SHH Polyclonal Antibody
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: SHH
Target Synonym: HHG 1;HHG-1;HHG1;HLP 3;HLP3;Holoprosencephaly 3;HPE 3;HPE3;MCOPCB5;shh;SHH;SMMC I;SMMCI;Sonic Hedgehog (Drosophila) homolog;sonic hedgehog homolog (Drosophila);Sonic hedgehog homolog;Sonic hedgehog protein;Sonic hedgehog protein C-product;TPT;TPTPS
Research Areas: Cancer;Epigenetics and Nuclear Signaling;Metabolism;Developmental Biology;Stem Cells
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse;Rat
Application: IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: Q15465
Accession:
Background: 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.
Concentration: 0.8 mg/mL
Immunogen: Synthetic peptide of human SHH
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: IHC 1:50-1:100
Calculated MW:
ObservedMW:
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SHH Polyclonal Antibody
SHH Polyclonal Antibody
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: SHH
Target Synonym: HHG 1;HHG-1;HHG1;HLP 3;HLP3;Holoprosencephaly 3;HPE 3;HPE3;MCOPCB5;shh;SHH;SMMC I;SMMCI;Sonic Hedgehog (Drosophila) homolog;sonic hedgehog homolog (Drosophila);Sonic hedgehog homolog;Sonic hedgehog protein;Sonic hedgehog protein C-product;TPT;TPTPS
Research Areas: Cancer;Epigenetics and Nuclear Signaling;Metabolism;Developmental Biology;Stem Cells
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse;Rat
Application: IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: Q15465
Accession:
Background: 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.
Concentration: 0.8 mg/mL
Immunogen: Synthetic peptide of human SHH
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: IHC 1:50-1:100
Calculated MW:
ObservedMW:
Original: $358.65
-70%$358.65
$107.59Product Information
Product Information
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Description
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: SHH
Target Synonym: HHG 1;HHG-1;HHG1;HLP 3;HLP3;Holoprosencephaly 3;HPE 3;HPE3;MCOPCB5;shh;SHH;SMMC I;SMMCI;Sonic Hedgehog (Drosophila) homolog;sonic hedgehog homolog (Drosophila);Sonic hedgehog homolog;Sonic hedgehog protein;Sonic hedgehog protein C-product;TPT;TPTPS
Research Areas: Cancer;Epigenetics and Nuclear Signaling;Metabolism;Developmental Biology;Stem Cells
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse;Rat
Application: IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: Q15465
Accession:
Background: 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.
Concentration: 0.8 mg/mL
Immunogen: Synthetic peptide of human SHH
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: IHC 1:50-1:100
Calculated MW:
ObservedMW:
