DTWD1 Monoclonal Antibody (OTI1E2), TrueMAB™, OriGene

Mouse Monoclonal Antibody

Supplier:  OriGene TA811573

Catalog No. 50-168-4122

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

• Antigen: DTWD1
• Classification: Monoclonal
• Concentration: 1 mg/mL
• Formulation: PBS with 1% BSA, 50% glycerol and 0.02% sodium azide
• Gene Accession No.: Q8N5C7
• Gene Symbols: DTWD1
• Immunogen: Full length human recombit protein of human DTWD1 produced in E.coli.
• Quantity: 100 μL
• Primary or Secondary: Primary
• Target Species: Human
• Product Type: Antibody
• Isotype: IgG1

• Applications: Western Blot
• Clone: OTI1E2
• Conjugate: Unconjugated
• Gene: DTWD1
• Gene Alias: MDS009
• Host Species: Mouse
• Purification Method: Affinity Chromatography
• Regulatory Status: RUO
• Gene ID (Entrez): 56986
• Content And Storage: -20° C, Avoid Freeze/Thaw Cycles
• Form: Liquid