SPRED1 is a member of the Sprouty family of proteins and is phosphorylated by tyrosine kinase in response to several growth factors. The encoded protein can act as a homodimer or as a heterodimer with SPRED2 to regulate activation of the MAP kinase cascade. Defects in this gene are a cause of neurofibromatosis type 1-like syndrome (NFLS).
Overexpression of Spred1 inhibited NGF-induced neurite differentiation in rat PC12 cells, and both the EVH1 and SPRY domains were essential for the suppression.mouse Spred1 coprecipitated with and was phosphorylated by a constitutively activated Kit mutant. The KBD was required for Kit binding, but suppression of growth factor-induced MAP kinase required the SPRY domain.
Organism species: Homo sapiens (Human)
CATALOG NO. | PRODUCT NAME | APPLICATIONS | |
Proteins | n/a | Recombinant Sprouty Related, EVH1 Domain Containing Protein 1 (SPRED1) | Recombinant Protein Customized Service Offer |
Antibodies | n/a | Monoclonal Antibody to Sprouty Related, EVH1 Domain Containing Protein 1 (SPRED1) | Monoclonal Antibody Customized Service Offer |
n/a | Polyclonal Antibody to Sprouty Related, EVH1 Domain Containing Protein 1 (SPRED1) | Polyclonal Antibody Customized Service Offer | |
Assay Kits | n/a | CLIA Kit for Sprouty Related, EVH1 Domain Containing Protein 1 (SPRED1) | CLIA Kit Customized Service Offer |
n/a | ELISA Kit for Sprouty Related, EVH1 Domain Containing Protein 1 (SPRED1) | ELISA Kit Customized Service Offer |
Organism species: Mus musculus (Mouse)
CATALOG NO. | PRODUCT NAME | APPLICATIONS | |
Proteins | n/a | Recombinant Sprouty Related, EVH1 Domain Containing Protein 1 (SPRED1) | Recombinant Protein Customized Service Offer |
Antibodies | n/a | Monoclonal Antibody to Sprouty Related, EVH1 Domain Containing Protein 1 (SPRED1) | Monoclonal Antibody Customized Service Offer |
n/a | Polyclonal Antibody to Sprouty Related, EVH1 Domain Containing Protein 1 (SPRED1) | Polyclonal Antibody Customized Service Offer | |
Assay Kits | n/a | CLIA Kit for Sprouty Related, EVH1 Domain Containing Protein 1 (SPRED1) | CLIA Kit Customized Service Offer |
n/a | ELISA Kit for Sprouty Related, EVH1 Domain Containing Protein 1 (SPRED1) | ELISA Kit Customized Service Offer |
Organism species: Rattus norvegicus (Rat)
CATALOG NO. | PRODUCT NAME | APPLICATIONS | |
Proteins | n/a | Recombinant Sprouty Related, EVH1 Domain Containing Protein 1 (SPRED1) | Recombinant Protein Customized Service Offer |
Antibodies | n/a | Monoclonal Antibody to Sprouty Related, EVH1 Domain Containing Protein 1 (SPRED1) | Monoclonal Antibody Customized Service Offer |
n/a | Polyclonal Antibody to Sprouty Related, EVH1 Domain Containing Protein 1 (SPRED1) | Polyclonal Antibody Customized Service Offer | |
Assay Kits | n/a | CLIA Kit for Sprouty Related, EVH1 Domain Containing Protein 1 (SPRED1) | CLIA Kit Customized Service Offer |
n/a | ELISA Kit for Sprouty Related, EVH1 Domain Containing Protein 1 (SPRED1) | ELISA Kit Customized Service Offer |
- "Distinct requirements for the Sprouty domain for functional activity of Spred proteins."Biochem. J. 388:445-454(2005) [PubMed] [Europe PMC] [Abstract]
- "Complete sequencing and characterization of 21,243 full-length human cDNAs." Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
- "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
- "Expression and subcellular localization of Spred proteins in mouse and human tissues."Histochem. Cell Biol. 122:527-538(2004) [PubMed] [Europe PMC] [Abstract]
- "The Sprouty-related protein, Spred-1, localizes in a lipid raft/caveola and inhibits ERK activation in collaboration with caveolin-1."Genes Cells 10:887-895(2005) [PubMed] [Europe PMC] [Abstract]
- "Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype."Nat. Genet. 39:1120-1126(2007) [PubMed] [Europe PMC] [Abstract]
- "N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB."Proc. Natl. Acad. Sci. U.S.A. 109:12449-12454(2012) [PubMed] [Europe PMC] [Abstract]
- "SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype."J. Med. Genet. 46:431-437(2009) [PubMed] [Europe PMC] [Abstract]
- "Novel human pathological mutations. Gene symbol: SPRED1. Disease: Legius syndrome."Hum. Genet. 127:112-112(2010) [PubMed] [Europe PMC] [Abstract]
- "Legius syndrome in fourteen families." Hum. Mutat. 32:E1985-E1998(2011) [PubMed] [Europe PMC] [Abstract]