MESP2 Monoclonal Antibody (1B3F9), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIMA517121-Each-of-1 | In Stock | ₹ 50,062.50 |
PIMA517121 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 50,062.50
GST (18%): ₹ 9,011.25
Total Price: ₹ 59,073.75
Antigen
MESP2
Classification
Monoclonal
Concentration
1 mg/mL
Formulation
PBS with 0.05% sodium azide
Gene Accession No.
Q0VG99
Gene Symbols
Mesp2
Immunogen
Purified recombinant fragment of human MESP2 (amino acids: 37-94 ) expressed in E. Coli.
Quantity
100 μg
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG1
Applications
ELISA, Western Blot
Clone
1B3F9
Conjugate
Unconjugated
Gene
Mesp2
Gene Alias
bHLHc6; Class C basic helix-loop-helix protein 6; mesoderm posterior 2; mesoderm posterior 2 homolog; mesoderm posterior basic helix-loop-helix transcription factor 2; mesoderm posterior bHLH transcription factor 2; mesoderm posterior protein 2; Mesp2; SCDO2
Host Species
Mouse
Purification Method
Protein G
Regulatory Status
RUO
Gene ID (Entrez)
145873
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Related Products
Description
- 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
- 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).