IRF2BP2 blocking peptide Reference: GTX32054-PEP This gene encodes an interferon regulatory factor-2 (IRF2) binding protein that interacts with the C-terminal transcriptional repression domain of IRF2. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 28]
VEGF-C (human, recombinant) Reference: 32054-50 Source: Recombinant human C-terminal His-tagged VEGF-C expressed in HEK293 cells • Amino acids: 103-227 • MW: 15.5 kDa
B9D1 blocking peptide Reference: GTX32055-PEP This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Three alternatively spliced transcript variants that encode different proteins have been described for this gene. [provided by RefSeq, Aug 211]
VEGF-D (human, recombinant) Reference: 32055-1 Source: Recombinant human C-terminal His-tagged VEGF-D expressed in HEK293 cells • Amino acids: 93-201 • MW: 13.6 kDa
VEGF-D (human, recombinant) Reference: 32055-10 Source: Recombinant human C-terminal His-tagged VEGF-D expressed in HEK293 cells • Amino acids: 93-201 • MW: 13.6 kDa
VEGF-D (human, recombinant) Reference: 32055-20 Source: Recombinant human C-terminal His-tagged VEGF-D expressed in HEK293 cells • Amino acids: 93-201 • MW: 13.6 kDa
FGF10 (human, recombinant) Reference: 32056-1 Source: Recombinant human FGF10 expressed in E. coli • Amino acids: 38-208 • MW: 19.6 kDa
Nkx2.6 blocking peptide Reference: GTX32059-PEP This gene encodes a homeobox-containing protein that belongs to the NK-2 homeobox family. This protein is a vertebrate homolog of Drosophila homeobox-containing protein called 'tinman', which has been shown to be essential for development of the heart-like dorsal vessel. In conjunction with related gene, NKX2-5, this gene may play a role in both pharyngeal and cardiac embryonic development. Mutations in this gene are associated with persistent truncus arteriosus.[provided by RefSeq, Aug 211]
FGF10 (human, recombinant) Reference: 32056-100 Source: Recombinant human FGF10 expressed in E. coli • Amino acids: 38-208 • MW: 19.6 kDa