Antibody Protein ELISA Kit from MyBioSource header Telephone 1.858.633.0165          
1.855.MyBioSource
Fax 1.858.633.0166    Email sales@mybiosource.com 
tel/fax
menu1 Home Products Ordering Company Help menu7
bottom
   MyBioSource  rightarrow Protein Family  rightarrow Arylsulfatase  rightarrow LOG IN  rightarrow MY ACCOUNT  rightarrow CART CONTENTS  rightarrow CHECKOUT 
horiz bar
MyBioSource Menu separator
separator
ELISA Kit ELISA Kit
CLIA Kit CLIA Kit
PCR Kit PCR Kit
Monoclonal Antibody Monoclonal Antibody
Polyclonal Antibody Polyclonal Antibody
Secondary Antibody Secondary Antibody
Antigen Antigen
Biochemical Biochemical
cDNA Clone cDNA Clone
siRNA siRNA
Peptide Peptide
Recombinant/Purified Protein Rec./Purified Protein

Custom ELISA Kit Custom ELISA Kit
Custom Protein Custom Protein
Custom Antibody Custom Antibody
Antibody Matched Pairs Antibody Matched Pairs
Antibody & Corresponding Blocking Peptide Pairs Antibody Peptide Pairs
Phospho-Specific Antibodies Phospho Antibodies
Products by Disease Products by Disease
Products by Pathway Products by Pathway
Products by Tissue Products by Tissue

arrow Advanced Search
arrow Submit Technical Q&A
arrow International Distributors
arrow Contact Us
separator
Our Best Sellers moreseparator
separator
 • Androgen Receptor (Ab-94) (AR) Antibody
 • ACOT1 Antibody
 • Connexin 31 (CX31) ELISA Kit
 • Choline Acetylase (CHAC) ELISA Kit
 • beta-Hexosaminidase A (beta-HEX A) ELISA Kit
 • Caspase 3 (CASPASE-3) ELISA Kit
 • Cluster of Differentiation 74 (CD74) ELISA Kit
 • Ovarian Cancer Marker-Carbohydrate Antigen 125 (OCM-CA125) ELISA Kit
 • Growth Differentiation Factor 15 (GDF15) ELISA Kit
 • Platelet Derived Growth Factor D (PDGFD) ELISA Kit
 • Vimentin ELISA Kit
 • Creatine Kinase, Mitochondrial 1B (CKMT1B) ELISA Kit
 • Chromobox Homolog 3 (CBX3) ELISA Kit
 • Mucin 4 (MUC4) ELISA Kit
 downarrow more ...
separator

Arylsulfatase

separator
Is commonly produced by soil microorganisms and plays an important role in the mineralization of sulfates.

Below are the list of possible Arylsulfatase products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Arylsulfatase

 Arylsulfatase ELISA Kit
 Arylsulfatase Recombinant
 Arylsulfatase Antibody
Also known as Arylsulfatase (AS) (Aryl-sulfate sulphohydrolase).
Is commonly produced by soil microorganisms and plays an important role in the mineralization of sulfates.
Table BarTOPTable Bar
 

Arylsulfatase A

 Arylsulfatase A ELISA Kit
 Arylsulfatase A Recombinant
 Arylsulfatase A Antibody
Also known as Arylsulfatase A (ASA) (Cerebroside-sulfatase).
ARSA: Hydrolyzes cerebroside sulfate. Defects in ARSA are a cause of leukodystrophy metachromatic (MLD). MLD is a disease due to a lysosomal storage defect. It is characterized by intralysosomal storage of cerebroside-3-sulfate in neural and non-neural tissues, with a diffuse loss of myelin in the central nervous system. Progressive d
>>>
emyelination causes a variety of neurological symptoms, including gait disturbances, ataxias, optical atrophy, dementia, seizures, and spastic tetraparesis. Three forms of the disease can be distinguished according to the age at onset: late- infantile, juvenile and adult. Arylsulfatase A activity is defective in multiple sulfatase deficiency (MSD). A clinically and biochemically heterogeneous disorder caused by the simultaneous impairment of all sulfatases, due to defective post-translational modification and activation. It combines features of individual sulfatase deficiencies such as metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata, hydrocephalus, ichthyosis, neurologic deterioration and developmental delay. Arylsulfatase A activity is impaired in multiple sulfatase deficiency due to mutations in SUMF1. SUMF1 mutations result in defective post-translational modification of ARSA at residue Cys- 69 that is not converted to 3-oxoalanine. Belongs to the sulfatase family.

Protein type: EC 3.1.6.8; Hydrolase; Lipid Metabolism - sphingolipid

Chromosomal Location of Human Ortholog: 22q13.33

Cellular Component: endoplasmic reticulum lumen; lysosomal lumen; lysosome

Molecular Function: arylsulfatase activity; calcium ion binding; cerebroside-sulfatase activity; protein binding; sulfuric ester hydrolase activity

Biological Process: glycosphingolipid metabolic process; post-translational protein modification

Disease: Metachromatic Leukodystrophy
 ARSA ELISA Kit
 ARSA Recombinant
 ARSA Antibody
Table BarTOPTable Bar
 

Arylsulfatase B

 Arylsulfatase B ELISA Kit
 Arylsulfatase B Recombinant
 Arylsulfatase B Antibody
Also known as Arylsulfatase B (ASB) (N-acetylgalactosamine-4-sulfatase) (G4S).
ARSB: Defects in ARSB are the cause of mucopolysaccharidosis type 6 (MPS6); also known as Maroteaux-Lamy syndrome. MPS6 is an autosomal recessive lysosomal storage disease characterized by intracellular accumulation of dermatan sulfate. Clinical features can include abnormal growth, short stature, stiff joints, skeletal malformations, corneal clouding, hepatosplenomegaly, and cardiac abnormalities. A wide variation in clinical severity is observed. Arylsulfatase B activity is defective in multiple sulfatase defic
>>>
iency (MSD). A clinically and biochemically heterogeneous disorder caused by the simultaneous impairment of all sulfatases, due to defective post-translational modification and activation. It combines features of individual sulfatase deficiencies such as metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata, hydrocephalus, ichthyosis, neurologic deterioration and developmental delay. Arylsulfatase B activity is impaired in multiple sulfatase deficiency due to mutations in SUMF1. SUMF1 mutations result in defective post-translational modification of ARSB at residue Cys- 91 that is not converted to 3-oxoalanine. Belongs to the sulfatase family. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: EC 3.1.6.12; Glycan Metabolism - glycosaminoglycan degradation; Hydrolase

Cellular Component: cell surface; Golgi apparatus; lysosome; mitochondrion; rough endoplasmic reticulum

Molecular Function: arylsulfatase activity; N-acetylgalactosamine-4-sulfatase activity; sulfuric ester hydrolase activity

Biological Process: autophagy; central nervous system development; response to estrogen stimulus; response to methylmercury; response to nutrient; response to pH
 Arsb ELISA Kit
 Arsb Recombinant
 Arsb Antibody
 As1 ELISA Kit
 As1 Recombinant
 As1 Antibody
 As1-s ELISA Kit
 As1-s Recombinant
 As1-s Antibody
Table BarTOPTable Bar
 

Arylsulfatase D

 Arylsulfatase D ELISA Kit
 Arylsulfatase D Recombinant
 Arylsulfatase D Antibody
Also known as Arylsulfatase D (ASD).
ARSD: is a member of the sulfatase family. Sulfatases are essential for the correct composition of bone and cartilage matrix. The encoded protein is postranslationally glycosylated and localized to the lysosome. This gene is located within a cluster of similar arylsulfatase genes on chromosome X. A related pseudogene has been identified in the pseudoautosoma
>>>
l region of chromosome Y. [provided by RefSeq, Jul 2011]

Protein type: EC 3.1.6.-; Hydrolase

Chromosomal Location of Human Ortholog: Xp22.3

Cellular Component: endoplasmic reticulum lumen

Molecular Function: arylsulfatase activity

Biological Process: glycosphingolipid metabolic process; post-translational protein modification
 ARSD ELISA Kit
 ARSD Recombinant
 ARSD Antibody
Table BarTOPTable Bar
 

Arylsulfatase E

 Arylsulfatase E ELISA Kit
 Arylsulfatase E Recombinant
 Arylsulfatase E Antibody
Also known as Arylsulfatase E (ASE).
ARSE: May be essential for the correct composition of cartilage and bone matrix during development. Has no activity toward steroid sulfates. Defects in ARSE are the cause of chondrodysplasia punctata X-linked recessive type 1 (CDPX1). CDP is a clinically and genetically heterogeneous disorder characterized by punctiform calcification of the bones. CDPX1 is a
>>>
congenital defect of bone and cartilage development characterized by aberrant bone mineralization, severe underdevelopment of nasal cartilage, and distal phalangeal hypoplasia. This disease can also be induced by inhibition with the drug warfarin. Belongs to the sulfatase family.

Protein type: EC 3.1.6.-; Hydrolase

Chromosomal Location of Human Ortholog: Xp22.3

Cellular Component: endoplasmic reticulum lumen

Molecular Function: arylsulfatase activity

Biological Process: glycosphingolipid metabolic process; post-translational protein modification; skeletal development

Disease: Chondrodysplasia Punctata 1, X-linked Recessive
 ARSE ELISA Kit
 ARSE Recombinant
 ARSE Antibody
Table BarTOPTable Bar
 

Arylsulfatase F

 Arylsulfatase F ELISA Kit
 Arylsulfatase F Recombinant
 Arylsulfatase F Antibody
Also known as Arylsulfatase F (ASF).
ARSF: a member of the sulfatase family, and more specifically, the arylsulfatase subfamily. Members of the subfamily share similarity in sequence and splice sites, and are clustered together on chromosome X, suggesting that they are derived from recent gene duplication events. Sulfatases are essential for the correct composition of bone and cartilage matrix.
>>>
The activity of this protein, unlike that of arylsulfatase E, is not inhibited by warfarin. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Jan 2011]

Protein type: EC 3.1.6.-; Hydrolase; Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: Xp22.3

Cellular Component: endoplasmic reticulum lumen

Molecular Function: arylsulfatase activity

Biological Process: glycosphingolipid metabolic process; post-translational protein modification
 ARSF ELISA Kit
 ARSF Recombinant
 ARSF Antibody
Table BarTOPTable Bar
 

Arylsulfatase G

 Arylsulfatase G ELISA Kit
 Arylsulfatase G Recombinant
 Arylsulfatase G Antibody
Also known as Arylsulfatase G (ASG).
ARSG: Displays arylsulfatase activity at acidic pH with pseudosubstrates, such as p-nitrocatechol sulfate and also, but with lower activity, p-nitrophenyl sulfate and 4- methylumbelliferyl sulfate. Belongs to the sulfatase family.

Protein type: EC 3.1.6.-; Endoplasmic reticulum; Hydrolase; Kinase, other; Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 17q24.2

Cellular Component: endoplasmic reticulum; endoplasmic reticulum lumen; extracellular space; lysosome

Molecular Function: arylsulfatase activit
>>>
y

Biological Process: glycosphingolipid metabolic process; post-translational protein modification; sulfur metabolic process
 ARSG ELISA Kit
 ARSG Recombinant
 ARSG Antibody
 KIAA1001 ELISA Kit
 KIAA1001 Recombinant
 KIAA1001 Antibody
 UNQ839/PRO1777 ELISA Kit
 UNQ839/PRO1777 Recombinant
 UNQ839/PRO1777 Antibody
Table BarTOPTable Bar
 

Arylsulfatase H

 Arylsulfatase H ELISA Kit
 Arylsulfatase H Recombinant
 Arylsulfatase H Antibody
Also known as Arylsulfatase H (ASH).
 ARSH ELISA Kit
 ARSH Recombinant
 ARSH Antibody
Table BarTOPTable Bar
 

Arylsulfatase I

 Arylsulfatase I ELISA Kit
 Arylsulfatase I Recombinant
 Arylsulfatase I Antibody
Also known as Arylsulfatase I (ASI).
ARSI: Displays arylsulfatase activity at neutral pH, when co- expressed with SUMF1; arylsulfatase activity is measured in the secretion medium of retinal cell line, but no activity is recorded when measured in cell extracts. Belongs to the sulfatase family. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: Calcium-bin
>>>
ding; EC 3.1.6.-; Hydrolase; Secreted; Secreted, signal peptide
 Arsi ELISA Kit
 Arsi Recombinant
 Arsi Antibody
Table BarTOPTable Bar
 

Arylsulfatase J

 Arylsulfatase J ELISA Kit
 Arylsulfatase J Recombinant
 Arylsulfatase J Antibody
Also known as Arylsulfatase J (ASJ).
ARSJ: Belongs to the sulfatase family

Protein type: EC 3.1.6.-; Hydrolase; Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 4q26

Cellular Component: endoplasmic reticulum lumen

Molecular Function: arylsulfatase activity

Biological Process: glycosphingolipid metabolic process; post-translational pro
>>>
tein modification
 ARSJ ELISA Kit
 ARSJ Recombinant
 ARSJ Antibody
 UNQ372/PRO708 ELISA Kit
 UNQ372/PRO708 Recombinant
 UNQ372/PRO708 Antibody
Table BarTOPTable Bar
 

Arylsulfatase K

 Arylsulfatase K ELISA Kit
 Arylsulfatase K Recombinant
 Arylsulfatase K Antibody
Also known as Arylsulfatase K (ASK).
 arsk ELISA Kit
 arsk Recombinant
 arsk Antibody
 zgc:153019 ELISA Kit
 zgc:153019 Recombinant
 zgc:153019 Antibody
Table BarTOPTable Bar
Proteins Root Name Listing
horiz bar
 SSL   Follow us on Facebook Follow us onTwitter Follow us on Google Plus Connect us on LinkedIn Subscribe to our RSS Feed for latest products and special promotions