Mesp2 antibody (AA 1-397)

Catalog No. ABIN7869298

The Rabbit Polyclonal anti-Mesp2 antibody (ABIN7869298) specifically detects Mesp2 in ELISA, WB, IF, FACS and IHC (p). The antibody is reactive with Human samples.

Quick Overview for Mesp2 antibody (AA 1-397) (ABIN7869298)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Mesp2 antibody is un-conjugated

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

Product Details anti-Mesp2 Antibody

Binding Specificity: AA 1-397

Purpose: MESP2 Antibody

Purification: Affinity purified

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

Isotype: IgG

Application Details

Application Notes: Optimal dilution of the MESP2 antibody should be determined by the researcher.

Restrictions: For Research Use only

Handling

Format: Lyophilized

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

Storage: 4 °C,-20 °C

Storage Comment: 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.

Target Details for Mesp2

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

Alternative Name: MESP2

Background: 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