NSUN5 Polyclonal Antibody BT-AP12038
Specifications
| 20ul / 50ul / 100ul |
Background:
This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms.
Classification:
Primary antibody
Alternative names:
Putative methyltransferase NSUN5 ;EC 2.1.1.-;NOL1-related protein;NOL1R;NOL1/NOP2/Sun domain family member 5;Williams-Beuren syndrome chromosomal region 20A protein
Species reactivity:
Human, Mouse
Host:
Rabbit
Isotype:
IgG
Immunogen:
Synthesized peptide derived from human protein . at AA range: 320-400
Concentration:
1 mg/ml
Molecular weight:
Applications:
WB, ELISA
Storage:
-20°C for 1 year
More info:
Email: info@sobekbio.com
Orders:
Email: orders@sobekbio.com
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