VSX1 Antikörper

Produktnummer ABIN2458182

Produktdetails anti-VSX1 Antikörper

Target: VSX1 (Visual System Homeobox 1 (VSX1))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser VSX1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Aufreinigung: Antibody is purified by peptide affinity chromatography method.

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human VSX1.

Anwendungsinformationen

Applikationshinweise: VSX1 antibody can be used for detection of VSX1 by ELISA at 1:62500. VSX1 antibody can be used for detection of VSX1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

Rekonstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Konzentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Handhabung: As with any antibody avoid repeat freeze-thaw cycles.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: For short periods of storage (days) store at 4 °C. For longer periods of storage, store VSX1 antibody at -20 °C.

Details zu VSX1

Target: VSX1 (Visual System Homeobox 1 (VSX1))

Andere Bezeichnung: VSX1 (VSX1 Produkte)

Synonyme: VSX1 antikoerper, CAASDS antikoerper, KTCN antikoerper, KTCN1 antikoerper, PPCD antikoerper, PPD antikoerper, RINX antikoerper, CHX10-1 antikoerper, CHX10-like antikoerper, visual system homeobox 1 antikoerper, visual system homeobox 1 L homeolog antikoerper, visual system homeobox 1 homolog, chx10-like antikoerper, Vsx1 antikoerper, VSX1 antikoerper, Tsp_01485 antikoerper, vsx1.L antikoerper, vsx1 antikoerper

Hintergrund: VSX1 contains a paired-like homeodomain and binds to the core of the locus control region of the red/green visual pigment gene cluster. VSX1 may regulate expression of the cone opsin genes early in development. Mutations in VSX1 can cause posterior polymorphous corneal dystrophy and keratoconus. Alternatively spliced transcript variants encoding different isoforms have been described.The protein encoded by this gene contains a paired-like homeodomain and binds to the core of the locus control region of the red/green visual pigment gene cluster. The encoded protein may regulate expression of the cone opsin genes early in development. Mutations in this gene can cause posterior polymorphous corneal dystrophy and keratoconus. Alternatively spliced transcript variants encoding different isoforms have been described.

Molekulargewicht: 38 kDa

Gen-ID: 30813

NCBI Accession: NP_055403

UniProt: Q9NZR4