Ecscr Antibodies

AND Ecscr ELISA kits, Ecscr Proteins

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

We validate the specificity of these antibodies to Ecscr by testing them on tissues known to express Ecscr positively and negatively. Browse below to find the Ecscr antibody that suites your experiment. We have 0 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.

Previous: Septin9 Next: Tefm

Ecscr Infographic by Boster Bio

All Ecscr Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

Ecscr Overview

Facts about Endothelial cell-specific chemotaxis regulator.

Endothelial cell-specific chemotaxis regulator (Ecscr)

Regulates endothelial chemotaxis and tube formation (By similarity). Has a role in angiogenesis and apoptosis via modulation of the actin cytoskeleton and facilitation of proteasomal degradation of the apoptosis inhibitors BIRC3/IAP1 and BIRC2/IAP2.

Gene Information

Mouse
Gene Name:	Ecscr
Uniprot:	Q3TZW0
Entrez:	68545

Family

Belongs to:

ECSCR family

Alternative Names

Endothelial cell-specific chemotaxis regulator

Molecular Weight

Mass (kDA):
22.689 kDA

Genomic Context


Mouse

Location:	18\|18 B2
Sequence:	18;

Tissue Specificity

Expressed in all tissues examined, highest expression was observed in lung and spleen endothelial cells.

PTMs

Glycoprotein

Phosphoprotein

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

References

PMID: 19416853 by Ikeda K., et al. Identification of ARIA regulating endothelial apoptosis and angiogenesis by modulating proteasomal degradation of cIAP-1 and cIAP- 2.