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Antigenic Specificity | EML1 |
Clone | polyclonal |
Host Species | Rabbit |
Reactive Species | human |
Isotype | n/a |
Format | antigen affinity purified |
Size | 0.1 mL |
Concentration | n/a |
Applications | Western Blot (WB) |
Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
Description | 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. |
Immunogen | Immunogen Type: Peptide Immunogen Description: Synthetic peptide contain a sequence corresponding to a region within amino acids 772 and 834 of EML1 |
Other Names | [echinoderm microtubule-associated protein-like 1 isoform a; Echinoderm microtubule-associated protein-like 1; echinoderm microtubule-associated protein-like 1; echinoderm microtubule associated protein like 1] |
Gene, Accession # | [EML1], Gene ID: 2009, NCBI: NP_001008707 |
Catalog # | MBS9403795 |
Price | $320 |
Order / More Info | EML1 Antibody from MYBIOSOURCE INC. |
Product Specific References | n/a |