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Anti-SHH Monoclonal Antibody (4U905)

(Synonyms: TPTPS, TPT, SMMCI, MCOPCB5, HPE3, HLP3, HHG1) Copy Product Info
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Synonyms: TPTPS, TPT, SMMCI, MCOPCB5, HPE3, HLP3, HHG1

Catalog No. TMAT-1335 Copy Product Info
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Anti-SHH Monoclonal Antibody (4U905) is a Mouse antibody targeting SHH. Anti-SHH Monoclonal Antibody (4U905) can be used in WB,IHC,FCM.

Anti-SHH Monoclonal Antibody
(4U905)

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Product Introduction

Bioactivity
Description
Anti-SHH Monoclonal Antibody (4U905) is a Mouse antibody targeting SHH. Anti-SHH Monoclonal Antibody (4U905) can be used in WB,IHC,FCM.
SynonymsTPTPS, TPT, SMMCI, MCOPCB5, HPE3, HLP3, HHG1
Ig Type
IgG1
Clone
4U905
Reactivity
Human,Mouse,Monkey
Application
Recommended Dose
WB: 1/500-1/2000; IHC: 1/200-1/1000; FCM: 1/200-1/400
Antibody Type
Monoclonal
Host SpeciesMouse
ConstructionHybridoma Monoclonal Antibody
PurificationPurified by protein A or protein G
AppearanceLiquid
FormulationPBS with 0.05% sodium azide
Concentration1 mg/mL
Research BackgroundThis 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. It is also thought that mutations in this gene or in its signalling pathway may be responsible for VACTERL syndrome, which is characterized by vertebral defects, anal atresia, tracheoesophageal fistula with esophageal atresia, radial and renal dysplasia, cardiac anomalies, and limb abnormalities. Additionally, mutations in a long range enhancer located approximately 1 megabase upstream of this gene disrupt limb patterning and can result in preaxial polydactyly.
Related Conjugates and Formulations
Conjucates
Unconjugated
Antigen Details
Immunogen
Purified recombinant fragment of human SHH (AA: 26-161) expressed in E. Coli.
Antigen Species
Human
Gene Name
SHH
Gene ID
Protein Name
Sonic hedgehog protein
Uniprot ID
Chemical Properties
Molecular WeightTheoretical: 49.6 kDa.
Stability & Storage
Stability & StorageStore at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles.
TransportShipping with blue ice.

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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
Related Tags: Anti-SHH Monoclonal Antibody (4U905) molecular weight