Recombinant Mouse CXCL1/KC (aa 29-96) Protein
Recombinant Mouse CXCL1/KC (aa 29-96) Protein Summary
Product Specifications
Asn29-Lys96
Analysis
Product Datasheets
Carrier Free
CF stands for Carrier Free (CF). We typically add Bovine Serum Albumin (BSA) as a carrier protein to our recombinant proteins. Adding a carrier protein enhances protein stability, increases shelf-life, and allows the recombinant protein to be stored at a more dilute concentration. The carrier free version does not contain BSA.
In general, we advise purchasing the recombinant protein with BSA for use in cell or tissue culture, or as an ELISA standard. In contrast, the carrier free protein is recommended for applications, in which the presence of BSA could interfere.
1395-KC
Formulation | Lyophilized from a 0.2 μm filtered solution in PBS with BSA as a carrier protein. |
Reconstitution | Reconstitute at 100 μg/mL in sterile PBS containing at least 0.1% human or bovine serum albumin. |
Shipping | The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. |
Stability & Storage: | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
|
1395-KC/CF
Formulation | Lyophilized from a 0.2 μm filtered solution in PBS. |
Reconstitution | Reconstitute at 100 μg/mL in sterile PBS. |
Shipping | The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. |
Stability & Storage: | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
|
Reconstitution Calculator
Background: CXCL1/GRO alpha/KC/CINC-1
CXCL1, also known as KC, GRO alpha, and CINC-1, is an approximately 8 kDa proinflammatory chemokine that plays a key role in neutrophil migration and activation (1). Mature mouse CXCL1 shares 64% and 92% aa sequence identity with human and rat CXCL1, respectively [oquendo 4133, ryseck 266, cochran 939]. It is produced by many cell types in inflammatory sites and during chronic inflammatory diseases (1). CXCL1 can associate into bioactive dimers and primarily signals through CXCR2/IL-8 RB but can also bind with lower affinity to CXCR2/IL-8 RA (5-7). It induces neutrophil migration, extravasation, respiratory burst, and degranulation and also induces T cells to produce proinflammatory IL-17 (6, 8, 9). CXCL1 additionally binds to Syndecan-1 on epithelial cells which acts as a sink for CXCL1 activity until Syndecan-1 cleavage by MMP-7 (10). CXCL1 is up-regulated in spinal cord astrocytes by inflammatory stimuli or tumor cell injection, and it exacerbates pain sensation by potentiating excitatory NMDA neurotransmission (11, 12). In the circulatory system, CXCL1 interacts with CXCR2 on endothelial cells to promote lymphatic tube formation and angiogenesis (13, 14). It promotes the hypertrophic differentiation of chondrocytes resulting in cartilage matrix deposition, calcification, and remodeling (15). It interacts with both CXCR1 and CXCR2 on adipose stromal cells and promotes their recruitment to prostate tumors in obese patients (16). It also binds CXCR2 on ovarian cancer cells, leading to cleavage of cell surface HB-EGF, transactivation of EGF R, and cell proliferation (17).
- Strieter, R.M. et al. (2005) Cytokine Growth Factor Rev. 16:593.
- Cochran, B.H. et al. (1983) Cell 33:939.
- Oquendo, P. et al. (1989) J. Biol. Chem. 264:4133.
- Ryseck, R.P. et al. (1989) Exp. Cell Res. 180:266.
- Sawant, K.V. et al. (2015) J. Innate Immun. 7:647.
- Geiser, T. et al. (1993) J. Biol. Chem. 268:15419.
- Ahuja, S.K. and P.M. Murphy (1996) J. Biol. Chem. 271:20545.
- Jin, L. et al. (2014) J. Immunol. 193:3549.
- De Filippo, K. et al. (2013) Blood 121:4930.
- Gill, S.E. et al. (2016) Am. J. Respir. Cell. Mol. Biol. PMID 26934670.
- Cao, D.-L. et al. (2014) Exp. Neurol. 261:328.
- Xu, J. et al. (2014) J. Neuroinflamm. 11:38.
- Xu, J. et al. (2012) Int. J. Cancer 130:787.
- Miyake, M. et al. (2013) Lab. Invest. 93:768.
- Merz, D. et al. (2003) J. Immunol. 171:4406.
- Zhang, T. et al. (2016) Nat. Commun. 7:11674.
- Bolitho, C. et al. (2010) Endocr. Relat. Cancer 17:929.
Citation for Recombinant Mouse CXCL1/KC (aa 29-96) Protein
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
1 Citation: Showing 1 - 1
-
Transepithelial migration of neutrophils into the lung requires TREM-1.
Authors: Klesney-Tait, Julia, Keck, Kathy, Li, Xiaopeng, Gilfillan, Susan, Otero, Karel, Baruah, Sankar, Meyerholz, David K, Varga, Steven M, Knudson, Cory J, Moninger, Thomas O, Moreland, Jessica, Zabner, Joseph, Colonna, Marco
J Clin Invest, 2012-12-17;123(1):138-49.
Species: Mouse
Sample Types: Whole Cells
Applications: Bioassay
FAQs
No product specific FAQs exist for this product, however you may
View all Proteins and Enzyme FAQsReviews for Recombinant Mouse CXCL1/KC (aa 29-96) Protein
There are currently no reviews for this product. Be the first to review Recombinant Mouse CXCL1/KC (aa 29-96) Protein and earn rewards!
Have you used Recombinant Mouse CXCL1/KC (aa 29-96) Protein?
Submit a review and receive an Amazon gift card.
$25/€18/£15/$25CAN/¥75 Yuan/¥2500 Yen for a review with an image
$10/€7/£6/$10 CAD/¥70 Yuan/¥1110 Yen for a review without an image