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Recombinant Human OLFM4 Protein (His Tag)

  • Cat.No.:PKSH033360

  • Expression host: HEK293 Cells

To Purchase PKSH033360

Size:
  • 10μg
  • 50μg
Price: $178
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Description

Synonyms Olfactomedin-4;OLM4;Antiapoptotic protein GW112;G-CSF-stimulated clone 1 protein;hGC-1;hOLfD;OLFM4;GW112
Species Human
Expression_host HEK293 Cells
Sequence Asp21-Gln510
Accession Q6UX06
Mol_Mass 56.9 kDa
AP_Mol_Mass 60-90 kDa
Tag C-His

Properties

Purity > 80 % as determined by reducing SDS-PAGE.
Endotoxin level < 1.0 EU per μg of the protein as determined by the LAL method.
Storage Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months.
Shipping This product is provided as lyophilized powder which is shipped with ice packs.
Formulation Lyophilized from a 0.2 μm filtered solution of PBS, 5%Trehalose, PH7.4.
Normally 5 % - 8 % trehalose, mannitol and 0.01% Tween80 are added as protectants before lyophilization.
Please refer to the specific buffer information in the printed manual.
Reconstitution Please refer to the printed manual for detailed information.

Background

Olfactomedin-4/OLFM4 is a secreted protein which contains one olfactomedin-like domain. OLFM4 is expressed during myeloid lineage development;it strongly expressed in the prostate;small intestine;colon and moderately expressed in the bone marrow and stomach. OLFM4 is an antiapoptotic factor that promotes tumor growth. It expressed at high levels in stomach cancer and colon cancer tissues. it promotes proliferation of pancreatic cancer cells by favoring the transition from the S to G2/M phase. In myeloid leukemic cell lines; OLFM4 inhibits cell growth and induces cell differentiation and apoptosis. Through interaction with cell surface lectins and cadherin; OLFM4 facilitates cell adhesion. It may play a role in the inhibition of EIF4EBP1 phosphorylation/deactivation. Induction of OLFM4 in cancer cells was reported to have a novel antiapoptotic action via binding to the potent apoptosis inducer GRIM-19.

Citations

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