MIP-3 beta (CCL19), mouse, Reference: D-65877 Recombinant Mouse Macrophage Inflammatory Protein 3-beta (CCL19)
SETMAR blocking peptide Reference: GTX23823-PEP This gene encodes a fusion protein that contains an N-terminal histone-lysine N-methyltransferase domain and a C-terminal mariner transposase domain. The encoded protein binds DNA and functions in DNA repair activities including non-homologous end joining and double strand break repair. The SET domain portion of this protein specifically methylates histone H3 lysines 4 and 36. This gene exists as a fusion gene only in anthropoid primates, other organisms lack mariner transposase domain. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 213]
PLGF-1, mouse, recombinant (Sf9) Reference: D-66021 Recombinant Mouse Placenta Growth Factor 1 (Sf9 cell-derived)
RNF3 (247 aa isoform) blocking peptide Reference: GTX23892-PEP The protein encoded by this gene contains a C3HC4 type RING finger, which is a motif known to be involved in protein-protein interactions. The specific function of this protein has not yet been determined. [provided by RefSeq, Jul 28]
PLGF-2, mouse, recombinant Reference: D-66022 Recombinant Mouse Placenta Growth Factor 2 (E. coli-derived)
NUMB blocking peptide Reference: GTX24147-PEP The protein encoded by this gene plays a role in the determination of cell fates during development. The encoded protein, whose degradation is induced in a proteasome-dependent manner by MDM2, is a membrane-bound protein that has been shown to associate with EPS15, LNX1, and NOTCH1. Four transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 28]
PLGF-2, mouse, recombinant Reference: D-66023 Recombinant Mouse Placenta Growth Factor 2 (insect cell-derived)
Park7 / DJ-1 blocking peptide Reference: GTX24150-PEP The product of this gene belongs to the peptidase C56 family of proteins. It acts as a positive regulator of androgen receptor-dependent transcription. It may also function as a redox-sensitive chaperone, as a sensor for oxidative stress, and it apparently protects neurons against oxidative stress and cell death. Defects in this gene are the cause of autosomal recessive early-onset Parkinson disease 7. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 28]
ALMS1 blocking peptide Reference: GTX24306-PEP This gene encodes a protein containing a large tandem-repeat domain. The mouse ortholog of this gene has been shown to function in ciliogenesis in inner medullary collecting duct cells. Mutations in this gene have been associated with Alstrom syndrome. Alternative splice variants have been described but their full length sequences have not been determined.[provided by RefSeq, Mar 29]