NKX2.5 Antibody| F45607-0.08ML/F45607-0.4ML/F53210-0.05ML/F53210-0.2ML/R35130-100UG

NKX2.5 Antibody| F45607-0.08ML/F45607-0.4ML/F53210-0.05ML/F53210-0.2ML/R35130-100UG | Gentaur UK, US & Europe Distribution

Background: 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.

Format: Antigen affinity purified

Clone: N/A

Host Animal: Rabbit

Clonality: Polyclonal (rabbit origin)

Isotype: Rabbit Ig

Species Reactivity: Human, Mouse

Predicted Spacies Reactivity: N/A

Application: WB, ELISA

Application Details: Western blot: 1:1000

Application Note: Titration of the NKX2.5 antibody may be required due to differences in protocols and secondary/substrate sensitivity.

Status: Available

Buffer: N/A

Limitation: This NKX2.5 antibody is available for research use only.

Purity: Antigen affinity

Immunogen: A portion of amino acids 2-5 from the human protein was used as the immunogen for this NKX2.5 antibody.

Storage: Aliquot the NKX2.5 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Localization: N/A