Arylsulfatase D Antibodies

AND ARSD ELISA kits, Arylsulfatase D Proteins

Many biological assays use antibodies to detect Arylsulfatase D, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Arylsulfatase D in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Arylsulfatase D antibodies...

We validate the specificity of these antibodies to Arylsulfatase D by testing them on tissues known to express ARSD positively and negatively. Browse below to find the ARSD antibody that suites your experiment. We have 4 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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ARSD Infographic by Boster Bio

All ARSD Products

Product

Figures

Specificity

Applications

Price

Anti-Arylsulfatase D ARSD Antibody

Human, Mouse

$405
Cat # A08673
100ul

Anti-Arylsulfatase D ARSD Antibody

Human

ELISA, IF, IHC

$380
Cat # A08673-1
100ul

Arylsulfatase D (ARSD) (NM_001669) Human Recombinant Protein

$1249
Cat # PROTP51689
20 µg

Arylsulfatase D (ARSD) (NM_001669) Human Over-expression Lysate

Human

$628
Cat # LS000414
100 µg

ARSD Overview

Facts about Arylsulfatase D.

ARSD 3D structure. Source: alphafold

Arylsulfatase D (ARSD)

Gene Information

Human
Gene Name:	ARSD
Uniprot:	P51689
Entrez:	414

Family

Belongs to:

sulfatase family

Alternative Names

arylsulfatase D; ASD; EC 3.1.6.-; EC 3.1.6.2

Molecular Weight

Mass (kDA):
64.86 kDA

Genomic Context


Human

Location:	Xp22.33
Sequence:	X; NC_000023.11 (2903972..2929345, complement)

Tissue Specificity

Expressed in the pancreas, kidney, liver, lung, placenta, brain and heart.

Subcellular Localizations

Lysosome.

Diseases

Rett Syndrome
Scoliosis, Unspecified
Adolescent Idiopathic Scoliosis
Steroid Sulfatase Deficiency Disease
Malignant Neoplasms
Torsion Abnormality
Submersion
Kidney Calculi
Leukemia
Chondrodysplasia Punctata
Fetal Warfarin Syndrome
Lung Diseases

Acquired Kyphosis
Lung Diseases, Obstructive
Endometriosis, Site Unspecified
Acute Promyelocytic Leukemia
Poultry Diseases
Dwarfism

Pathways

Transport
Pathogenesis
Localization
Excretion
Secretion
Bioluminescence
Methylation
Transposition

Translation
Male Meiosis
Meiosis

PTMs

Glycoprotein

Research Areas

Lipid and Metabolism

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/ARSD

References

PMID: 7720070 by Franco B., et al. A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy.

PMID: 11177574 by Urbitsch P., et al. Arylsulfatase D gene in Xp22.3 encodes two protein isoforms.