MSX1 Monoclonal Antibody (5D11), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIMA515839-Each-of-1 | In Stock | ₹ 50,062.50 |
PIMA515839 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 50,062.50
GST (18%): ₹ 9,011.25
Total Price: ₹ 59,073.75
Antigen
MSX1
Classification
Monoclonal
Concentration
Conc. Not Determined
Formulation
ascites with 0.03% sodium azide
Gene Accession No.
P28360
Gene Symbols
MSX1
Immunogen
Purified recombinant fragment of human MSX1 expressed in E. Coli.
Regulatory Status
RUO
Gene ID (Entrez)
4487
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
ELISA, Western Blot
Clone
5D11
Conjugate
Unconjugated
Gene
MSX1
Gene Alias
AA675338; AI324650; ECTD3; homeo box, msh-like 1; homeobox 7; homeobox protein Hox-7; Homeobox protein MSX-1; homeobox, msh-like 1; Hox7; Hox-7; Hox7.1; hox-7.1; HYD1; msh; msh homeo box 1; msh homeobox 1; msh homeobox 1-like protein; msh homeobox homolog 1; Msx1; muscle-segment homeobox; STHAG1
Host Species
Mouse
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG1
Related Products
Description
- MA5-15839 targets MSX1 in indirect ELISA, WB applications and shows reactivity with Human samples
- The MA5-15839 immunogen is purified recombinant fragment of human MSX1 expressed in E
- Coli
- MA5-15839 detects MSX1 which has a predicted molecular weight of approximately 31kDa
- MSX1 is a member of the muscle segment homeobox gene family
- It functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins
- MSX1 may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition
- Mutations in the gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia.