NK2 Homeobox 5 anticorps (AA 1-135)

N° du produit ABIN6144644

Détail du produit anti-NK2 Homeobox 5 anticorps

Antigène: NK2 Homeobox 5 (NKX2-5)

Épitope: AA 1-135

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NK2 Homeobox 5 est non-conjugé

Application: Western Blotting (WB)

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

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

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

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

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

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur NK2 Homeobox 5

Antigène: NK2 Homeobox 5 (NKX2-5)

Autre désignation: NKX2-5 (NKX2-5 Produits)

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

Sujet: 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

Poids moléculaire: 11 kDa/16 kDa/34 kDa

ID gène: 1482

UniProt: P52952

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