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DTWD1 Mouse anti-Human, Clone: OTI1D2, Invitrogen™

Mouse Monoclonal Antibody

Manufacturer:  Invitrogen MA527494

Catalog No. PIMA527494


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Description

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

Specifications

DTWD1
Monoclonal
1 mg/mL
PBS with 1% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3
Q8N5C7
DTW domain-containing protein 1, DTWD1
Mouse
IgG2a
100 μL
-20° C, Avoid Freeze/Thaw Cycles
Primary
56986
Immunohistochemistry (Paraffin), Western Blot
OTI1D2
Unconjugated
DTWD1
Liquid
DTWD1
Full length human recombit protein of DTWD1 produced in E.coli
Affinity Chromatography
RUO
Antibody
Monoclonal
Human
Documents
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