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EML1 Antibody (monoclonal) (M01)Purified Mouse Monoclonal Antibody (Mab)
| Country | United States
Ordering Information
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| Catalog # | Size | Availability | Price | |
| AT1900a | 200 uL 400 ul | 7-10 days | $ 315.00 | DISCONTINED INQUIRE CLICK INQUIRE Add to cart |
- Specification
- Citiations : 0
- Reviews
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- Backgrounds
EML1 Antibody (monoclonal) (M01) - Product info | |
| Application | WB
|
| Primary Accession | - |
| Reactivity | Human |
| Isotype | IgM Kappa |
| Clone Names | 5G3 |
EML1 Antibody (monoclonal) (M01) - Additional info | |
| Other Names ELP79, EMAP, EMAPL, FLJ45033, HuEMAP echinoderm microtubule associated protein like 1 | |
| Target/Specificity EML1 (-, 1 a.a. ~ 100 a.a) partial recombinant protein with GST tag. | |
| Dilution WB~~1:500~1000 | |
| Format Clear, colorless solution in phosphate buffered saline, pH 7.2 . | |
| Storage Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. | |
| Precautions EML1 Antibody (monoclonal) (M01) is for research use only and not for use in diagnostic or therapeutic procedures. | |
EML1 Antibody (monoclonal) (M01) - Application data
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EML1 monoclonal antibody (M01A), clone 5G3 Western Blot analysis of EML1 expression in HepG2 ( Cat # L019V1 ).
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BACKGROUND
Human echinoderm microtubule-associated protein-like is a strong candidate for the Usher syndrome type 1A gene. Usher syndromes (USHs) are a group of genetic disorders consisting of congenital deafness, retinitis pigmentosa, and vestibular dysfunction of variable onset and severity depending on the genetic type. The disease process in USHs involves the entire brain and is not limited to the posterior fossa or auditory and visual systems. The USHs are catagorized as type I (USH1A, USH1B, USH1C, USH1D, USH1E and USH1F), type II (USH2A and USH2B) and type III (USH3). The type I is the most severe form. Gene loci responsible for these three types are all mapped. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq]
