GTF2I recombinant monoclonal antibody, clone R01-1F4
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More Files
- More Functions
Western Blot
Western blot analysis of Lane 1: A549 whole cell lysate and Lane 2: HL-60 whole cell lysate with GTF2I recombinant monoclonal antibody, clone R01-1F4 (Cat # RAB04435).
Immunocytochemistry
Immunocytochemistry staining of HeLa cells with GTF2I recombinant monoclonal antibody, clone R01-1F4 (Cat # RAB04435) (green). DAPI was stained the cell nucleus (blue).
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Specification
Product Description
Rabbit recombinant monoclonal antibody raised against human GTF2I.
Antibody Species
Rabbit
Immunogen
Original antibody is raised against a synthetic peptide corresponding to human GTF2I.
Theoretical MW (kDa)
Calculated MW: 112 k
Reactivity
Human
Form
Liquid
Purification
Affinity purification
Isotype
IgG
Recommend Usage
Immunocytochemistry
Immunofluorescence (1:50-1:200)
Immunohistochemistry (1:50-1:100)
Western Blot (1:500-1:1000)
The optimal working dilution should be determined by the end user.Storage Buffer
In 50 mM Tris-Glycine, pH 7.4 (0.15 M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% BSA)
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot
Western blot analysis of Lane 1: A549 whole cell lysate and Lane 2: HL-60 whole cell lysate with GTF2I recombinant monoclonal antibody, clone R01-1F4 (Cat # RAB04435).Immunohistochemistry
Immunocytochemistry
Immunocytochemistry staining of HeLa cells with GTF2I recombinant monoclonal antibody, clone R01-1F4 (Cat # RAB04435) (green). DAPI was stained the cell nucleus (blue).Immunofluorescence
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Gene Info — GTF2I
Entrez GeneID
2969Protein Accession#
P78347Gene Name
GTF2I
Gene Alias
BAP-135, BAP135, BTKAP1, DIWS, FLJ38776, FLJ56355, IB291, SPIN, TFII-I, WBS, WBSCR6
Gene Description
general transcription factor II, i
Gene Ontology
HyperlinkGene Summary
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. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 7, 13 and 21. [provided by RefSeq
Other Designations
BTK-associated protein, 135kD|Bruton tyrosine kinase-associated protein 135|Williams-Beuren syndrome chromosome region 6
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Interactome
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Pathway
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