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Mouse Monoclonal Wnt-10b antibody [5A7] (STJ98452)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, IHC, IF, ELISA
Recommended dilution: WB 1:500-1:2000; IHC 1:200-1:1000; IF 1:200-1:1000; ELISA 1:10000
Recommended protocols: check protocols
Click or hover above images to see image description for Wnt-10b Monoclonal Antibody.
Check alternative names for the antibodyExpand
WNT10B antibody, WNT12 antibody,|Protein Wnt-10b antibody|Protein Wnt-12 antibody|SHFM6 antibody|wingless type MMTV integration site family, member 10B antibody|WN10B_HUMAN antibody|WNT 10B protein antibody|WNT 12 antibody|Wnt10b antibody|wnt12 antibody|Anti-Wnt10b antibody (ab70816)
SCBT cat No: To be updated
Wnt-10b Monoclonal Antibody
|Catalogue No.|| |
Wnt-10b Monoclonal Antibody detects endogenous levels of Wnt-10b protein.
Purified recombinant fragment of human Wnt-10b expressed in E Coli
WB, IHC, IF, ELISA
|Recommended dilution|| |
WB 1:500-1:2000; IHC 1:200-1:1000; IF 1:200-1:1000; ELISA 1:10000
Wnt-10b Antibody was tube-contained. Ascitic fluid containing 0.03% sodium azide.
Wnt-10b Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Protein Wnt-10b antibody, Protein Wnt-12 antibody
|Protein names|| |
Protein Wnt-10b , Protein Wnt-12
|Protein function|| |
Ligand for members of the frizzled family of seven transmembrane receptors. Probable developmental protein. May be a signaling molecule which affects the development of discrete regions of tissues. Is likely to signal over only few cell diameters (By similarity).
|Protein tissue specificity|| |
Detected in most adult tissues. Highest levels were found in heart and skeletal muscle. Low levels are found in brain.
|Involvement in disease|| |
Split-hand/foot malformation 6 (SHFM6) [MIM:225300]: A limb malformation involving the central rays of the autopod and presenting with syndactyly, median clefts of the hands and feet, and aplasia and/or hypoplasia of the phalanges, metacarpals, and metatarsals. Some patients have been found to have mental retardation, ectodermal and craniofacial findings, and orofacial clefting. . 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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