Nkx2.5 Monoclonal Antibody (2E1), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIMA515551-Each-of-1 | In Stock | ₹ 50,062.50 |
PIMA515551 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 50,062.50
GST (18%): ₹ 9,011.25
Total Price: ₹ 59,073.75
Antigen
Nkx2.5
Classification
Monoclonal
Concentration
1.0 mg/mL
Formulation
PBS with 0.03% sodium azide
Gene Accession No.
P52952
Gene Symbols
Nkx2-5
Immunogen
Purified recombinant fragment of human NKX2.5 expressed in E. Coli.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG1
Applications
ELISA, Western Blot
Clone
2E1
Conjugate
Unconjugated
Gene
Nkx2-5
Gene Alias
Cardiac-specific homeobox; cardiac-specific homeobox 1; CHNG5; CSX; CSX1; Drosophila NK2 transcription factor related, locus 5; FLJ52202; FLJ97166; FLJ97195; FLJ97197; FLJ99536; HLHS2; Homeobox protein CSX; homeobox protein NK-2 homolog E; homeobox protein NKX 2-5; homeobox protein Nkx-2.5; NK2 homeobox 5; NK2 transcription factor related locus 5; NK2 transcription factor related, locus 5; NKX 2-5; NKX2.5; Nkx-2.5; Nkx-25; NKX2-5; NKX2E; NKX4-1; rNKx-2.5; tinman; tinman paralog; VSD3
Host Species
Mouse
Purification Method
Protein G
Regulatory Status
RUO
Gene ID (Entrez)
1482
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
- MA5-15551 targets NKX2.5 in indirect ELISA and WB applications, this antibody also shows reactivity with Human samples
- The MA5-15551 immunogen is purified recombinant fragment of human NKX2.5 expressed in E
- Coli
- MA5-15551 detects NKX2.5 which has a predicted molecular weight of approximately 35kDa This gene encodes a homeobox-containing transcription factor
- This transcription factor functions in heart formation and development
- Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases
- Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition
- Alternative splicing results in multiple transcript variants.