Rabbit Polyclonal Antibody to NSD2
货号:
P12882
别名:
WHS; TRX5; KMT3F; KMT3G; MMSET; WHSC1; REIIBP
应用:
IHC
反应种属:
Human
抗体类型:
Primary antibody
Swissprot:
O96028
规格:
目录价
在线咨询
Description |
---|
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. [provided by RefSeq, Jul 2008] |
Specification |
|
---|---|
Aliases | WHS; TRX5; KMT3F; KMT3G; MMSET; WHSC1; REIIBP |
Swissprot | O96028 |
Host/Isotype | Rabbit IgG |
Antibody Type | Primary antibody |
Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
Species Reactivity | Human |
Immunogen | Synthetic peptide of human NSD2 |
Formulation | Purified antibody in PBS with 0.05% sodium azide and 50% glycerol. |
Application |
|
---|---|
IHC | 1/25-1/100 |
ELISA | 1/5000-1/10000 |