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DTWD1 Monoclonal Antibody (OTI2C2), TrueMAB™, OriGene
Mouse Monoclonal Antibody
Brand: Origene Technologies TA811567
This item is not returnable.
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Description
Encoding 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.Specifications
| DTWD1 | |
| Monoclonal | |
| Unconjugated | |
| DTWD1 | |
| MDS009 | |
| Mouse | |
| Affinity Chromatography | |
| RUO | |
| 56986 | |
| -20° C, Avoid Freeze/Thaw Cycles | |
| Liquid |
| Western Blot | |
| OTI2C2 | |
| PBS with 1% BSA, 50% glycerol and 0.02% sodium azide | |
| Q8N5C7 | |
| DTWD1 | |
| Full length human recombit protein of human DTWD1 produced in E.coli. | |
| 100 μL | |
| Primary | |
| Human | |
| Antibody | |
| IgG2a |
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