| 产品详情 |
| Edit |   |
|---|
| Product Name | Human Putative methyltransferase NSUN5 (NSUN5) ELISA Kit |
|---|
| Description | NSUN5 encodes a member of the evolutionarily conserved NOL1/NOP2/Sun domain family. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. WBSCR20 encodes a novel protein expressed in skeletal muscle with similarity to p120 (NOL1), a 120-kDa proliferation-associated nucleolar antigen, a member of an evolutionarily c |
|---|
| Size | 48-strip-wells, 96-strip-wells, 5x96-strip-wells, 10x96-strip-wells, |
|---|
| Concentration | n/a |
|---|
| Applications | n/a |
|---|
| Other Names | [probable 28S rRNA (cytosine-C(5))-methyltransferase isoform 3; Probable 28S rRNA (cytosine-C(5))-methyltransferase; probable 28S rRNA (cytosine-C(5))-methyltransferase; NOP2/Sun RNA methyltransferase family member 5; NOL1-related protein; NOL1R; NOL1/NOP2/Sun domain family member 5; Williams-Beuren syndrome chromosomal region 20A protein] |
|---|
| Gene, Accession, CAS # | NSUN5, Gene ID: 55695, NCBI: NP_001161819.1, UniProt: Q96P11 |
|---|
| Catalog # | MBS282348 |
|---|
| Price | |
|---|
| Order / More Info | Human Putative methyltransferase NSUN5 (NSUN5) ELISA Kit from MYBIOSOURCE INC. |
|---|
| Product Specific References | n/a |
|---|
| 产品资料 |
|
|