GTF2IRD1 Antibody (2C7) Summary
| Immunogen |
GTF2IRD1 (AAH18136, 1 a.a. ~ 960 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.MALLGKRCDVPTNGCGPDRWNSAFTRKDEIITSLVSALDSMCSALSKLNAEVACVAVHDESAFVVSTEKGRMFLNARKELQSDFLRFCRGPPWKDPEAEHPKKVQRGEGGGRSLPRSSLEHGSDVYLLRKMVEEVFDVLYSEALGRASVVPLPYERLLREPGLLAVQGLPEGLAFRRPAEYDPKALMAILEHSHRIRFKLKRPLEDGGRDSKALVELNGVSLIPKGSRDCGLHGQAPKVPPQDLPPTATSSSMAS
|
| Specificity |
Reacts with GTF2I repeat domain containing 1.
|
| Isotype |
IgG2a Kappa
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| Clonality |
Monoclonal
|
| Host |
Mouse
|
| Gene |
GTF2IRD1
|
| Purity |
Protein A purified
|
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|
Applications/Dilutions
| Dilutions |
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| Application Notes |
This antibody is reactive against recombinant protein in western blot and ELISA.
|
Reactivity Notes
Human
Packaging, Storage & Formulations
| Storage |
Store at -20C. Avoid freeze-thaw cycles.
|
| Buffer |
PBS (pH 7.4)
|
| Preservative |
No Preservative
|
| Purity |
Protein A purified
|
Notes
This product is produced by and distributed for Abnova, a company based in Taiwan.
Alternate Names for GTF2IRD1 Antibody (2C7)
- BEN
- CREAM1
- general transcription factor II-I repeat domain-containing protein 1
- General transcription factor III
- GTF2I repeat domain containing 1
- GTF2I repeat domain-containing protein 1
- GTF3GTF2I repeat domain-containing 1
- hMusTRD1alpha1
- muscle TFII-I repeat domain-containing protein 1 alpha 1
- Muscle TFII-I repeat domain-containing protein 1
- MusTRD1
- MusTRD1/BEN
- MUSTRD1general transcription factor 3
- RBAP2WBSCR12binding factor for early enhancer
- Slow-muscle-fiber enhancer-binding protein
- USE B1-binding protein
- WBS
- WBSCR11
- Williams-Beuren syndrome chromosomal region 11 protein
- Williams-Beuren syndrome chromosomal region 12 protein
- Williams-Beuren syndrome chromosome region 11
Background
The protein encoded by this gene contains five GTF2I-like repeats and each repeat possesses a potential helix-loop-helix (HLH) motif. It may have the ability to interact with other HLH-proteins and function as a transcription factor or as a positive transcriptional regulator under the control of Retinoblastoma protein. This gene is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing of this gene generates at least 2 transcript variants. [provided by RefSeq]