Biotinylated Human MSR1 / CD204 Protein, Avitag™,His Tag, active trimer (MALS verified)

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MS1-H82Q3-25ug
$360.00
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MS1-H82Q3-200ug
$1,565.00
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MS1-H82Q3
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Synonyms

MSR1, CD204, SCARA1, SR-A, phSR1, phSR2

Source

Biotinylated Human MSR1 Protein, Avitag,His Tag, active trimer (MS1-H82Q3) is expressed from human 293 cells (HEK293). It contains AA Lys 77 - Leu 451 (Accession # P21757).

Predicted N-terminus: Gly

Molecular Characterization

This protein carries an Avi tag (Avitag™) at the N-terminus, followed by a polyhistidine tag.

The protein has a calculated MW of 44.9 kDa. The protein migrates as 55-90 kDa when calibrated against Star Ribbon Pre-stained Protein Marker under reducing (R) condition (SDS-PAGE) due to glycosylation.

Labeling

Biotinylation of this product is performed using Avitag™ technology. Briefly, the single lysine residue in the Avitag is enzymatically labeled with biotin.

Protein Ratio

Passed as determined by the SABA assay / HABA assay / binding ELISA.

Purity

>95% as determined by SDS-PAGE.

>90% 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.

Introduction de fond

Macrophage scavenger receptor 1 (MSR1), also known as scavenger receptor-A (SR-A) or cluster of differentiation 204 (CD204). Present primarily on the surface of various types of macrophage, This receptor is macrophage-specific trimeric integral membrane glycoproteins and have been implicated in many macrophage-associated physiological and pathological processes such as atherosclerosis, innate and adaptive immunity, lung and liver disease, and more recently, cancer.