Homeobox A11 anticorps (AA 74-245)

N° du produit ABIN3031247

Détail du produit anti-Homeobox A11 anticorps

Antigène: Homeobox A11 (HOXA11)

Épitope: AA 74-245

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Homeobox A11 est non-conjugé

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

Purification: Antigen affinity

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

Isotype: IgG

Information d'application

Indications d'application: 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

Restrictions: For Research Use only

Stockage

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

Stock: -20 °C

Stockage commentaire: 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.

Détails sur Homeobox A11

Antigène: Homeobox A11 (HOXA11)

Autre désignation: HOXA11 (HOXA11 Produits)

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

Sujet: 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.

ID gène: 3207