EML1 antibody (clone 5G3), anti-human

EML1 antibody (clone 5G3), anti-human

€435.00
In stock
SKU
AC-AT1900a
Catalog Number: AC-AT1900a
Size: 200 µl
Isotype: mouse IgM Kappa
Applications: WB
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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]

Other Names:
Echinoderm microtubule-associated protein-like 1, EMAP-1, HuEMAP-1, EML1, EMAP1, EMAPL, EMAPL1

Antigen Type:
Recombinant Protein

Gene Name: EML1
Gene ID: 2009
NCBI Accession: NP_001008707.1;NP_004425.2
Primary Accession: O00423
Other Accession: NM_001008707
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
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