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EML1 Polyclonal Antibody, Invitrogen™

Rabbit Polyclonal Antibody

Supplier:  Thermo Scientific PA5111287

Catalog No. PIPA5111287


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Description

Description

Immunogen sequence: SGVRKETAVP ATKSNIKRTS SSERVSPGGR RESNGDSRGN RNRTGSTSSS

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 categorized 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.
TRUSTED_SUSTAINABILITY
Specifications

Specifications

EML1
Polyclonal
PBS with 40% glycerol and 0.02% sodium azide; pH 7.2
O00423
EML1
Recombinant Protein corresonding to Human EML1
100 μL
Primary
Human
Antibody
IgG
Immunohistochemistry
Unconjugated
EML1
1110008N23Rik; A930030P13Rik; AA171013; AI847476; AI853955; echinoderm microtubule associated protein like 1; echinoderm microtubule associated protein-like protein 1; echinoderm microtubule-associated protein-like 1; ELP79; EMAP; EMAP1; EMAP-1; EMAPL; EMAPL1; Eml1; HuEMAP; huEMAP-1
Rabbit
Antigen affinity chromatography
RUO
2009
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Liquid
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