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| Reactivity | Human Mouse | 
| Tested applications | WB IHC | 
| Recommended Dilution | WB 1:500 - 1:2000 IHC 1:50 - 1:200 | 
| Calculated MW | 152kDa | 
| Observed MW | Refer to figures | 
| Immunogen | Recombinant protein of human WHSC1 | 
| Storage Buffer | Store at -20℃. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. | 
| Synonym | WHS; NSD2; TRX5; MMSET; REIIBP; | 
This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and has also been involved in the chromosomal translocation t(4;14)(p16.3;q32.3) in multiple myelomas. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Some transcript variants are nonsense-mediated mRNA (NMD) decay candidates, hence not represented as reference sequences.
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