- EGFR Signaling Pathway
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- p53 Pathway
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- Cytokine Signaling
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Chemokine (C-C motif) ligand 3 Protein Datasheet
CCL3 / Mip1a Protein Price Inquiry ( Available Sizes )
CCL3 / Mip1a Protein Product Information
|Synonym :||CCL3, Mip1a, Scya3|
A DNA sequence encoding the mouse CCL3 (P10855) (Ala24-Ala92) was expressed and purified.
CCL3 / Mip1a Protein QC Testing
|Purity:||> 95 % as determined by SDS-PAGE||SDS-PAGE:
CCL3 / Mip1a protein
|Endotoxin:||Please contact us for more information.|
|Stability:||Samples are stable for up to twelve months from date of receipt at -70℃|
|Predicted N terminal:||Met|
The recombinant mouse CCL3consists of 70 amino acids and predicts a molecular mass of 8.01 KDa. It migrates as an approximately 8-14 KDa band in SDS-PAGE under reducing conditions.
|Formulation:||Lyophilized from sterile 30% acetonitrile 0.1%TFA.
CCL3 / Mip1a Protein Usage Guide
|Storage:||Store it under sterile conditions at -70℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.|
|Reconstitution:||A hardcopy of COA with reconstitution instruction is sent along with the products. Please refer to it for detailed information.|
CCL3 / Mip1a Protein Related Products & Topics
CCL3 / Mip1a Protein Description
CCL3 is a cytokine. It is a member of the CC chemokine family. Chemokines are a family of structurally related leukocyte chemoattractant cytokines that play a central role during immunoregulatory and inflammation processes. All chemokines contain four conserved cysteines linked by disulfide bonds, and two major subfamilies, namely CXC and CC, are defined on the basis of the first two cysteines which are separated by one amino acid or are adjacent. CCL3 plays a role in the acute inflammatory state in the recruitment and activation of polymorphonuclear leukocytes.
- Zhao RY. et al., 2005, Cell Res. 15 (3): 143-9.
- Joseph AM. et al., 2005, Curr HIV Res. 3 (1): 87-94.
- Muthumani K. et al., 2004, DNA Cell Biol. 23 (4): 239-47.