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GTF2IRD2B Antibody(C-term)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application 
| WB, E |
|---|---|
| Primary Accession | Q6EKJ0 |
| Other Accession | Q86UP8, NP_001003795.1 |
| Reactivity | Human |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | Rabbit IgG |
| Calculated MW | 107233 Da |
| Antigen Region | 467-494 aa |
| Gene ID | 389524 |
|---|---|
| Other Names | General transcription factor II-I repeat domain-containing protein 2B, GTF2I repeat domain-containing protein 2B, Transcription factor GTF2IRD2-beta, GTF2IRD2B |
| Target/Specificity | This GTF2IRD2B antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 467-494 amino acids from the C-terminal region of human GTF2IRD2B. |
| Dilution | WB~~1:1000 |
| Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
| Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
| Precautions | GTF2IRD2B Antibody(C-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
| Name | GTF2IRD2B |
|---|---|
| Cellular Location | Nucleus. |
| Tissue Location | Ubiquitous. |
Thousands of laboratories across the world have published research that depended on the performance of antibodies from Abcepta to advance their research. Check out links to articles that cite our products in major peer-reviewed journals, organized by research category.
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Provided below are standard protocols that you may find useful for product applications.
Background
This gene encodes a glycosylated phosphoprotein with a leucine zipper motif, two helix-loop-helix motifs (I repeats) that are similar to domains found in the TFII-I family of transcription factors, one CHARLIE8 transposable element-like sequence, and a BED zinc finger. This gene lies within a region that is deleted in Williams-Beuren syndrome. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized.
References
Hinsley, T.A., et al. Protein Sci. 13(10):2588-2599(2004)
Tipney, H.J., et al. Eur. J. Hum. Genet. 12(7):551-560(2004)
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