Purified Recombinant Rabbit Monoclonal Antibody
| 货号 | 规格 | 价格 |
|---|---|---|
| R011985 | ||
| 20µL | ¥588.00 | |
| 50µL | ¥1080.00 | |
| 100µL | ¥1780.00 |
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| Product Name | Anti-TEF1/TEAD-1 Rabbit mAb |
|---|---|
| Description | Purified Recombinant Rabbit Monoclonal Antibody |
Application
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WB, IHC-P/IF (Tissue-P), IF (Cell)/ICC, ELISA |
| Dilution | WB 1:1,000~1:5,000; IHC-P 1:100~1:200; IF 1:100~1:200 |
| Reactivity | Rat, Human |
| Host | Rabbit |
| Clonality | Monoclonal |
| Clone No. | 81L51L45 |
| Isotype | IgG |
| Label | Unconjugated |
| Immunogen | A synthesized peptide derived from human TEAD-1 |
| Format | Affinity purified monoclonal antibody supplied in PBS with 0.01% sodium azide and 50% glycerol, pH 7.3. |
| Synonyms | AA, Atrophia areata peripapillary chorioretinal degeneration, NTEF 1, NTEF-1, NTEF1, Protein GT IIC, Protein GT-IIC, REF 1, REF1, SV40 transcriptional enhancer factor, TCF 13, TCF-13, TCF13, TEA domain family member, TEA domain family member 1 (SV40 transcriptional enhancer factor), TEA domain family member 1, TEAD 1, TEAD 1 protein, TEAD-1, TEAD1, TEAD1 protein, TEAD1_HUMAN, TEF 1, TEF1, Transcription factor 13 (SV40 transcriptional enhancer factor), Transcription factor 13, Transcriptional enhancer factor 1, Transcriptional enhancer factor TEF-1, Transcriptional enhancer factor TEF1, Transcriptional Enhancer Factor TEF 1. |
|---|---|
| Molecular weight | Calculated MW: 48 kDa; Observed MW: 48 kDa |
| Uniprot ID | P28347 |
| Gene ID | 7003 |
| Storage | Shipped on wet ice. Store at -20℃. Stable for 24 months from date of receipt. Aliquoting is unnecessary for -20℃ storage. |
| Precautions | Anti-Transcriptional Enhancer Factor TEF 1 antibody [81L51L45] is for research use only and not for use in diagnostic or therapeutic procedures. |
| Background | This gene encodes a ubiquitous transcriptional enhancer factor that is a member of the TEA/ATTS domain family. This protein directs the transactivation of a wide variety of genes and, in placental cells, also acts as a transcriptional repressor. Mutations in this gene cause Sveinsson's chorioretinal atrophy. Additional transcript variants have been described but their full-length natures have not been experimentally verified. [provided by RefSeq, May 2010] |
|---|
| Cellular Location | Nucleus. |
|---|
| Tissue Location | Preferentially expressed in skeletal muscle. Lower levels in pancreas, placenta, and heart. |
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