GRO-alpha/CXCL1 Protein, Human (HEK293, His)
Based on 4 publication(s) in Google Scholar
CXCL1 (Chemokine (C-X-C motif) ligand 1), also known as GRO alpha, NAP-3 or MGSA, belongs to the sub-family of CXC chemokine. CXCL1 is involved in the development of many inflammatory diseases, including the induction of angiogenesis and recruitment of neutrophils. CXCL1 is produced by many cell types, and activates CXCR2 and, at high levels, CXCR1. GRO-alpha/CXCL1 Protein, Human (HEK293, His) is produced in HEK293 cells with a C-Terminal His-tag. It consists of 73 amino acids (A35-N107).
- Species: Human
- Source: HEK293
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Storage:Stored at -20°C for 2 years from date of receipt. After reconstitution, it is stable at 4°C for 1 week or -20°C for longer (with carrier protein). It is recommended to freeze aliquots at -20°C or -80°C for extended storage.
Biological Activity
Description
CXCL1 (Chemokine (C-X-C motif) ligand 1), also known as GRO alpha, NAP-3 or MGSA, belongs to the sub-family of CXC chemokine. CXCL1 is involved in the development of many inflammatory diseases, including the induction of angiogenesis and recruitment of neutrophils. CXCL1 is produced by many cell types, and activates CXCR2 and, at high levels, CXCR1[1]. GRO-alpha/CXCL1 Protein, Human (HEK293, His) is produced in HEK293 cells with a C-Terminal His-tag. It consists of 73 amino acids (A35-N107).
Background
CXCL1, also known as GRO-α, is a polypeptide that is initially isolated from human melanoma cells. CXCL1 acts as a key chemoattractant for neutrophils by binding specifically to its corresponding G-protein-coupled receptor CXCR2. CXCL1 modulates angiogenesis, tumorigenesis, and wound healing. In general, CXCL1 levels are extremely low under normal physiological conditions and greatly increased during inflammatory conditions[2][3].
The amino acid sequence of human CXCL1 protein has low homology between mouse and rat CXCL1 protein.
After translation, the synthesized CXCL1 precursor is 107aa long. A signal peptide is removed from its N-terminus, which shortens the precursor to 73aa. Two other amino acids can also be removed from the C-terminus. In addition, two disulfide bridges are formed from all four cysteine residues in CXCL1. The disulfide bridges give the appropriate structure to CXCL1, which determines the properties of this chemokine. After secretion, CXCL1 undergoes further proteolytic processing, which regulates the activity of this chemokine. From the N-terminus, three, four or five amino acids are removed, which produce CXCL1(4-73), CXCL1(5-73), and CXCL1(6-73), respectively. This increases CXCL1 activity 30 times, as measured by its ability to induce the chemotaxis of treated cells. To date, three CXCL1 receptors have been discovered-CXCR1, CXCR2 and atypical chemokine receptor 1 (ACKR1). Through NF-κB activation, CXCL1 expression is increased by cytokines such as IL-1β, TNF-α and IL-17. CXCL1 can associate into bioactive dimers and primarily signals through CXCR2/IL-8 RB[1].
After CXCL1 expression is induced by carcinogens, it participates in inflammatory responses by recruiting neutrophils. This leads to chronic inflammation. In addition to increasing proliferation, CXCL1 also induces cancer cell migration, particularly EMT. Produced by lymphatic endothelial cells (LECs), CXCL1 enables tumor cell migration into the lymphatic vessels during lymphangiogenesis, leading to lymph node metastasis. CXCL1 is a chemotactic factor for neutrophils. Additionally, it causes the mobilization of these cells from the bone marrow. CXCL1 can also induce recruitment of regulatory T cells (Treg) and MSCs into the tumor niche. Another no-less-important property of CXCL1 is its ability to induce angiogenesis[1].
In Vitro
Recombinant human CXCL1 (0, 1, 5, and 10 ng/mL; 6-24 h) promotes IL-6 expression in a dose- and time-dependent manner, and triggers the transcriptional activities of c-Jun in human primary synovial fibroblasts[2].
Recombinant human CXCL1 (50 and 100 ng/mL; 16 h) significantly induces HUVEC proliferation in a concentration-dependent manner[3].
Verified Bioactivity
1.Measured in a cell proliferation assay using HUVEC cells.The ED50 for this effect is 3.689 ng/mL, corresponding to a specific activity is 2.71×105U/mg.
2.Determined by its ability to chemoattract BaF3 mouse pro-B cells transfected with human CXCR2. The ED50 for this effect is 3.516 ng/mL, corresponding to a specific activity is 2.84×105 U/mg.
3.Measured by its binding ability in a functional ELISA. Immobilized Human CXCL1 0.5 μg/mL (100 μL/well) can bind Eltrekibart (HY-P990737). The ED50 for this effect is 19.68 ng/mL.
MCE Validation Data
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Purity - SDS-PAGE
Purity - SDS-PAGE
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Bioactivity - Cell-Based Assay
Bioactivity - Cell-Based Assay
Publications (4)
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Journal Impact Factor
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Most Recent
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Immunity
Spatiotemporal dynamics of CXCL10 encode contextual immune information revealed by the genetically encoded fluorescent sensor. [Abstract]2025 Sep 9;58(9):2320-2335.e9. PMID: 40818452 -
Adv Sci (Weinh)
Single-Cell Landscape of Bronchoalveolar Lavage Fluid Identifies Specific Neutrophils during Septic Immunosuppression. [Abstract]2025 Mar;12(11):e2406218. PMID: 39887584 -
Cell Rep
Collagen 1-mediated CXCL1 secretion in tumor cells activates fibroblasts to promote radioresistance of esophageal cancer. [Abstract]2023 Oct 17;42(10):113270. PMID: 37851572
GRO-alpha/CXCL1 Protein, Human (HEK293, His) purchased from MedChemExpress. Usage Cited in: Cell Rep. 2023 Oct 17;42(10):113270. [Abstract]
Western blot analysis of myCAF- and iCAF-related markers in fibroblasts treated with indicated concentration of GRO-alpha/CXCL1 Protein, Human for 24 h.
GRO-alpha/CXCL1 Protein, Human (HEK293, His) purchased from MedChemExpress. Usage Cited in: Cell Rep. 2023 Oct 17;42(10):113270. [Abstract]
Representative images of fibroblasts migration caused by indicated concentration of GRO-alpha/CXCL1 Protein, Human.
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Cancer Sci
Tumor-Associated Macrophage-Derived CXCL1 Promotes Endometrial Cancer Progression Through the CXCR2/NF-κB Pathway. [Abstract]2026 Jan 17. PMID: 41548046
GRO-alpha/CXCL1 Protein, Human (HEK293, His) purchased from MedChemExpress. Usage Cited in: Cancer Sci. 2026 Jan 17. [Abstract]
epresentative western blotting images of EMT markers in EC cells treated with different concentrations of rCXCL1.
GRO-alpha/CXCL1 Protein, Human (HEK293, His) purchased from MedChemExpress. Usage Cited in: Cancer Sci. 2026 Jan 17. [Abstract]
Proliferative capability of EC cells treated with rCXCL1 (20 and 40 ng/mL) assessed by CCK8 assay.
GRO-alpha/CXCL1 Protein, Human (HEK293, His) purchased from MedChemExpress. Usage Cited in: Cancer Sci. 2026 Jan 17. [Abstract]
Translocation of NF‐κB from the cytoplasm to the nucleus was detected using immunofluorescence to indicate the activation of NF‐κB signaling in EC cells transfected with or without shCXCR2 under conditions of either co‐culture or rCXCL1 treatment.
Technical Parameters
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Species Human
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Source HEK293
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Tag C-6*His
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Accession
P09341 (A35-N107)
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Molecular Construction
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N-term
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CXCL1 (A35-N107)
Accession # P09341 -
6*His
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C-term
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Protein Length
Full Length of Mature Protein
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Synonyms
CXCL1; Neutrophil-Activating Protein 3; Prev. GRO1; Fibroblast Secretory Protein; Prev. MGSA; C-X-C Motif Chemokine 1; Prev. FSP; GRO-Alpha(1-73); SCYB1; GRO1 Oncogene (Melanoma Growth-Stimulating Activity); NAP-3; Melanoma Growth Stimulatory Activity Alpha; MGSA-A; Melanoma Growth Stimulatory Activity; GROa; MGSA Alpha; Chemokine (C-X-C Motif) Ligand 1 (Melanoma Growth Stimulating Activity, Alpha); GROA; GRO1 Oncogene (Melanoma Growth Stimulating Activity, Alpha); GRO; Melanoma Growth Stimulating Activity, Alpha; C-X-C Motif Chemokine Ligand 1; Growth-Regulated Alpha Protein
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AA Sequence
ASVATELRCQCLQTLQGIHPKNIQSVNVKSPGPHCAQTEVIATLKNGRKACLNPASPIVKKIIEKMLNSDKSN
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Predicted Molecular Mass
7.9 kDa
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Molecular Weight
Approximately 11-15 kDa, based on SDS-PAGE under reducing conditions.
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Purity
≥ 95%, as determined by reducing SDS-PAGE.
Product Properties
Lyophilized powder
Lyophilized from a 0.2 μm filtered solution of 20 mM PB, 150 mM NaCl, 5-8% Trehalose, pH 7.4.
<1 EU/μg, determined by LAL method.
It is not recommended to reconstitute to a concentration less than 100 μg/mL in ddH2O.
Stored at -20°C for 2 years from date of receipt. After reconstitution, it is stable at 4°C for 1 week or -20°C for longer (with carrier protein). It is recommended to freeze aliquots at -20°C or -80°C for extended storage.
Room temperature in continental US; may vary elsewhere.
Documentation
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Data Sheet (265 KB)
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SDS (254 KB)
- English - EN (254 KB)
- Français - FR (254 KB)
- Deutsch - DE (254 KB)
- Norwegian - NO (254 KB)
- Español - ES (254 KB)
- Swedish - SV (254 KB)
- Italian - IT (254 KB)
- Korean - KR (254 KB)
- Portuguese - PT (254 KB)
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Handling Instructions (2659 KB)
References
[1]. Giovanna Vella, et al. The IL-17 receptor IL-17RE mediates polyIC-induced exacerbation of experimental allergic asthma. Respir Res. 2020 Jul 8;21(1):176. [Content Brief]
[2]. Jasper F Nies, et al. IL-17C/IL-17RE: Emergence of a Unique Axis in TH17 Biology. Front Immunol. 2020 Feb 26;11:341. [Content Brief]
[3]. Xinyang Song, et al. IL-17RE is the functional receptor for IL-17C and mediates mucosal immunity to infection with intestinal pathogens. Nat Immunol. 2011 Oct 12;12(12):1151-8. [Content Brief]
[4]. Caini Liu, et al. The flavonoid cyanidin blocks binding of the cytokine interleukin-17A to the IL-17RA subunit to alleviate inflammation in vivo. Sci Signal. 2017 Feb 21;10(467):eaaf8823. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)