IFN-alpha 1, human recombinant protein Reference: P1058-.1 IFN-alpha 1, expressed in E. coli, suitable for cell culture.
IFN-alpha 1, human recombinant protein Reference: P1058-1 IFN-alpha 1, expressed in E. coli, suitable for cell culture.
SHANK3 blocking peptide Reference: GTX31480-PEP This gene is a member of the Shank gene family. Shank proteins are multidomain scaffold proteins of the postsynaptic density that connect neurotransmitter receptors, ion channels, and other membrane proteins to the actin cytoskeleton and G-protein-coupled signaling pathways. Shank proteins also play a role in synapse formation and dendritic spine maturation. Mutations in this gene are a cause of autism spectrum disorder (ASD), which is characterized by impairments in social interaction and communication, and restricted behavioral patterns and interests. Mutations in this gene also cause schizophrenia type 15, and are a major causative factor in the neurological symptoms of 22q13.3 deletion syndrome, which is also known as Phelan-McDermid syndrome. Additional isoforms have been described for this gene but they have not yet been experimentally verified. [provided by RefSeq, Mar 212]
VEGF-C, human recombinant protein Reference: P1059-.01 VEGF-C, expressed in E. coli, suitable for cell culture.
THBS4 blocking peptide Reference: GTX31481-PEP The protein encoded by this gene belongs to the thrombospondin protein family. Thrombospondin family members are adhesive glycoproteins that mediate cell-to-cell and cell-to-matrix interactions. This protein forms a pentamer and can bind to heparin and calcium. Studies of the rat counterpart suggest that this protein may be involved in local signaling in the developing and adult nervous system. [provided by RefSeq, Jul 28]
VEGF-C, human recombinant protein Reference: P1059-.05 VEGF-C, expressed in E. coli, suitable for cell culture.
VEGF-C, human recombinant protein Reference: P1059-1 VEGF-C, expressed in E. coli, suitable for cell culture.
SEPT1 blocking peptide Reference: GTX31484-PEP This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis and the maintenance of cellular morphology. This gene encodes a protein that can form homo- and heterooligomeric filaments, and may contribute to the formation of neurofibrillary tangles in Alzheimer's disease. Alternatively spliced transcript variants have been found but the full-length nature of these variants has not been determined. [provided by RefSeq, Dec 212]
IL-17A, Mouse Recombinant Reference: P1060-.01 Proinflammatory cytokine produced by activated T cells.
BMP15 blocking peptide Reference: GTX31485-PEP The protein encoded by this gene is a member of the bone morphogenetic protein family which is part of the transforming growth factor-beta superfamily. The transforming growth factor-beta superfamily includes large families of growth and differentiation factors. It is thought that this protein may be involved in oocyte maturation and follicular development as a homodimer or by forming heterodimers with a related protein, Gdf9. Defects in this gene are the cause of ovarian dysgenesis 2.[provided by RefSeq, Sep 29]