| 产品详情 |
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| Antigenic Specificity | GTF2IRD1 |
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| Clone | polyclonal |
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| Host Species | Rabbit |
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| Reactive Species | human |
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| Isotype | n/a |
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| Format | purified |
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| Size | 100 µL |
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| Concentration | n/a |
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| Applications | Immunocytochemistry: 1:100-1:1000, Immunofluorescence: 1:100-1:1000, Western Blot: 1:500-1:3000 |
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| Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
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| Description | GTF2IRD1 Polyclonal Antibody. Williams-Beuren syndrome (WBS) is a developmental disorder caused by the hemizygous microdeletion on chromosome 7q11.23. WBS is an autosomal dominant genetic condition that is characterized by physical, cognitive and behavioral traits. The physical traits associated with WBS include facial dysmorphology, vascular stenoses, growth deficiencies, dental anomalies and neurologic and musculoskeletal abnormalities. Mild retardation, a weakness in visual-spatial skills, anxiety and a short attention span are typical cognitive and behavioral traits of WBS patients. The WBSCR11 gene is located within the WBS deletion and may contribute to the developmental symptoms found in WBS because of a loss of the encoded transcrip |
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| Immunogen | n/a |
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| Other Names | BEN, CREAM1, GTF2I repeat domain containing 1, GTF2I repeat domain-containing protein 1, GTF2IRD1, GTF2IRD1, GTF3, MUSTRD1, RBAP2, WBS, WBSCR11, WBSCR12, hMusTRD1alpha1 |
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| Gene, Accession # | Entrez: 9569 |
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| Catalog # | PA5-78295 |
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| Price | |
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| Order / More Info | GTF2IRD1 Antibody from INVITROGEN ANTIBODIES |
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| Product Specific References | n/a |
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