Mesp2 anticorps (AA 1-397)

N° du produit ABIN7869298

Cet anticorps anti-Mesp2 Polyclonal Lapin (ABIN7869298) détecte spécifiquement Mesp2 dans ELISA, WB, IF, FACS et IHC (p). L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour Mesp2 anticorps (AA 1-397) (ABIN7869298)

Antigène: Mesp2 (Mesoderm Posterior 2 Homolog (Mesp2))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Mesp2 est non-conjugé

Application: ELISA, Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-Mesp2 anticorps

Épitope: AA 1-397

Fonction: MESP2 Antibody

Purification: Affinity purified

Immunogène: Recombinant human protein (amino acids M1-Y397) was used as the immunogen for the MESP2 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the MESP2 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the MESP2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur Mesp2

Antigène: Mesp2 (Mesoderm Posterior 2 Homolog (Mesp2))

Autre désignation: MESP2

Sujet: Mesoderm posterior protein 2 (MESP2), also known as class C basic helix-loop-helix protein 6 (bHLHc6), is a protein that in humans is encoded by the MESP2 gene. This gene encodes a member of the bHLH family of transcription factors and plays a key role in defining the rostrocaudal patterning of somites via interactions with multiple Notch signaling pathways. This gene is expressed in the anterior presomitic mesoderm and is downregulated immediately after the formation of segmented somites. This gene also plays a role in the formation of epithelial somitic mesoderm and cardiac mesoderm. Mutations in the MESP2 gene cause autosomal recessive spondylocostal dystosis 2 (SCD02).

UniProt: Q0VG99