SHOX Antikörper

Produktnummer ABIN2458012

Produktdetails anti-SHOX Antikörper

Target: SHOX (Short Stature Homeobox (SHOX))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SHOX 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 SHOX.

Anwendungsinformationen

Applikationshinweise: SHOX antibody can be used for detection of SHOX by ELISA at 1:312500. SHOX antibody can be used for detection of SHOX 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 SHOX antibody at -20 °C.

Details zu SHOX

Target: SHOX (Short Stature Homeobox (SHOX))

Andere Bezeichnung: SHOX (SHOX Produkte)

Synonyme: si:ch211-134k13.1 antikoerper, zgc:123182 antikoerper, GCFX antikoerper, PHOG antikoerper, SHOXY antikoerper, SS antikoerper, short stature homeobox antikoerper, shox antikoerper, SHOX antikoerper

Hintergrund: This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies.This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.

Molekulargewicht: 32 kDa

Gen-ID: 6473

NCBI Accession: NP_000442

UniProt: O15266