Recombinant Human SF20/MYDGF Protein, CF

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2 μg/lane of Recombinant Human SF20/MYDGF (Catalog # 10231-MY) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® Blue staining, showing bands at 14-15 ...read more
When Recombinant Human SF20/MYDGF (Catalog # 10231-MY) is immobilized at 2 μg/mL, 100 μg/well, Recombinant Human Protein Disulfide Isomerase/P4HB (Catalog # 4236-DI) binds with an ED50 of 0.8‑4.8 μg/mL.

Product Details

Summary
Reactivity HuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

Order Details

Recombinant Human SF20/MYDGF Protein, CF Summary

Details of Functionality
Measured by its binding ability in a functional ELISA. When Recombinant Human SF20/MYDGF (Catalog # 10231-MY) is immobilized at 2 μg/mL (100 μL/well), Recombinant Human Protein Disulfide Isomerase/P4HB (Catalog # 4236-DI) binds with an ED50 of 0.8-4.8 μg/mL.
Source
Chinese Hamster Ovary cell line, CHO-derived human SF20/MYDGF protein
Val32-Leu173
Accession #
N-terminal Sequence
Val32
Protein/Peptide Type
Recombinant Proteins
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Endotoxin Note
<0.10 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Theoretical MW
16 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
14-15 kDa, under reducing conditions

Packaging, Storage & Formulations

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.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose.
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 500 μg/mL in PBS.

Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for Recombinant Human SF20/MYDGF Protein, CF

  • C19orf10
  • chromosome 19 open reading frame 10
  • EUROIMAGE1875335
  • IL25
  • IL27
  • IL27w
  • interleukin 27 working designation
  • Interleukin-25
  • Ly6elg
  • MYDGF
  • myeloid-derived growth factor
  • R33729_1
  • SF20
  • Stromal cell-derived growth factor SF20
  • UPF0556 protein C19orf10

Background

Myeloid-Derived Growth Factor, or MYDGF, is a Bone marrow-derived monocyte protein, and it is correlated with enhanced metabolic activity, suppression of apoptosis, and stimulation of cell proliferation (1). MYDGF is expressed predominantly in inflammatory cells, such as monocytes and macrophages (1). Up-regulation of MYDGF expression was also found during adipocyte differentiation (2). Expression of MYDGF was induced in the circulation and heart tissue after myocardial infarction. It promotes cardiac myocyte survival by stimulating endothelial cell proliferation through a MAPK1/3-, STAT3- and CCND1-mediated signaling pathway, and inhibits cardiac myocyte apoptosis in a PI3K/AKT-dependent signaling pathway (1). MYDGF was found over-expressed in approximately two-thirds of Hepatocellular Carcinoma (HCC) tissues, and its expression was significantly positively correlated with that of alpha-fetoprotein (AFP) (3). In HCC, MYDGF could regulate cell proliferation through activating Akt/mitogen-activated protein kinase pathways (3). Human MYDGF shares 92% and 85% amino acid sequence identity to mouse and rat MYDGF, respectively. Intriguingly, virtually all homologs of MYDGF have a C-terminal putative ER retention sequence BXEL (B: Arg, His, or Lys; X: variable residue; E: Glu; L: Leu), which has the potential to retain human MYDGF and its homologs in the ER, whereas truncated MYDGF without BXEL is secreted from the cell (4). However, the functions of these different forms remain unclear.
  1. Korf-Klingebiel, M. et al. (2015) Nat. Med. 10:3778.
  2. Wang, P. et al. (2004) Cell. Mol. Life Sci. 61:2405
  3. Sunagozaka, H. et al. (2011) Int. J. Cancer 129:1576
  4. Bortnov, V. et al. (2018) J. Biol. Chem. 293:13166.

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