GTF2IRD1 Antibody (2C7)

Product: HPOB

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
Clonality
Monoclonal
Host
Mouse
Gene
GTF2IRD1
Purity
Protein A purified
Innovators Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Learn about the Innovators Reward

Applications/Dilutions

Dilutions
  • Western Blot
  • ELISA
  • Immunocytochemistry/Immunofluorescence
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]

PMID: 8884206