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In vitro transcription of capped mRNA with modified nucleotides and Poly(A) tail
TSA (Tyramide Signal Amplification), used for signal amplification of ISH, IHC and IC etc.
Separation of phosphorylated and non-phosphorylated proteins without phospho-specific antibody
A convenient and sensitive way for cell proliferation assay and cytotoxicity assay
Protect the integrity of proteins from multiple proteases and phosphatases for different applications.
Macrophage inflammatory protein-3 β (MIP-3β) is a CC chemokine produced in the thymus, lymph nodes and activated bone marrow stromal cells. MIP-3β signals through the chemokine receptor CCR-7/EBI-1/BLR-2. MIP-3β is a chemoattractant for T and B lymphocytes, and myeloid progenitor cells. The expression of MIP-3β is down-regulated by the anti-inflammatory cytokine IL-10. CCL19 and CCL21 control survival, apoptosis, migratory speed, and maturation of dendritic cells, rate of endocytosis and the cytoarchitecture.
The murine MIP-3β cDNA encodes a 108 aa protein contains a 25 aa signal sequence. Human MIP-3β is active on murine cells. Recombinant murine MIP-3β is a 9.2 kDa protein containing 83 amino acid residues.
