T-Box 1 Antikörper

Produktnummer ABIN7254388

Produktdetails anti-T-Box 1 Antikörper

Target: T-Box 1 (TBX1)

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser T-Box 1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Antigen affinity purification

Immunogen: Synthetic peptide of human TBX1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000, IHC 1:25-1:100, ELISA 1:5000-1:10000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.7 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

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 T-Box 1

Target: T-Box 1 (TBX1)

Andere Bezeichnung: TBX1 (TBX1 Produkte)

Synonyme: CAFS antikoerper, CTHM antikoerper, DGCR antikoerper, DGS antikoerper, DORV antikoerper, TBX1C antikoerper, TGA antikoerper, VCFS antikoerper, mp:zf637-3-000616 antikoerper, zgc:136724 antikoerper, TBX1 antikoerper, dgs antikoerper, tga antikoerper, cafs antikoerper, cthm antikoerper, dgcr antikoerper, dorv antikoerper, vcfs antikoerper, tbx1c antikoerper, xtbx1 antikoerper, tbx1 antikoerper, T-box 1 antikoerper, T-box 1 S homeolog antikoerper, T-box 1 L homeolog antikoerper, TBX1 antikoerper, Tbx1 antikoerper, tbx1 antikoerper, tbx1.S antikoerper, tbx1.L antikoerper

Hintergrund: This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene product shares 98 % amino acid sequence identity with the mouse ortholog. DiGeorge syndrome (DGS)/velocardiofacial syndrome (VCFS), a common congenital disorder characterized by neural-crest-related developmental defects, has been associated with deletions of chromosome 22q11.2, where this gene has been mapped. Studies using mouse models of DiGeorge syndrome suggest a major role for this gene in the molecular etiology of DGS/VCFS. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene.

Molekulargewicht:

Observed_MW: Refer to figures

Calculated_MW: 43 kDa

UniProt: O43435

Pathways: Retinoic Acid Receptor Signaling Pathway, Sensory Perception of Sound, Cellular Response to Molecule of Bacterial Origin, Regulation of Muscle Cell Differentiation