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CD25 Protein (C-Term, Extracellular Domain)

This Recombinant CD25 protein is produced in HEK-293T Cells.
Catalog No. ABIN1684666

Quick Overview for CD25 Protein (C-Term, Extracellular Domain) (ABIN1684666)

Target

See all CD25 (IL2RA) Proteins
CD25 (IL2RA) (Interleukin 2 Receptor, alpha (IL2RA))

Protein Type

Recombinant

Origin

  • 18
  • 8
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Mouse

Source

  • 14
  • 9
  • 8
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
HEK-293T Cells

Purity

> 97 %, as determined by SDS-PAGE and HPLC
  • Protein Characteristics

    C-Term, Extracellular Domain

    Specificity

    Optimized DNA sequence encoding extracellular domain of mouse CD25 including a C-terminal polyHis tag was expressed in HEK293 cells.

    Characteristics

    Recombinant mouse CD25 is a monomer protein consisting of23 amino acid residue subunits, due to glycosylation migrates as an approximately 50 kDa protein on SDS-PAGE.

    Sterility

    0.2 μm filtered

    Endotoxin Level

    Endotoxin content was assayed using a LAL gel clot method. Endotoxin level was found to be less than 0.1 ng/µg(1EU/µg).
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  • Restrictions

    For Research Use only
  • Buffer

    PBS solution, pH7.2

    Handling Advice

    Avoid repeated freeze/thaw cycles.

    Storage

    -20 °C

    Storage Comment

    The lyophilized antibody is stable for at least 1 year from date of receipt at -20 °C. Upon reconstitution, this antibody can be stored in working aliquots at - 8 °C for one month, or at -20 °C for six months without detectable loss of activity.

    Expiry Date

    12 months
  • Target

    CD25 (IL2RA) (Interleukin 2 Receptor, alpha (IL2RA))

    Alternative Name

    CD25

    Background

    G-CSF is secreted by monocytes, macrophages, and neutrophils after cell activation. It is produced also by stromal cells, fibroblasts, and endothelial cells. Epithelial carcinomas, acute myeloid leukemia cells and various tumor cell lines. The synthesis of G-CSF can be induced by bacterial endotoxins, TNF, IL1 and GM-CSF. Comparison of the primary sequence of G-CSF with those of the two other colony stimulating factors, GM-CSF and M-CSF, shows that the three factors are not related to each other. Murine and human G-CSF show a sequence homology of approximately 70 % at the DNA level and of 72 % at the protein level. The G-CSF receptorCD114, is expressed on all cells of the neutrophils and granulocytes lineage. It is expressed also in placenta cells, endothelial cells and various carcinoma cell lines. Human G-CSF is active in murine cells and vice versa. G-CSF stimulates the proliferation and differentiation of hematopoietic progenitor cells committed to the neutrophils and granulocytes lineage in a dose-dependent manner.G-CSF synergises with some other cytokines, including GM-CSF and IL4. GM-CSF and G-CSF are required, for example, to develop neutrophilic colonies in vitro. The concerted action of G-CSF and Epo is required to support the growth of mixed colonies of the early erythroid progenitors. A combination of IL4 with G-CSF has been shown to lead to synergistic suppression of the growth of some human leukemic cell lines.

    UniProt

    P01590

    Pathways

    JAK-STAT Signaling, Growth Factor Binding, Activated T Cell Proliferation
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