NK2 Homeobox 5 Antikörper (AA 1-135)

Produktnummer ABIN6144644

Produktdetails anti-NK2 Homeobox 5 Antikörper

Target: NK2 Homeobox 5 (NKX2-5)

Bindungsspezifität: AA 1-135

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NK2 Homeobox 5 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: MFPSPALTPT PFSVKDILNL EQQQRSLAAA GELSARLEAT LAPSSCMLAA FKPEAYAGPE AAAPGLPELR AELGRAPSPA KCASAFPAAP AFYPRAYSDP DPAKDPRAEK KELCALQKAV ELEKTEADNA ERPRA

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-135 of human NKX2-5 (NP_004378.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu NK2 Homeobox 5

Target: NK2 Homeobox 5 (NKX2-5)

Andere Bezeichnung: NKX2-5 (NKX2-5 Produkte)

Synonyme: CHNG5 antikoerper, CSX antikoerper, CSX1 antikoerper, HLHS2 antikoerper, NKX2.5 antikoerper, NKX2E antikoerper, NKX4-1 antikoerper, VSD3 antikoerper, Csx antikoerper, Nkx-2.5 antikoerper, Nkx2.5 antikoerper, tinman antikoerper, nk2.5 antikoerper, nkx2-5 antikoerper, zgc:111912 antikoerper, AR2 antikoerper, XNkx2-5 antikoerper, csx antikoerper, nkx-2.5 antikoerper, nkx2-5b antikoerper, nkx2.5 antikoerper, NKX2-5 antikoerper, Nkx2-5 antikoerper, csx1 antikoerper, nkx2e antikoerper, XNkx-2.5 antikoerper, CNKX-2.5 antikoerper, NKX-2.5 antikoerper, NK2 homeobox 5 antikoerper, NK2 homeobox 5 S homeolog antikoerper, NKX2-5 antikoerper, Nkx2-5 antikoerper, nkx2.5 antikoerper, nkx2-5.S antikoerper, nkx2-5 antikoerper

Hintergrund: 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.,NKX2-5,CHNG5,CSX,CSX1,HLHS2,NKX2.5,NKX2E,NKX4-1,VSD3,Epigenetics & Nuclear Signaling,Transcription Factors,Cell Biology & Developmental Biology,Neuroscience,Stem Cells,Mesenchymal Stem Cells,Cardiovascular,Cardiovascular Markers,Cardiomyocytes,Heart,Cardiogenesis,NKX2-5

Molekulargewicht: 11 kDa/16 kDa/34 kDa

Gen-ID: 1482

UniProt: P52952

Pathways: Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development