![WB analysis of full-length Nkx2.5 (aa1-324)-hIgGFc transfected HEK293 cell lysate using GTX83313 Nkx2.5 antibody [2E1]. WB analysis of full-length Nkx2.5 (aa1-324)-hIgGFc transfected HEK293 cell lysate using GTX83313 Nkx2.5 antibody [2E1].](https://www.genetex.com/upload/website/prouct_img/normal/GTX83313/GTX83313_20170912_WB_w_23061322_701.webp)
WB analysis of full-length Nkx2.5 (aa1-324)-hIgGFc transfected HEK293 cell lysate using GTX83313 Nkx2.5 antibody [2E1].
Nkx2.5 antibody [2E1]
GTX83313
Overview
- SupplierGeneTex
- Product NameNkx2.5 antibody [2E1]
- Delivery Days Customer9
- Application Supplier NoteWB: 1/500 - 1/2000. ELISA: 1/10000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
- ApplicationsWestern Blot, ELISA
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone ID20
- ConjugateUnconjugated
- Gene ID1482
- Target nameNKX2-5
- Target descriptionNK2 homeobox 5
- Target synonymscardiac-specific homeobox 1; CHNG5; CSX; CSX1; HLHS2; homeobox protein CSX; homeobox protein NK-2 homolog E; homeobox protein NKX 2-5; homeobox protein Nkx-2.5; NK2 transcription factor related, locus 5; NKX 2-5; NKX2.5; NKX2E; NKX4-1; tinman homolog; tinman paralog; VSD3
- HostMouse
- IsotypeIgG1
- Protein IDP52952
- Protein NameHomeobox protein Nkx-2.5
- Scientific DescriptionThis 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. [provided by RefSeq, Oct 2009]
- ReactivityHuman
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203