Descrizione Azione

This gene encodes a protein that is instrumental in patterning the early embryo. It has been implicated as the key inductive signal in patterning of the ventral neural tube, the anterior-posterior limb axis, and the ventral somites. Of three human proteins showing sequence and functional similarity to the sonic hedgehog protein of Drosophila, this protein is the most similar. The protein is made as a precursor that is autocatalytically cleaved; the N-terminal portion is soluble and contains the signalling activity while the C-terminal portion is involved in precursor processing. More importantly, the C-terminal product covalently attaches a cholesterol moiety to the N-terminal product, restricting the N-terminal product to the cell surface and preventing it from freely diffusing throughout the developing embryo. Defects in this protein or in its signalling pathway are a cause of holoprosencephaly (HPE), a disorder in which the developing forebrain fails to correctly separate into right and left hemispheres. HPE is manifested by facial deformities.

Codice: E-AB-15842_120μL Confezionamento: 120μL
Dettagli

This gene encodes a protein that is instrumental in patterning the early embryo. It has been implicated as the key inductive signal in patterning of the ventral neural tube, the anterior-posterior limb axis, and the ventral somites. Of three human proteins showing sequence and functional similarity to the sonic hedgehog protein of Drosophila, this protein is the most similar. The protein is made as a precursor that is autocatalytically cleaved; the N-terminal portion is soluble and contains the signalling activity while the C-terminal portion is involved in precursor processing. More importantly, the C-terminal product covalently attaches a cholesterol moiety to the N-terminal product, restricting the N-terminal product to the cell surface and preventing it from freely diffusing throughout the developing embryo. Defects in this protein or in its signalling pathway are a cause of holoprosencephaly (HPE), a disorder in which the developing forebrain fails to correctly separate into right and left hemispheres. HPE is manifested by facial deformities.

Codice: E-AB-15842_200μL Confezionamento: 200μL
Dettagli

This gene encodes a protein that is instrumental in patterning the early embryo. It has been implicated as the key inductive signal in patterning of the ventral neural tube, the anterior-posterior limb axis, and the ventral somites. Of three human proteins showing sequence and functional similarity to the sonic hedgehog protein of Drosophila, this protein is the most similar. The protein is made as a precursor that is autocatalytically cleaved; the N-terminal portion is soluble and contains the signalling activity while the C-terminal portion is involved in precursor processing. More importantly, the C-terminal product covalently attaches a cholesterol moiety to the N-terminal product, restricting the N-terminal product to the cell surface and preventing it from freely diffusing throughout the developing embryo. Defects in this protein or in its signalling pathway are a cause of holoprosencephaly (HPE), a disorder in which the developing forebrain fails to correctly separate into right and left hemispheres. HPE is manifested by facial deformities.

Codice: E-AB-15842_20μL Confezionamento: 20μL
Dettagli

A synthesized peptide derived from human SHIP1, corresponding to a region within the internal amino acids.

Codice: AF7926 Confezionamento: 50ul
Dettagli

A synthesized peptide derived from human SHIP1, corresponding to a region within C-terminal amino acids.

Codice: AF0252 Confezionamento: 100ul
Dettagli

A synthetic peptide from human SHIP1

Codice: BF4188
Dettagli
Codice: A60898-100 Confezionamento: 100 µl
Dettagli
Codice: A60898-020 Confezionamento: 20 µl
Dettagli
Codice: A60898-050 Confezionamento: 50 µl
Dettagli
Codice: A60898-020 Confezionamento: 20 µl
Dettagli
Codice: A60898-050 Confezionamento: 50 µl
Dettagli
Codice: A60898-100 Confezionamento: 100 µl
Dettagli