GTF2IRD1 Antibody [mFluor Violet 610 SE]

• Reactivity: Hu
• Applications: IHC, IP
• Clonality: Polyclonal
• Host: Rabbit
• Conjugate: mFluor Violet 610 SE

GTF2IRD1 Antibody [mFluor Violet 610 SE] Summary

• Immunogen: The immunogen recognized by this antibody maps to a region between residue 650 and 700 of human general transcription factor 2I repeat domain containing 1 using the numbering given in entry NP_057412.1 (GeneID 9569).
• Isotype: IgG
• Clonality: Polyclonal
• Host: Rabbit
• Gene: GTF2IRD1
• Purity: Immunogen affinity purified

Applications/Dilutions

• Dilutions:
  • Immunohistochemistry
  • Immunohistochemistry-Paraffin
  • Immunoprecipitation
• Application Notes: Optimal dilution of this antibody should be experimentally determined.

Packaging, Storage & Formulations

• Storage: Store at 4C in the dark.
• Buffer: 50mM Sodium Borate
• Preservative: 0.05% Sodium Azide
• Purity: Immunogen affinity purified

Notes

mFluor(TM) is a trademark of AAT Bioquest, Inc. This conjugate is made on demand. Actual recovery may vary from the stated volume of this product. The volume will be greater than or equal to the unit size stated on the datasheet.

Alternate Names for GTF2IRD1 Antibody [mFluor Violet 610 SE]

• 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

GTF2IRD1 is 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.

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

Bioinformatics

• Gene Symbol: GTF2IRD1