EML1 anticorps (AA 772-834)

N° du produit ABIN1886659

Détail du produit anti-EML1 anticorps

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

Épitope: AA 772-834

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp EML1 est non-conjugé

Application: Western Blotting (WB)

Purification: Purified by antigen-affinity chromatography.

Immunogène: Synthetic peptide contain a sequence corresponding to a region within amino acids 772 and 834 of EML1

Information d'application

Indications d'application: Suggested dilutions:
Western blotting: 1.500-1.3000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: 1 x PBS, 1 % BSA, 20 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: Biohazard Informations: This product contains thimerosal which is hazardous.

Stock: 4 °C/-20 °C

Stockage commentaire: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Détails sur EML1

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

Autre désignation: EML1 (EML1 Produits)

Synonymes: anticorps ELP79, anticorps EMAP, anticorps EMAPL, anticorps HuEMAP, anticorps EML1, anticorps MGC108311, anticorps wu:fj01a06, anticorps zgc:153105, anticorps 1110008N23Rik, anticorps A930030P13Rik, anticorps AA171013, anticorps AI847476, anticorps AI853955, anticorps echinoderm microtubule associated protein like 1, anticorps echinoderm microtubule associated protein like 1 S homeolog, anticorps EML1, anticorps eml1.S, anticorps eml1, anticorps Eml1

Sujet: 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]

Poids moléculaire: 92 kDa

ID gène: 2009

NCBI Accession: NM_001008707, NP_001008707