GTF2IRD2B Antibodies

AND GTF2IRD2B ELISA kits, GTF2IRD2B Proteins

Many biological assays use antibodies to detect GTF2IRD2B, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with GTF2IRD2B in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop GTF2IRD2B antibodies...

We validate the specificity of these antibodies to GTF2IRD2B by testing them on tissues known to express GTF2IRD2B positively and negatively. Browse below to find the GTF2IRD2B antibody that suites your experiment. We have 1 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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GTF2IRD2B Infographic by Boster Bio

All GTF2IRD2B Products

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GTF2IRD2B (NM_001003795) Human Over-expression Lysate

Human

$960
Cat # LS389524
20 µg, 100 µg

GTF2IRD2B Overview

Facts about General transcription factor II-I repeat domain-containing protein 2B.

GTF2IRD2B 3D structure. Source: alphafold

General transcription factor II-I repeat domain-containing protein 2B (GTF2IRD2B)

Gene Information

Human
Gene Name:	GTF2IRD2B
Uniprot:	Q6EKJ0
Entrez:	389524

Family

Belongs to:

TFII-I family

Alternative Names

GTF2I Repeat Domain Containing 2B; GTF2I Repeat Domain-Containing Protein 2B; Transcription Factor GTF2IRD2-Beta

Molecular Weight

Mass (kDA):
107.233 kDA

Genomic Context


Human

Location:	7q11.23
Sequence:	7; NC_000007.14 (75092556..75149817)

Tissue Specificity

Ubiquitous.

Subcellular Localizations

Nucleus.

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/GTF2IRD2B

References

PMID: 15100712 by Tipney H.J., et al. Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome.

PMID: 15388857 by Hinsley T.A., et al. Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome.