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Recombinant Human IL-17 RC Protein, CF 50 UG

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產(chǎn)品介紹

    基本參數(shù)

    詳細(xì)說(shuō)明

    • Purity

      >95%, by SDS-PAGE under reducing conditions and visualized by silver stain.

    • Endotoxin Level

      <0.10 EU per 1 μg of the protein by the LAL method.  

    • Activity

      Measured by its ability to bind rhIL-17 in a functional ELISA with an estimated K    D < 20 nM.

    • Source

      Mouse myeloma cell line, NS0-derived Leu21-Ala454, with a C-terminal 6-His tag

    • Accession #

    • N-terminal Sequence    
      Analysis

      Leu21

    • Predicted Molecular Mass

      49 kDa

    • SDS-PAGE

      75-85 kDa, reducing conditions

    2269-IL

     

    Formulation Lyophilized from a 0.2 μm filtered solution in PBS and EDTA.


    Reconstitution Reconstitute at 200 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.      

    • 12 months from date of receipt, -20 to -70 °C as supplied.

    • 1 month, 2 to 8 °C under sterile conditions after reconstitution.

    • 3 months, -20 to -70 °C under sterile conditions after reconstitution.


    Background: IL-17 RC

    IL-17 receptor C (IL-17 RC; also known as IL-17 RL and IL-17 Rhom) is an 85 - 110 kDa member of the IL-17 receptor family. This is one of five families that currently comprise the cytokine receptor superfamily (1, 2, 3, 4, 5, 6). At this time, there are five members within the IL-17 receptor family, and these are termed IL-17 RA, B, C, D and E. Not all receptors appear to bind known members of the IL-17 cytokine family. To date, IL-17 RA is reported to bind IL-17(A), while IL-17 RB is reported to bind IL-17B and IL-17E (2, 4). Human IL-17 RC is a type I transmembrane glycoprotein that is expressed on a variety of nonhematopoietic cell types. These include endothelial cells (6, 7), chondrocytes and osteoblasts (8), breast and prostatic epithelium (6), and fibroblasts, plus renal tubular epithelium and skeletal muscle cells (8, 9). Full-length IL-17 RC is synthesized as a 791 amino acid (aa) precursor (10, 11). It contains a 20 aa signal sequence, a 518 aa extracellular domain (ECD) (aa 21 - 538), a 21 aa transmembrane segment, and a 232 aa cytoplasmic region. Although IL-17 RA has two fibrinogen-like regions in its ECD that contribute to its function, no such architecture has been identified in the ECD of IL-17 RC (12). Based on studies looking at exon deletions, a key ligand-binding site would appear to exist over aa 425 - 441 (13). The gene for human IL-17 RC contains 19 exons. It is estimated that there are over 90 alternative splice forms, with transmembrane-containing isoforms predominating (6, 14). The full-length isoform is estimated to occur approximately 10% of the time, while the three most common isoforms, as a group, occur about 50% of the time. Based on limited information, alternative splicing appears to regulate ligand specificity (13). R&D Systems IL-17 RC corresponds to IL-17 RC isoform # 3, which shows deletions of aa 36 - 106 and 264 - 278 relative to the full-length form (10). Over the ECD, IL-17 RC isoform #3 is 68% aa identical to mouse IL-17 RC ECD. IL-17 RC is the cognate receptor for IL-17F, and binds IL-17A with similar affinity (13). With IL-17 RA, it forms a definitive receptor for both IL-17A and IL-17F. The stoichiometry is unclear; it may form a heterodimer with IL-17 RA, or a heterotrimer with a preexisting IL-17 RA homodimer (4, 9, 13, 15). The heteromeric nature of the receptor may be important given that the predominant form of the IL-17 cytokine is now considered to be an IL-17A:IL-17F heterodimer (4).

    • References:

      1. Gaffen, S.L. et al. (2006) Vitam. Horm. 74:255.

      2. Weaver, C.T. et al. (2007) Annu. Rev. Immunol. 25:821.

      3. Moseley, T.A. et al. (2003) Cytokine Growth Factor Rev. 14:155.

      4. Shen, F. and S.L. Gaffen (2008) Cytokine 41:92.

      5. You, Z. et al. (2006) Cancer Res. 66:175.

      6. You, Z. et al. (2007) Neoplasia 9:464.

      7. Gerritsen, M.E. et al. (2003) Br. J. Pharmacol. 140:595.

      8. Kokubu, T. et. Al. (2008) J. Hictochem. Cytochem. 56:89.

      9. Toy, D. et al. (2006) J. Immunol. 177:36.

      10. GenBank Accession # Q96F46.

      11. Haudenschild, D. et al. (2002) J. Biol. Chem. 277:4309.

      12. Kramer, J.M. et al. (2007) J. Immunol. 179:6379.

      13. Kuestner, R.E. et al. (2007) J. Immunol. 179:5462.

      14. Haudenschild, D.R. et al. (2006) Prostate 66:1268.

      15. Kramer, J.M. et al. (2006) J. Immunol. 176:711.

    • Long Name:

      Interleukin 17 Receptor C, Transcript Variant 3

    • Entrez Gene IDs:

      84818 (Human); 171095 (Mouse)

    • Alternate Names:

      FLJ95963; FLJ96005; IL-17 RC; IL-17 receptor C; IL-17 RL; IL17F receptor; IL17RC; IL-17RC; IL17Rhom; IL17RL; IL-17RL; IL17-RL; interleukin 17 receptor C; interleukin-17 receptor C; Interleukin-17 receptor homolog; Interleukin-17 receptor-like protein; MGC10763; zcytoR14



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