CD162

Item Information
Catalog #
Size
Price
Description

This gene encodes a glycoprotein that functions as a high affinity counter-receptor for the cell adhesion molecules P-, E- and L- selectin expressed on myeloid cells and stimulated T lymphocytes. As such, this protein plays a critical role in leukocyte trafficking during inflammation by tethering of leukocytes to activated platelets or endothelia expressing selectins. This protein requires two post-translational modifications, tyrosine sulfation and the addition of the sialyl Lewis x tetrasaccharide (sLex) to its O-linked glycans, for its high-affinity binding activity. Aberrant expression of this gene and polymorphisms in this gene are associated with defects in the innate and adaptive immune response. Alternate splicing results in multiple transcript variants.

Product Overview
Entrez GenelD
6404
Aliases
CLA; SELPLG; PSGL1; PSGL-1
Clone#
3D5E11
Host / Isotype
Mouse / Mouse IgG1
Species Reactivity
Human
Immunogen
Purified recombinant fragment of human CD162 (AA: 42-320) expressed in E. Coli.
Formulation
Purified antibody in PBS with 0.05% sodium azide
Storage
4℃; -20℃ for long term storage
Product Applications
WB (Western Blot)
1/500 - 1/2000
IHC_P(Immunohistochemistry)
1/200 - 1/1000
FCM (Flow Cytometry)
1/200 - 1/400
ELISA
1/10000
References
1.World J Gastroenterol. 2020 Nov 7;26(41):6361-6377.
2.Nat Microbiol. 2019 May;4(5):813-825.
Product Image
Elisa
Figure 1:Black line: Control Antigen (100 ng);Purple line: Antigen (10ng); Blue line: Antigen (50 ng); Red line:Antigen (100 ng)
Figure 1:Black line: Control Antigen (100 ng);Purple line: Antigen (10ng); Blue line: Antigen (50 ng); Red line:Antigen (100 ng)
Western Blot
Figure 2:Western blot analysis using CD162 mAb against human CD162 (AA: 42-320) recombinant protein. (Expected MW is 54.7 kDa)
Figure 2:Western blot analysis using CD162 mAb against human CD162 (AA: 42-320) recombinant protein. (Expected MW is 54.7 kDa)
Immunohistochemical analysis
Figure 4:Immunohistochemical analysis of paraffin-embedded cerebellum tissues using CD162 mouse mAb with DAB staining.
Figure 4:Immunohistochemical analysis of paraffin-embedded cerebellum tissues using CD162 mouse mAb with DAB staining.
Immunohistochemical analysis
Figure 5:Immunohistochemical analysis of paraffin-embedded rectum cancer tissues using CD162 mouse mAb with DAB staining.
Figure 5:Immunohistochemical analysis of paraffin-embedded rectum cancer tissues using CD162 mouse mAb with DAB staining.
Immunofluorescence analysis
Figure 5:Flow cytometric analysis of THP-1 cells using CD162 mouse mAb (green) and negative control (red).
Figure 5:Flow cytometric analysis of THP-1 cells using CD162 mouse mAb (green) and negative control (red).
For Research Use Only. Not for use in diagnostic procedures.