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WBSCR11 (K94) Polyclonal Antibody-BS2161

WBSCR11 (K94) Polyclonal Antibody-BS2161

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WBSCR11 (K94) Polyclonal Antibody

Catalogue Numbers: BS2161-50, BS2161-100

Sizes: 50µl, 100µl

Product: Rabbit IgG, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2

Swiss-Prot: Q9UHL9

Host: Rabbit

Reactivity: Human

Applications: WB

All Applications: WB: 1:500~1:1000

Background: 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.

Purification and Purity: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).

Storage and Stability: Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.

Specificity: WBSCR11 (K94) polyclonal antibody detects endogenous levels of WBSCR11 protein.

Extra Notes: Western blot (WB) analysis of WBSCR11 (K94) pAb at 1:1000 dilution
Lane1:L02 whole cell lysate(10ug)
Lane2:HepG2 whole cell lysate(10ug)
Lane3:MCF-7 whole cell lysate(10ug)

Bioworld Molecular Weight: ~ 106 kDa

Note: For research use only, not for use in diagnostic procedure.

Alternative Name: General transcription factor II-I repeat domain-containing protein 1; GTF2I repeat domain-containing protein 1; General transcription factor III; MusTRD1/BEN; Muscle TFII-I repeat domain-containing protein 1; Slow-muscle-fiber enhancer-binding protein; USE B1-binding protein; Williams-Beuren syndrome chromosomal region 11 protein; Williams-Beuren syndrome chromosomal region 12 protein; GTF2IRD1; CREAM1; GTF3; MUSTRD1; RBAP2; WBSCR11; WBSCR12

Immunogen: Synthetic peptide, corresponding to amino acids 63-112 of Human WBSCR11.

Conjugate: Unconjugated

Modification: Unmodified

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