VSX1 Antikörper (AA 125-154)

Produktnummer ABIN5538275

Produktdetails anti-VSX1 Antikörper

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

Bindungsspezifität: AA 125-154

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser VSX1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This VSX1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 125-154 amino acids from the Central region of human VSX1.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: For WB starting dilution is: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.3 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Store 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.

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. 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.

Molekulargewicht: 38 kDa

Gen-ID: 30813

UniProt: Q9NZR4