Cynomolgus CD164 Protein, Fc Tag (MALS verified)

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CD4-C5253-100ug
$380.00
In Stock - Order by 4 PM ET for overnight delivery on Nov. 13, 2026.
CD4-C5253-1mg (500ug X 2)
$2,850.00
In Stock - Order by 4 PM ET for overnight delivery on Nov. 13, 2026.
CD4-C5253
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Synonyms

CD164, MUC-24, Endolyn, MGC-24

Source

Cynomolgus CD164 Protein, Fc Tag (CD4-C5253) is expressed from human 293 cells (HEK293). It contains AA Glu 24 - Asp 163 (Accession # XP_005551610.1).

Predicted N-terminus: Glu24

Molecular Characterization

This protein carries a human IgG1 Fc tag at the C-terminus.

The protein has a calculated MW of 41.1 kDa. The protein migrates as 75-120 kDa when calibrated against Star Ribbon Pre-stained Protein Marker under reducing (R) condition (SDS-PAGE) due to glycosylation.

Endotoxin

Less than 0.1 EU per μg by the LAL method / rFC method.

Purity

>90% as determined by SDS-PAGE.

>95% as determined by SEC-MALS.

Formulation

Lyophilized from 0.22 μm filtered solution in PBS, pH7.4 with trehalose as protectant.

Contact us for customized product form or formulation.

Reconstitution

Please see Certificate of Analysis for specific instructions.

For best performance, we strongly recommend you to follow the reconstitution protocol provided in the CoA.

Shipping and Storage

This product is shipped at ambient temperature.

For long term storage, the product should be stored at lyophilized state at -20°C or lower.

Please avoid repeated freeze-thaw cycles.

This product is stable after storage at:
  • -20°C to -70°C for 12 months in lyophilized state;
  • -70°C for 3 months under sterile conditions after reconstitution.

배경 소개

This gene encodes a transmembrane sialomucin and cell adhesion molecule that regulates the proliferation, adhesion and migration of hematopoietic progenitor cells. The encoded protein also interacts with the C-X-C chemokine receptor type 4 and may regulate muscle development. Elevated expression of this gene has been observed in human patients with Sezary syndrome, a type of blood cancer, and a mutation in this gene may be associated with impaired hearing. [provided by RefSeq, Oct 2016]

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