Thermo Fisher Scientific MESP2 Monoclonal Antibody (1B3F9)

Applications

Tested Dilution

Publications

Western Blot (WB)

1:500-1:2,000

-

ELISA (ELISA)

1:10,000

-

Product Specifications

Species Reactivity

Human

Host/Isotype

Mouse / IgG1

Class

Monoclonal

Type

Antibody

Clone

1B3F9

Immunogen

Purified recombinant fragment of human MESP2 (amino acids: 37-94 ) expressed in E. Coli. if (typeof window.$mangular === undefined || !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{targetFamily:MESP2,uniProtId:Q0VG99-1,ncbiNodeId:9606,antigenRange:37-94,antigenLength:397,antigenImageFileName:MA5-17121_MESP2_Q0VG99-1_House_mouse.svg,antigenImageFileNamePDP:MA5-17121_MESP2_Q0VG99-1_House_mouse_PDP.jpeg,sortOrder:1}\]; $mangular.isB2BCMGT = false; $mangular.isEpitopesModalImageMultiSizeEnabled = true;

View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

1 mg/mL

Purification

Protein G

Storage buffer

PBS

Contains

0.05% sodium azide

Storage conditions

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Shipping conditions

Ambient (domestic); Wet ice (international)

RRID

AB_2538592

Product Specific Information

MA5-17121 targets MESP2 in indirect ELISA and WB applications and shows reactivity with Human samples.

The MA5-17121 immunogen is purified recombinant fragment of human MESP2 (amino acids: 37-94 ) expressed in E. Coli.

MA5-17121 detects MESP2 which has a predicted molecular weight of approximately 41.8kDa.

Target Information

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).

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.