Cathepsin A Rabbit Polyclonal Antibody
Catalog #:EAB13788
Host / Isotype Clonality Applications MW (kDa) Reactivity
Rabbit IgG Polyclonal WB, IF/ICC, ELISA 55 Human, Mouse, Rat
Application Key

WB-Western Blot IP-Immunoprecipitation IHC-Immunohistochemistry IF-Immunofluorescence ICC-Immunocytochemistry FC-Flow Cytometry

Reactivity Key

H-Human M-Mouse R-Rat Mk-Monkey B-Bovine Pg-Pig Hm-Hamster Dg-Dog C-Chicken X-Xenopus Z-Zebrafish Hr-Horse All-All Species Expected

Applications Dilutions
The application notes include recommended starting dilutions;optimal dilutions/concentrations should be detemined by the end user.
WB(Westem Blotting)
IHC-P(Immunohistochemistry-Paraffin)
IF/ICC(Immunofluorescence/Immunocytochemistry)
ELISA(Enzyme-linked Immunosorbent Assay)
WB=1:500-2000 
IF/ICC=1:50-300 
Product Information
Conjugate Unconjugate
Specificity Cathepsin A Rabbit Polyclonal Antibody detects endogenous levels of Cathepsin A protein.
Purification Affinity purification
Concentration 1mg/ml
Format Liquid
Formulation In PBS, pH 7.4, containing 0.02% sodium azide,0.5% BSA and 50% glycerol.
Shipping Gel Pack
Storage Store at -20°C least 1 year from the date of shipment. avoid repeated freeze/thaw cycles. Aliquots may be stored at +4°C for 1-2 weeks.
UniProt ID

P10619

Entrez Gene ID

5476

Product Description

Cathepsin A also known as CTSA is a member of the peptidase S10 family of serine carboxypeptidases. Cathepsin A plays a crucial role in lysosomal function by forming a high molecular weight complex with β-galactosidase and α-neuraminidase, thereby protecting these enzymes from degradation within the lysosome. This protective mechanism is vital for maintaining cellular metabolism and ensuring proper peptide biosynthesis and protein degradation. Deficiencies in cathepsin A can lead to a cascade of issues, including the dysfunction of β-galactosidase and α-neuraminidase, which are essential for the breakdown of glycoproteins and glycolipids. The gene encoding human cathepsin A is located on chromosome 20q13.12, and mutations in this gene are associated with galactosialidosis, a lysosomal storage disorder characterized by the accumulation of undegraded substrates due to the deficiencies of these critical enzymes.

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For Research Use Only, Not For Diagnostic Or Therapeutic Procedures.
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