GTF2IRD2 Antibody / GTF2IRD2 alpha

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NSJ Bioreagents
Product Code: NSJ-V9250
Product Group: Primary Antibodies
Supplier: NSJ Bioreagents
CodeSizePrice
NSJ-V9250-20UG20ug£264.00
Quantity:
NSJ-V9250-100UG100ug£534.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Host Type: Mouse
Antibody Isotype: Mouse IgG2b
Antibody Clonality: Monoclonal
Antibody Clone: PCRP-GTF2IRD2-1B12
Regulatory Status: RUO
Target Species: Human
Applications:
  • Fluorescence-activated cell sorting (FACS)
  • Western Blot (WB)
Storage:
Aliquot the GTF2IRD2 alpha antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Images

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Analysis of HuProt(TM) microarray containing more than 19,000 full-length human proteins using GTF2IRD2 alpha antibody (clone PCRP-GTF2IRD2-1B12). These results demonstrate the foremost specificity of the PCRP-GTF2IRD2-1B12 mAb. Z- and S- score: The Z-score represents the strength of a signal that an antibod
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Analysis of HuProt(TM) microarray containing more than 19,000 full-length human proteins using GTF2IRD2 alpha antibody (clone PCRP-GTF2IRD2-1B12). These results demonstrate the foremost specificity of the PCRP-GTF2IRD2-1B12 mAb. Z- and S- score: The Z-score represents the strength of a signal that an antibod

Documents

Further Information

Application Details :
Flow cytometry: 1-2ug/million cells,Western blot: 1-2ug/ml
Application Note:
Optimal dilution of the GTF2IRD2 alpha antibody should be determined by the researcher.
Description:
The TFII-I family contains two highly homologous 949 amino acid proteins, GTF2IRD2 (also called GTF2IRD2 alpha and GTF2IRD2A) and GTF2IRD2B. Localizing to the nucleus, these proteins are ubiquitously expressed and contain two GTF2I- like repeats. Encoded by a gene mapping to human chromosome 7q11.23, GTF2IRD2 and GTF2IRD2B are located in the Williams-Beuren syndrome (WBS) critical region. The deletion of genes located within this region results in WBS, possibly due to the unequal crossing over of highly homologous low-copy repeat sequences that flank the deleted region. WBS is an autosomal dominant genetic condition that is characterized by physical, cognitive and behavioral traits including facial dysmorphology, vascular stenoses, growth deficiencies, dental anomalies and neurologic and musculoskeletal abnormalities.
Format :
Purified
Formulation :
0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced), 0.05% sodium azide
Immunogen:
Recombinant full-length human General transcription factor II-I repeat domain-containing protein 2A protein was used as the immunogen for the GTF2IRD2 alpha antibody.
Limitation:
This GTF2IRD2 alpha antibody is available for research use only.
Localization:
Nucleus
Microarray Validated?:
Yes
Purity:
Protein A/G affinity
Species Reactivity :
Human
Uniprot #:
Q86UP8