DTWD1 Mouse anti-Human, Clone: OTI2C2, Invitrogen
Mouse Monoclonal Antibody
Manufacturer: Invitrogen MA527492
DescriptionEncoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
|PBS with 1% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3|
|DTW domain-containing protein 1, DTWD1|
|-20° C, Avoid Freeze/Thaw Cycles|
|Full length human recombit protein of DTWD1 produced in E.coli|
We continue to work to improve your shopping experience and your feedback regarding this content is very important to us. Please use the form below to provide feedback related to the content on this product.
Your feedback has been submitted. Fisher Scientific is always working to improve our content for you. We appreciate your feedback.Ok