Recombinant Selectin E/CD62e antibody
Quick Overview for Recombinant Selectin E/CD62e antibody (ABIN8093463)
Target
See all Selectin E/CD62e (SELE) AntibodiesAntibody Type
Reactivity
Host
Clonality
Conjugate
Application
Grade
Clone
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Purpose
- SELE Antibody / E-selectin (azide and preservative free)
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Immunogen
- Prokaryotic recombinant fusion protein corresponding to the cysteine-rich complement control protein domains of the CD62E molecule was used as the immunogen for the SELE/E-selectin antibody.
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Isotype
- IgG1, kappa
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Application Notes
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1. Optimal dilution of the SELE/E-selectin antibody should be determined by the researcher.
2. This SELE/E-selectin antibody is recombinantly produced by expression in CHO cells. -
Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- 1 mg/mL in 1X PBS, BSA free, sodium azide free
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Preservative
- Azide free
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Storage
- -20 °C,-80 °C
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Storage Comment
- SELE/E-selectin antibody with sodium azide - store at 2 to 8oC, antibody without sodium azide - store at -20 to -80oC.
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- Selectin E/CD62e (SELE) (Selectin E (SELE))
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Alternative Name
- SELE
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Background
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SELE antibody, also known as E-selectin antibody, recognizes E-selectin, a type I transmembrane adhesion molecule encoded by the SELE gene and commonly referred to as CD62E and endothelial-leukocyte adhesion molecule 1. E-selectin is primarily localized to the plasma membrane of activated endothelial cells and is a member of the selectin family of calcium-dependent lectins. Under basal conditions, SELE expression is low or absent, however, it is rapidly induced in endothelial cells in response to inflammatory cytokines such as interleukin-1 and tumor necrosis factor alpha, linking vascular activation to immune cell recruitment.
SELE antibody detects a glycoprotein composed of an N-terminal C-type lectin domain, an epidermal growth factor-like domain, multiple short consensus repeat units, a single transmembrane region, and a short cytoplasmic tail. The lectin domain mediates binding to sialylated carbohydrate ligands, including sialyl Lewis x structures on neutrophils, monocytes, and subsets of lymphocytes. Through these interactions, E-selectin supports leukocyte tethering and rolling along the vascular endothelium under shear flow conditions, representing a critical early step in extravasation during inflammation.
Functionally, E-selectin plays a central role in acute and chronic inflammatory responses by regulating leukocyte trafficking into tissues. Because its expression is tightly controlled and transient following cytokine stimulation, SELE is widely used as a marker of endothelial activation in experimental models of vascular inflammation. Elevated E-selectin levels have been associated with atherosclerosis, cardiovascular disease, autoimmune disorders, and other inflammatory conditions. In oncology research, endothelial E-selectin can contribute to adhesion of circulating tumor cells, implicating SELE in metastatic dissemination and tumor-vascular interactions.
The SELE gene is located on chromosome 1 and is transcriptionally regulated by inflammatory signaling pathways, including those downstream of nuclear factor kappa B activation. The endothelial-restricted and inducible nature of E-selectin expression makes detection of this protein valuable for studying cytokine signaling, vascular biology, and immune-endothelial interactions.
This recombinant monoclonal SELE antibody (clone r16G4) targets E-selectin protein in research applications. SELE antibody supports investigation of endothelial activation, leukocyte recruitment mechanisms, and disease-associated inflammatory signaling. -
UniProt
- P16581
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Pathways
- Thromboxane A2 Receptor Signaling
Target
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