EML1 antibody

Catalog No. ABIN7468291

The Rabbit Polyclonal anti-EML1 antibody is suitable to detect EML1 in samples from Human. It has been validated for WB.

Quick Overview for EML1 antibody (ABIN7468291)

Target: EML1 (Echinoderm Microtubule Associated Protein Like 1 (EML1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This EML1 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-EML1 Antibody

Cross-Reactivity: Human, Mouse

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human EML1. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: Mouse brain , A549

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.62 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

Preservative: Thimerosal (Merthiolate)

Precaution of Use: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for EML1

Target: EML1 (Echinoderm Microtubule Associated Protein Like 1 (EML1))

Alternative Name: EMAP like 1

Background:

Synonyms: EMAP like 1 , BH , ELP79 , EMAP , EMAPL , HuEMAP

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]

Molecular Weight: 90 kDa

Gene ID: 2009

UniProt: O00423