Transcriptional Enhancer Factor TEF-1 (TEAD1) Antibody
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Description
Tea Domain Family Member 1 (Sv40 Transcriptional Enhancer Factor) Antibody is a Rabbit Polyclonal antibody against Tea Domain Family Member 1 (Sv40 Transcriptional Enhancer Factor).
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Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Target: Transcriptional Enhancer Factor TEF-1 (TEAD1) Immunogen: Human TEAD1. |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Purification | Antigen Affinity Chromatography. |
| Size 1 | 100 µl |
| Form | Liquid |
| Tested Applications | ELISA, WB |
| Buffer | PBS, pH 7.3, containing 0.1% Sodium Azide and 50% Glycerol. |
| Availability | Shipped within 5-10 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | P28347 |
| Gene ID | 7003 |
| NCBI Accession | NP_068780.2, NM_021961.5 |
| OMIM | 108985 |
| Background | Antibody anti-TEAD1 |
| Status | RUO |
| Note | THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION. |
Descripción
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TEAD1 antibody
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.
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Transcriptional Enhancer Factor TEF-1 (TEAD1) Antibody
TEAD1 Antibody is a Rabbit Polyclonal antibody against TEAD1. 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.
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