Arylsulfatase L Antibody / ARSL
Arylsulfatase L is an enzyme that, in humans, is encoded by the ARSL gene. It is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the Y chromosome.
Product Specifications
CAS Number
9007-83-4
Specifications
Western blot: 0.5-1 µg/mL
UniProt
P51690
Host
Rabbit
Reactivity
Human, Monkey
Immunogen
Amino acids FYQVMERVQQAVWEHQR from the human protein were used as the immunogen for the Arylsulfatase L antibody.
Clonality
Polyclonal
Isotype
IgG
Applications
WB
Purity
Affinity purified
Format
Antigen affinity purified
Buffer
Lyophilized from 1X PBS with 2% Trehalose and 0.025% sodium azide
Reconstitution
Limitations
This Arylsulfatase L antibody is available for research use only.
Storage Conditions
Formulation
0.5 mg/mL if reconstituted with 0.2ml sterile DI water
Applications Notes
Optimal dilution of the Arylsulfatase L antibody should be determined by the researcher.
Image Legend
Western blot testing of 1) human HEK293, 2) monkey COS-7 and 3) human HK-2 lysate with Arylsulfatase L antibody. Predicted molecular weight ~66 kDa.
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