WBS16 Antibody (N-term) Blocking peptide
€363.00
In stock
SKU
AC-BP13957a
Background:
This gene encodes an RCC1-like G-exchanging factor. It isdeleted in Williams syndrome, a multisystem developmental disordercaused by the deletion of contiguous genes at 7q11.23. [provided byRefSeq].
Other Names:
Williams-Beuren syndrome chromosomal region 16 protein, RCC1-like G exchanging factor-like protein, WBSCR16
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP13957a was selected from the N-term region of WBS16. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Gene Name: RCC1L (HGNC:14948)
Gene ID: 81554
Primary Accession: Q96I51
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
This gene encodes an RCC1-like G-exchanging factor. It isdeleted in Williams syndrome, a multisystem developmental disordercaused by the deletion of contiguous genes at 7q11.23. [provided byRefSeq].
Other Names:
Williams-Beuren syndrome chromosomal region 16 protein, RCC1-like G exchanging factor-like protein, WBSCR16
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP13957a was selected from the N-term region of WBS16. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Gene Name: RCC1L (HGNC:14948)
Gene ID: 81554
Primary Accession: Q96I51
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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