B7-1/CD80 Long Isoform Extracellular Domain (human, recombinant, His-tagged) Reference: 32013-100 Source: Recombinant human C-terminal His-tagged CD80 expressed in HEK293 cells • Amino acids: 35-242 • MW: 25.4 kDa
ATG4A blocking peptide Reference: GTX31941-PEP Autophagy is the process by which endogenous proteins and damaged organelles are destroyed intracellularly. Autophagy is postulated to be essential for cell homeostasis and cell remodeling during differentiation, metamorphosis, non-apoptotic cell death, and aging. Reduced levels of autophagy have been described in some malignant tumors, and a role for autophagy in controlling the unregulated cell growth linked to cancer has been proposed. This gene encodes a member of the autophagin protein family. The encoded protein is also designated as a member of the C-54 family of cysteine proteases. Transcript variants that encode distinct isoforms have been identified. [provided by RefSeq, Jul 28]
B7-1/CD80 Long Isoform Extracellular Domain (human, recombinant, His-tagged) Reference: 32013-200 Source: Recombinant human C-terminal His-tagged CD80 expressed in HEK293 cells • Amino acids: 35-242 • MW: 25.4 kDa
ATG4B blocking peptide Reference: GTX31942-PEP Autophagy is the process by which endogenous proteins and damaged organelles are destroyed intracellularly. Autophagy is postulated to be essential for cell homeostasis and cell remodeling during differentiation, metamorphosis, non-apoptotic cell death, and aging. Reduced levels of autophagy have been described in some malignant tumors, and a role for autophagy in controlling the unregulated cell growth linked to cancer has been proposed. This gene encodes a member of the autophagin protein family. The encoded protein is also designated as a member of the C-54 family of cysteine proteases. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 28]
CD28 Long Isoform Extracellular Domain (human, recombinant) Reference: 32014-100 Source: Recombinant C-terminal human IgG1 Fc-tagged CD28 expressed in HEK293 cells • Amino acids: 19-152 • MW: 42 kDa
JAK2 blocking peptide Reference: GTX31943-PEP This gene product is a protein tyrosine kinase involved in a specific subset of cytokine receptor signaling pathways. It has been found to be constituitively associated with the prolactin receptor and is required for responses to gamma interferon. Mice that do not express an active protein for this gene exhibit embryonic lethality associated with the absence of definitive erythropoiesis. [provided by RefSeq, Jul 28]
CD28 Long Isoform Extracellular Domain (human, recombinant) Reference: 32014-200 Source: Recombinant C-terminal human IgG1 Fc-tagged CD28 expressed in HEK293 cells • Amino acids: 19-152 • MW: 42 kDa
CTHRC1 blocking peptide Reference: GTX31944-PEP This locus encodes a protein that may play a role in the cellular response to arterial injury through involvement in vascular remodeling. Mutations at this locus have been associated with Barrett esophagus and esophageal adenocarcinoma. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 212]
CD1b Long Isoform Extracellular Ligand-binding Domain (human, recombinant) Reference: 32015-100 Source: Recombinant C-terminal human IgG1 Fc-His-tagged CD1b expressed in HEK293 cells • Amino acids: 18-303 • MW: 58.6 kDa
Adenosine A2b Receptor blocking peptide Reference: GTX31945-PEP This gene encodes an adenosine receptor that is a member of the G protein-coupled receptor superfamily. This integral membrane protein stimulates adenylate cyclase activity in the presence of adenosine. This protein also interacts with netrin-1, which is involved in axon elongation. The gene is located near the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 28]
CD1b Long Isoform Extracellular Ligand-binding Domain (human, recombinant) Reference: 32015-50 Source: Recombinant C-terminal human IgG1 Fc-His-tagged CD1b expressed in HEK293 cells • Amino acids: 18-303 • MW: 58.6 kDa
SLC29A1 blocking peptide Reference: GTX31946-PEP This gene is a member of the equilibrative nucleoside transporter family. The gene encodes a transmembrane glycoprotein that localizes to the plasma and mitochondrial membranes and mediates the cellular uptake of nucleosides from the surrounding medium. The protein is categorized as an equilibrative (as opposed to concentrative) transporter that is sensitive to inhibition by nitrobenzylthioinosine (NBMPR). Nucleoside transporters are required for nucleotide synthesis in cells that lack de novo nucleoside synthesis pathways, and are also necessary for the uptake of cytotoxic nucleosides used for cancer and viral chemotherapies. Multiple alternatively spliced variants, encoding the same protein, have been found for this gene. [provided by RefSeq, Jul 28]