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|Tested species reactivity||Rat , Human , Mouse|
|Host / Isotype||Rabbit / IgG|
|Immunogen||Synthetic peptide corresponding to amino acids 63-112 of human WBSCR11|
|Purification||Antigen affinity chromatography|
|Storage buffer||PBS, pH 7.2|
|Contains||0.05% sodium azide|
|Storage Conditions||Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.|
|Tested Applications||Dilution *|
|Western Blot (WB)||1:500-1:1000|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
This antibody detects endogenous protein at a molecular weight of 106 kDa.
Purity is >95% by SDS-PAGE.
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 transcription factor. WBSCR11 is also designated GRF2IRD1, GTF3, Cream1 and MusTRD1 in human and BEN in mouse, due to slight differences in gene structure. WBSCR11 is expressed in all adult tissues as several variants and has discrete spatial and temporal expression during embryogenesis.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
USE B1-binding protein, Williams-Beuren syndrome chromosome region 11, binding factor for early enhancer, general transcription factor 3, general transcription factor III, muscle TFII-I repeat domain-containing protein 1 alpha 1, slow-muscle-fiber enhancer-binding protein, williams-Beuren syndrome chromosomal region 12 protein, Alb-c-myc line 166.8, Alb/c-myc line 166.8, GTF2I repeat domain-containing 1, GTF2I repeat domain-containing protein 1, c-myc line 166.8, general transcription factor II-I repeat domain-containing protein 1, muscle TFII-I repeat domain-containing protein 1, transcription factor GTF3 alpha 2, transcription factor GTF3 gamma 2, GTF2IRD1, CREAM1, GTF3, MUSTRD1, RBAP2, WBSCR11, WBSCR12
ESTM9, hMusTRD1alpha1, Cream1, Gtf2il, Tg(Alb1-Myc)166.8Sst, WBS, X83320, BEN, RBAP2, 1700012P16Rik, MUSTRD1, MusTRD1, CREAM1, WBSCR12, WBSCR11, GTF3