Serine protease 23 Antibodies

AND PRSS23 ELISA kits, Serine protease 23 Proteins

Many biological assays use antibodies to detect Serine protease 23, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Serine protease 23 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Serine protease 23 antibodies...

We validate the specificity of these antibodies to Serine protease 23 by testing them on tissues known to express PRSS23 positively and negatively. Browse below to find the PRSS23 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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PRSS23 Infographic by Boster Bio

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Anti-PRS23 PRSS23 Antibody

Western blot analysis of lysates from A431 cells, primary antibody was diluted at 1:1000, 4°over night

Human, Mouse, Rat

ELISA, WB

$380
Cat # A11174
100ul

PRSS23 Overview

Facts about Serine protease 23.

PRSS23 3D structure. Source: alphafold

Serine protease 23 (PRSS23)

Gene Information

Human
Gene Name:	PRSS23
Uniprot:	O95084
Entrez:	11098

Family

Belongs to:

peptidase S1 family

Alternative Names

Serine protease 23

Molecular Weight

Mass (kDA):
43.001 kDA

Genomic Context


Human

Location:	11q14.2
Sequence:	11; NC_000011.10 (86791071..86952910)

Subcellular Localizations

Secreted.

PTMs

Disulfide bond

Glycoprotein

Phosphoprotein

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/PRSS23

References

PMID: 11230166 by Wiemann S., et al. Towards a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs.

PMID: 12975309 by Clark H.F., et al. The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment.