The Rabbit Polyclonal anti-NKX2-6 antibody has been validated for WB, ELISA, IF and IHC (p). It is suitable to detect NKX2-6 in samples from Human and Mouse.
Catalog No. ABIN6991655
Quick Overview for NKX2-6 antibody (AA 170-220) (ABIN6991655)
NKX2-6 antibody is predicted to not cross-react with other NK2 homeobox family members. At least two isoforms of NKX2-6 are known to exist, this antibody will detect both isoforms
Purification
NKX2-6 Antibody is affinity chromatography purified via peptide column.
Immunogen
NKX2-6 antibody was raised against a 15 amino acid synthetic peptide near the center of human NKX2-6. The immunogen is located within amino acids 170 - 220 of NKX2-6.
NKX2-6
Reactivity: Human
WB, ELISA
Host: Rabbit
Polyclonal
HRP
Application Notes
NKX2-6 antibody can be used for detection of NKX2-6 by Western blot at 1 μ,g/mL. Antibody can also be used for immunohistochemistry starting at 5 μ,g/mL. For immunofluorescence start at 5 μ,g/mL.
Antibody validated: Western Blot in mouse samples, Immunohistochemistry in human samples and Immunofluorescence in human samples. All other applications and species not yet tested.
Restrictions
For Research Use only
Format
Liquid
Concentration
1 mg/mL
Buffer
NKX2-6 Antibody is supplied in PBS containing 0.02 % sodium azide.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C,4 °C
Storage Comment
NKX2-6 antibody can be stored at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
Target
NKX2-6
(NK2 Homeobox 6 (NKX2-6))
Alternative Name
NKX2-6
Background
NKX2-6 Antibody: NKX2-6 (NK2 homeobox 6) is a member of a family of transcription factors that are involved in embryonic development and cell fate. NKX2-6 is a vertebrate homolog of Drosophila homeobox-containing protein called 'tinman', which has been shown to be essential for development of the heart-like dorsal vessel. In conjunction with related gene, NKX2-5, this gene may play a role in both pharyngeal and cardiac embryonic development. Mutations in this gene are thought to be a cause for some congenital heart abnormalities.