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Mouse Monoclonal Anti-Wnt3 antibody (STJ99296)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, ELISA
Recommended dilution: WB 1:500-2000; ELISA 1:10000-20000
Recommended protocols: check protocols
Click or hover above images to see image description for Anti-Wnt3 antibody.
Check alternative names for the antibodyExpand
|Int 4 antibody|INT4 antibody|MGC131950 antibody|MGC138321 antibody|MGC138323 antibody|Proto-oncogene Int-4 homolog antibody|Proto-oncogene Wnt-3 antibody|wingless type MMTV integration site family member 3 antibody|Wnt 3 proto oncogene protein antibody|WNT 3 proto oncogene protein precursor antibody|wnt3 antibody|WNT3_HUMAN antibody|Anti-Wnt3 antibody (ab32249)
SCBT cat No:
|Catalogue No.|| |
Purified recombinant human Wnt3 protein fragments expressed in E.coli.
|Recommended dilution|| |
WB 1:500-2000; ELISA 1:10000-20000
|Molecular weight|| |
Anti-Wnt3 antibody was tube-contained in liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Anti-Wnt3 antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Int 4 antibody, INT4 antibody, MGC131950 antibody, MGC138321 antibody, MGC138323 antibody, Proto-oncogene Int-4 homolog antibody, Proto-oncogene Wnt-3 antibody, wingless type MMTV integration site family member 3 antibody, Wnt 3 proto oncogene protein antibody, WNT 3 proto oncogene protein precursor antibody, wnt3 antibody, WNT3_HUMAN antibody
|Database links|| |
|Protein function|| |
Ligand for members of the frizzled family of seven transmembrane receptors. Wnt-3 and Wnt-3a play distinct roles in cell-cell signaling during morphogenesis of the developing neural tube (By similarity). .
|Involvement in disease|| |
Tetraamelia syndrome, autosomal recessive (TETAMS) [MIM:273395]: A rare human genetic disorder characterized by complete absence of all four limbs and other anomalies such as craniofacial, nervous system, pulmonary, skeletal and urogenital defects. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the Wnt family.
|Protein post-translational modifications|| |
Palmitoleylation is required for efficient binding to frizzled receptors. Depalmitoleylation leads to Wnt signaling pathway inhibition. .
|Protein cellular localization|| |
Secreted, extracellular space, extracellular matrix.
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St John’s Laboratory Ltd.
|Product type|| |
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