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CXCL4/PF4 Protein, Human

CXCL4/PF4 Protein, Human

Catalog Number: UA040566 Brand: UA BIOSCIENCE
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Regular price $115 USD
Regular price Sale price $115 USD
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Product Details

Product Specification


Species Human
Synonyms Platelet factor 4, PF-4, C-X-C motif chemokine 4, Iroplact, Oncostatin-A
Accession P02776
Amino Acid Sequence

Glu 32-Ser101 with His Tag at the C-Terminus

Expression System Yeast
Molecular Weight

12-13 kDa (Reducing)

Purity >95% by SDS-PAGE and HPLC.
Endotoxin <0.1EU/μg
Conjugation Unconjugated
Tag His Tag
Physical Appearance Lyophilized Powder
Storage Buffer

20mM Sodium Citrate, 150mM NaCl, 5% Trehalose, pH5.0

Reconstitution

Reconstitute at 0.1-1 mg/ml according to the size in ultrapure water after rapid centrifugation.

Stability & Storage

·12 months from date of receipt, lyophilized powder stored at -20 to -80℃.
·3 months, -20 to -80℃ under sterile conditions after reconstitution.
·1 week, 2 to 8℃ under sterile conditions after reconstitution.
·Please avoid repeated freeze-thaw cycles.

Reference

Nat Commun. 2023 Aug 16;14(1):4375.
Cytokine Growth Factor Rev. 2011 Feb;22(1):1-18.

Background

CXCL4, also known as Platelet Factor 4 (PF4), is a member of the C-X-C chemokine family and was the first chemokine to be identified. The human PF4 gene encodes a small protein of approximately 7.8 kDa comprising 70 amino acids in its mature form. CXCL4 is predominantly localized within the alpha granules of platelets, with a remarkably high concentration of approximately 20 μg of PF4 present in every 1×10⁹ platelet cells. In plasma, PF4 is found at a concentration of approximately 2–10 ng/mL.

CXCL4 exerts pleiotropic biological functions. It is recognized as a potent antiangiogenic chemokine that inhibits endothelial cell proliferation and migration, leading to suppression of angiogenesis. The angiostatic activity of CXCL4 involves multiple mechanisms, including interference with angiogenic growth factors such as bFGF-2 and VEGF165, activation of the CXCR3B receptor (a splice variant of CXCR3), interactions with integrins, and interference with cell cycle progression.

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Bioactivity

Determined by its ability to chemoattract THP-1 using a concentration range of 0.01-10.0 ng/ml.

SDS-PAGE

2μg (R: reducing condition, N: non-reducing condition).

RP-HPLC

>95% as determined by RP-HPLC.