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Invitrogen™ EML1 Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA530016

Catalog No. PIPA530016


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Description

Description

Recommended positive controls: A549, HeLa, HepG2, mouse brain. Predicted reactivity: Mouse (93%), Rat (93%). Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

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
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, 68519
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Liquid
Western Blot
0.62 mg/mL
0.1M tris glycine with 20% glycerol and 0.01% thimerosal; pH 7
O00423, Q05BC3
EML1
Recombinant fragment corresponding to a region within amino acids 32 and 349 of Human EML1.
100 μL
Primary
Human, Mouse
Antibody
IgG
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