonality
polyclonal
Isotype
IgG
Storage
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months(Avoid repeated freeze / thaw cycles.)
Immunogen
Immunogen
adenylosuccinate lyase
Alternative Names
Adenylosuccinase antibody, adenylosuccinate lyase antibody, ADSL antibody, AMPS antibody, ASASE antibody, ASL antibody
UniProt ID
P30566
Observed MW
55 kDa
Application
Tested Applications
ELISA, WB, IHC, IF, FC
Recommended dilution
WB: 1:500-1:5000; IHC: 1:20-1:200; IF: 1:10-1:100
Validated Images
HeLa cells were subjected to SDS PAGE followed by western blot with FNab00161(ADSL antibody) at dilution of 1:400
Immunohistochemistry of paraffin-embedded human liver cancer using FNab00161(ADSL antibody) at dilution of 1:50
Background
ADSL(adenylosuccinate lyase) is also named as AMPS, ASase, ASL and belongs to the lyase 1 family. It is an enzyme involved in 2 pathways of purine nucleotide metabolism and catalyzes cleavage of succinyl groups to yield fumarate(PMID:18524658). Defects in ADSL are the cause of adenylosuccinase deficiency(ADSL deficiency). In humans, mutations in ADSL lead to an inborn error of metabolism originally characterized by developmental delay, often with autistic features(PMID:20884265)..The ADSL enzymatic activity is reduced in lymphocytes and red blood cells of the patient with severe psychomotor retardation(PMID:9545543). It has 2 isoforms produced by alternative splicing.