GTF2IRD1 Overexpression Lysate

Western Blot: GTF2IRD1 Overexpression Lysate (Adult Normal) [NBP2-09820] Left-Empty vector transfected control cell lysate (HEK293 cell lysate); Right -Over-expression Lysate for GTF2IRD1.

• Reactivity: Hu
• Applications: WB

GTF2IRD1 Overexpression Lysate Summary

• Description:

  GTF2IRD1 Transient Overexpression Lysate

  
  Expression Host: HEK293T
  
  Plasmid: RC218834
  
  Accession#: NM_005685
  
  Protein Tag: C-MYC/DDK
  
  You will receive 1 vial of lysate (100ug), 1 vial of empty vector negative control (100ug), and 1 vial of 2xSDS sample buffer (250ul). Each vial of cell lysate contains 100ug of total protein (at 1 mg/ml). The 2xSDS Sample Buffer consists of 4% SDS, 125mM Tris-HCl pH6.8, 10% Glycerol, 0.002% Bromophenol blue, 100mM DTT.
• Gene: GTF2IRD1

Applications/Dilutions

• Dilutions:
  • Western Blot
• Application Notes: This product is intended for use as a positive control in Western Blot. Overexpression of the target protein was confirmed using an antibody to DDK (FLAG) epitope tag (NBP1-71705) present on the protein construct.
  
  Each vial of cell lysate contains 100ug of total protein which should be sufficient for 20-50 reactions. Depending on over-expression level, antibody affinity and detection system, some lysates can go as low as 0.1 ug per load. We recommend starting with 5ug of cell lysate. Add an equal amount of cell lysate and 2X SDS Sample buffer and boil the SDS samples for 10 minutes before loading.
• Theoretical MW: 104.5 kDa.
  Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Packaging, Storage & Formulations

• Storage: Store at -80C. Avoid freeze-thaw cycles.
• Buffer: RIPA buffer

Lysate Details for Array

• Type: Overexpression

Notes

HEK293T cells in 10-cm dishes were transiently transfected with a non-lipid polymer transfection reagent specially designed and manufactured for large volume DNA transfection. Transfected cells were cultured for 48hrs before collection. The cells were lysed in modified RIPA buffer (25mM Tris-HCl pH7.6, 150mM NaCl, 1% NP-40, 1mM EDTA, 1xProteinase inhibitor cocktail mix, 1mM PMSF and 1mM Na3VO4, and then centrifuged to clarify the lysate. Protein concentration was measured by BCA protein assay kit.

Alternate Names for GTF2IRD1 Overexpression Lysate

• 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. Lysates are guaranteed for 6 months from date of receipt.

Bioinformatics

• Gene Symbol: GTF2IRD1