Homeobox A11 Antikörper (AA 74-245)

Produktnummer ABIN3031247

Produktdetails anti-Homeobox A11 Antikörper

Target: Homeobox A11 (HOXA11)

Bindungsspezifität: AA 74-245

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Homeobox A11 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Flow Cytometry (FACS)

Aufreinigung: Antigen affinity

Immunogen: Human partial recombinant protein (AA 74-245) was used as the immunogen for this HOXA11 antibody.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: The stated application concentrations are suggested starting amounts. Titration of the HOXA11 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 0.5-1 μg/mL,FACS: 1-3 μg/10^6 cells

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Lagerung: -20 °C

Informationen zur Lagerung: After reconstitution, the HOXA11 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.

Details zu Homeobox A11

Target: Homeobox A11 (HOXA11)

Andere Bezeichnung: HOXA11 (HOXA11 Produkte)

Synonyme: HOX1 antikoerper, HOX1I antikoerper, Hox-1.9 antikoerper, Hoxa-11 antikoerper, GHOX1I antikoerper, HOXA11 antikoerper, Hoxa10 antikoerper, RGD1564605 antikoerper, RGD1566402 antikoerper, Xhoxa11 antikoerper, homeobox A11 antikoerper, homeobox A11 S homeolog antikoerper, HOXA11 antikoerper, Hoxa11 antikoerper, HOXA11B antikoerper, hoxa11.S antikoerper

Hintergrund: Homeobox protein A11 is a protein that in humans is encoded by the HOXA11 gene. It is mapped to 7p15.2. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is involved in the regulation of uterine development and is required for female fertility. HOXA11 is essential for the development of the uterosacral ligaments, it has been found that women with pelvic organ prolapse may have weakened connective tissue due to changes in this signaling pathway. Mutations in this gene can cause radio-ulnar synostosis with amegakaryocytic thrombocytopenia.

Gen-ID: 3207