DTWD1 Mouse anti-Human, Clone: OTI2D2, lyophilized, TrueMAB™

Mouse Monoclonal Antibody

Supplier:  OriGene CF811568

Catalog No. 50-167-0723

Description

Reconstitute with PBS (pH 7.3) and recommend to perform another round of desalting process using Product No. 7KMWCO

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
• 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: Lyophilized

• Applications: Western Blot
• Clone: OTI2D2
• Formulation: PBS with 8% trehalose and no preservative; pH 7.3
• Gene Accession No.: Q8N5C7
• Gene Symbols: DTWD1
• Immunogen: Full length human recombit protein of human DTWD1 produced in E.coli.
• Quantity: 100 μg
• Primary or Secondary: Primary
• Target Species: Human
• Product Type: Antibody
• Isotype: IgG2b