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CCL23 Protein (AA 46-120)

Cette protéine Recombinant CCL23 est exprimée dans Escherichia coli (E. coli).
N° du produit ABIN2666897

Aperçu rapide pour CCL23 Protein (AA 46-120) (ABIN2666897)

Antigène

Voir toutes CCL23 Protéines
CCL23 (Chemokine (C-C Motif) Ligand 23 (CCL23))

Type de proteíne

Recombinant

Activité biologique

Active

Origine

  • 10
  • 1
  • 1
Humain

Source

  • 8
  • 1
  • 1
  • 1
Escherichia coli (E. coli)

Application

Flow Cytometry (FACS)

Pureté

> 98 % , as determined by Coomassie stained SDS-PAGE.
  • Attributs du protein

    AA 46-120

    Stérilité

    0.22 μm filtered

    niveau d'endotoxine

    Less than 0.01 ng per μg cytokine as determined by the LAL method.

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  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Commentaires

    Biological activity: Bioactivity was measured by its property to chemoattract THP-1 cells in a dose dependent manner.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Reconstitution

    For maximum results, quick spin vial prior to opening. Stock solutions should be prepared at no less than 10 μg/mL in sterile buffer (PBS, HPBS, DPBS, and EBSS) containing carrier protein such as 1 % BSA or HSA. After dilution, the cytokine can be stored between 2 °C and 8 °C for one month or from -20 °C to -70 °C for up to 3 months.

    Buffer

    0.22 μm filtered protein solution is in PBS.

    Conseil sur la manipulation

    Avoid repeated freeze/thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    Unopened vial can be stored between 2°C and 8°C for three months, at -20°C for six months, or at -70°C for one year.
  • Antigène

    CCL23 (Chemokine (C-C Motif) Ligand 23 (CCL23))

    Autre désignation

    CCL23

    Sujet

    Human CCL23 was initially identified in a cDNA library derived from human endothelial cells. CCL23 has six cysteine residues and posseses a separately encoded amino-terminal domain, characteristic of similar chemokines CCL6, CCL9, and CCL15. These four chemokines are weak agonists for CCR1, nevertheless, they can be proteolytically cleaved in the amino-terminus, resulting in forms with higher chemoattractant activity. Thus, NH2-terminus truncated forms of CCL23 have been detected in synovial fluid of patients with rheumatoid arthritis (RA). In vitro studies have shown that CCL23 can be processed by MMPs at the amino and carboxyl terminus. CCL23 (26-99) is the predominant stable form after using MMP1, 2, 3, 7, 8, or 12. CCL23 (30-99) is formed by MMP14, elastase, and proteolytic activity in arthritic synovial fluid. In addition, CCL23 has been detected in serum of patients with active RA, in conjunction with CXCL13, TNFSR9, M-CSF, and TNFα. High levels in serum of these cytokines correlate with joint inflammation and have been considered as biomarkers of active RA. Also, high levels of CCL23 have been detected in plasma of atherosclerotic patients. High expression of CCL23 has been found in skin of atopic dermatitis patients, and in mucosal epithelial cells and inflammatory cells in sinonasal tissues of patients with chronic rhinosinusitis (CRS).

    Poids moléculaire

    The 75 amino acid recombinant protein has a predicted molecular mass of approximately 8.5 kDa. The DTT-reduced and non-reduced protein migrate at approximately 12 and 14 kDa by SDS-PAGE respectively. The N-terminal amino acid is Arg.
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