MECOM anticorps (AA 81-109)

N° du produit ABIN3031740

Cet anticorps anti-MECOM Polyclonal Lapin (ABIN3031740) détecte spécifiquement MECOM dans WB et ELISA. L’anticorps est réactif avec des échantillons de Souris.

Aperçu rapide pour MECOM anticorps (AA 81-109) (ABIN3031740)

Antigène: MECOM (MDS1 and EVI1 Complex Locus (MECOM))

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MECOM est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-MECOM anticorps

Épitope: AA 81-109

Purification: Antigen affinity purified

Immunogène: A portion of amino acids 81-109 from the human protein was used as the immunogen for this MDS1 antibody.

Isotype: Ig Fraction

Information d'application

Indications d'application: Titration of the MDS1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: In 1X PBS pH 7.4 with 0.09 % sodium azide

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Aliquot the MDS1 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.

Détails sur MECOM

Antigène: MECOM (MDS1 and EVI1 Complex Locus (MECOM))

Autre désignation: MDS1

Sujet: MDS1 is located at 3q26 170-400 kb upstream (telomeric) of EVI1 in the chromosomal region in which some of the breakpoints 5' of EVI1 have been mapped. MDS1 has been identified as a single gene as well as a previously unreported exon (s) of EVI1. MDS1 exists in normal tissues both as a unique transcript and as a normal fusion transcript with EVI1, with an additional 188 codons at the 5' end of the previously reported EVI1 open reading frame. In cells with translocation t (3,21), additional fusion transcripts are AML1-MDS1 and AML1-MDS1-EVI1. EVI1 and MDS1 are involved in leukemia associated with chromosomal translocation breakpoints in the region between these genes.

UniProt: Q13465