TFII-I Antibody

Images

 
Western Blot: TFII-I Antibody [NB100-61053] - Detection of Human GTF2I/TFII-I on HeLa whole cell lysate. GTF2I/TFII-I was also immunoprecipitated by rabbit anti-GTF2I/TFII-I antibody NB100-61054.
Immunohistochemistry: TFII-I Antibody [NB100-61053] - Sample: FFPE section of human breast carcinoma (left) and mouse teratoma (right). Antibody: Affinity purified rabbit anti-GTF2I/TFII-I used at a dilution of 1:200 ...read more

Product Details

Summary
Reactivity Hu, MuSpecies Glossary
Applications WB, IHC-P, IP
Clonality
Polyclonal
Host
Rabbit
Conjugate
Unconjugated
Concentration
0.2 mg/ml
 

Independent Antibodies

       

Order Details

TFII-I Antibody Summary

Immunogen
The immunogen recognized by this antibody maps to a region between residue 935 and 985 of human general transcription factor II, i using the numbering given in entry NP_127492.1 (GeneID 2969).
Isotype
IgG
Clonality
Polyclonal
Host
Rabbit
Gene
GTF2I
Purity
Immunogen affinity purified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • Western Blot 1:2000-1:10000
  • Immunohistochemistry-Paraffin 1:200-1:1000
  • Immunoprecipitation 2-5 ug/mg
Application Notes
Epitope retrieval with citrate buffer pH6.0 is recommended for FFPE tissue sections.

Packaging, Storage & Formulations

Storage
Store at 4C. Do not freeze.
Buffer
TBS and 0.1% BSA
Preservative
0.09% Sodium Azide
Concentration
0.2 mg/ml
Purity
Immunogen affinity purified

Alternate Names for TFII-I Antibody

  • BAP-135,135kD
  • BAP135WBS
  • Bruton tyrosine kinase-associated protein 135
  • BTKAP1
  • DIWS
  • FLJ38776
  • FLJ56355
  • general transcription factor II, i
  • general transcription factor IIi
  • general transcription factor II-I
  • GTFII-I
  • IB291
  • SPINBTK-associated protein 135
  • TFII-ISRF-Phox1-interacting protein
  • WBSCR6
  • Williams-Beuren syndrome chromosome region 6

Background

This gene encodes a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. The exon(s) encoding 5' UTR has not been fully defined, but this gene is known to contain at least 34 exons, and its alternative splicing generates 4 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.

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Video Protocols

WB Video Protocol

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Secondary Antibodies

 

Isotype Controls

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Bioinformatics

Gene Symbol GTF2I
Entrez
Uniprot