Recombinant Rat CXCL1 protein (His Tag)

Species

Rat

Purity

>90 %, SDS-PAGE

Tag

His Tag

Activity

not tested

Cat no : Eg0948



Product Information

Purity >90 %, SDS-PAGE
Endotoxin <0.1 EU/μg protein, LAL method
Activity
Not tested
Expression HEK293-derived Rat CXCL1 protein Ala25-Lys96 (Accession# P14095) with a His tag at the N-terminus.
GeneID 81503
Accession P14095
PredictedSize 8.9 kDa
SDS-PAGE 10-12 kDa, reducing (R) conditions
Formulation Lyophilized from 0.22 μm filtered solution in 20 mM Tris, 150 mM NaCl, pH 7.4. Normally 5% trehalose and 5% mannitol are added as protectants before lyophilization.
Reconstitution Briefly centrifuge the tube before opening. Reconstitute at 0.1-0.5 mg/mL in sterile water.
Storage Conditions
It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
  • Until expiry date, -20℃ to -80℃ as lyophilized proteins.
  • 3 months, -20℃ to -80℃ under sterile conditions after reconstitution.
Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the recommended temperature.

Background

CXC motif chemokine ligand 1 (CXCL1), a CXC chemokine, is also known as growth-regulated (or-related) oncogene-α (Gro-α) and melanoma growth-stimulatory activity (MGSA).It is one of seven chemokines that activate the CXC motif chemokine receptor 2 (CXCR2) and one of the most studied CXC chemokines. CXCL1 is a chemoattractant cytokine. Its most important property is to cause chemotaxis of immune cells, mainly neutrophils, and to a lesser extent CD14+ monocytes and basophils, but not T cells. It also reduces neutrophil apoptosis and thus increases the accumulation of these cells at sites of inflammatory reactions. CXCL1 also causes the chemotaxis of endothelial cells and thus participates in angiogenesis.

References:

1.Hughes. et al. (2018). FEBS J. 285, 2944–2971. 2.Haskill.et al (1990). Proc.Natl. Acad. Sci.87, 7732–7736. 3.Richmond.et al (1985).Cancer Res.45, 6390–6394. 4.Maheshwari.et al (2005).Cytokine. 29, 135–140. 5.Yadav.et al (2019). J.Leukoc.Biol.105, 755–766. 6.Spangler.et al(2013).Genesis. 51, 587–595. 7.Geissmann.et al (2003).Immunity. 19, 71–82. 8.Geiser.et al(1993).J.Biol.Chem. 268, 15419–15424.

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