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Williams-Beuren Syndrome Chromosomal Region 27 Protein (WBSCR27) Antibody
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Catalogue No: abx025778
Price:
US$326.25
(Size: 80 µl)
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WBSCR27 encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23.
Research Articles on Williams-Beuren Syndrome Chromosomal Region 27 Protein (WBSCR27)
| Target | Williams-Beuren Syndrome Chromosomal Region 27 Protein (WBSCR27) |
| Clonality | Polyclonal |
| Reactivity | Human |
| Tested Applications | ELISA, WB, IHC |
| Host | Rabbit |
| Recommended dilutions | WB: 1/1000, IHC-P: 1/50 - 1/100. Not tested in IHC-F. Optimal dilutions/concentrations should be determined by the end user. |
| Conjugation | Unconjugated |
| Immunogen | KLH-conjugated synthetic peptide between 5-34 amino acids from the N-terminal region of human WBSCR27. |
| Isotype | IgG |
| Form | Liquid |
| Purification | Purified through a protein A column, followed by peptide affinity purification. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| UniProt Primary AC | Q8N6F8 (UniProt, ExPASy) |
| UniProt Entry Name | MET27_HUMAN |
| Gene Symbol | METTL27 |
| KEGG | hsa:155368 |
| String | 9606.ENSP00000297873 |
| Molecular Weight | Calculated MW: 26.5 kDa |
| Buffer | PBS containing 0.09% sodium azide. |
| Availability | Shipped within 5-10 working days. |
| Note | This product is for research use only. |
