Arylsulfatase L Antibodies

AND ARSL ELISA kits, Arylsulfatase L Proteins

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

We validate the specificity of these antibodies to Arylsulfatase L by testing them on tissues known to express ARSL positively and negatively. Browse below to find the ARSL antibody that suites your experiment. We have 1 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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ARSL Infographic by Boster Bio

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Anti-ARSE/ASE/ARSL Antibody Picoband®

Western blot analysis of ARSE/ASE/ARSL using anti-ARSE/ASE/ARSL antibody (A10294-2)

Human, Monkey

$370
Cat # A10294-2
100 μg/vial

ARSL Overview

Facts about Arylsulfatase L.

ARSL 3D structure. Source: alphafold

Arylsulfatase L (ARSL)

Might be essential for the correct composition of bone and cartilage matrix during development. Has no activity toward steroid sulfates.

Gene Information

Human
Gene Name:	ARSL
Uniprot:	P51690
Entrez:	415

Family

Belongs to:

sulfatase family

Alternative Names

Arylsulfatase L

Molecular Weight

Mass (kDA):
65.669 kDA

Genomic Context


Human

Location:	Xp22.33
Sequence:	X; NC_000023.11 (2934521..2968245, complement)

Tissue Specificity

Expressed in the pancreas, liver and kidney.

Subcellular Localizations

Golgi apparatus, Golgi stack.

Diseases

Chondrodysplasia punctata 1, X-linked recessive (CDPX1)

PTMs

Glycoprotein

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

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: 9497243 by Daniele A., et al. Biochemical characterization of arylsulfatase E and functional analysis of mutations found in patients with X-linked chondrodysplasia punctata.