GTF2IRD1 Antibody
CATALOG NUMBER: 59-658- Clonality: Polyclonal
- Tested Applications: WB
- Host Species: Rabbit
- Species Reactivity: Human
- Conjugate: Unconjugated
- Size: 400 ul
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- HOST SPECIES: Rabbit
- SPECIES REACTIVITY: Human
- IMMUNOGEN: This GTF2IRD1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 79-108 amino acids from the N-terminal region of human GTF2IRD1.
- CONJUGATE: Unconjugated
- TESTED APPLICATIONS: WB
- APPLICATION NOTE: For WB starting dilution is: 1:1000
- PREDICTED MOLECULAR WEIGHT: 106 kDa
Properties
- PURIFICATION: This antibody is purified through a protein A column, followed by peptide affinity purification.
- CLONALITY: Polyclonal
- ISOTYPE: Rabbit Ig
- PHYSICAL STATE: Liquid
- BUFFER: Supplied in PBS with 0.09% (W/V) sodium azide.
- CONCENTRATION: batch dependent
- STORAGE CONDITIONS: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
Additional Info
- NCBI OFFICIAL SYMBOL: GTF2IRD1
- ADDITIONAL NAMES: 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
- Protein Accession Number: Q9UHL9
- PROTEIN GI NUMBER: 21263630
- NCBI GENE ID NUMBER: 9569
- USER NOTE: Optimal dilutions for each application to be determined by the researcher.
Background
- The protein encoded by this gene contains five GTF2I-likerepeats and each repeat possesses a potential helix-loop-helix(HLH) motif. It may have the ability to interact with otherHLH-proteins and function as a transcription factor or as apositive transcriptional regulator under the control ofRetinoblastoma protein. This gene plays a role in craniofacial andcognitive development and mutations have been associated withWilliams-Beuren syndrome, a multisystem developmental disordercaused by deletion of multiple genes at 7q11.23. Alternativesplicing results in multiple transcript variants. [provided byRefSeq].
- 1: Antonell, A., et al. J. Med. Genet. 47(5):312-320(2010)
- 2: Palmer, S.J., et al. J. Biol. Chem. 285(7):4715-4724(2010)
- 3: Trynka, G., et al. Gut 58(8):1078-1083(2009)
- 4: Dai, L., et al. Am. J. Med. Genet.149A (3), 302-314 (2009) :
Disclaimer
- FOR RESEARCH USE ONLY
For additional information, visit ProSci's Terms & Conditions Page. - Disclaimer: Optimal dilutions/concentrations should be determined by the end user. The information provided is a guideline for product use. This product is for research use only.
Shipping Info
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$35 Dry Ice Shipment fee may be required on some items.
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