Homeobox A11 antibody (AA 74-245)

Catalog No. ABIN3031247

Product Details anti-Homeobox A11 Antibody

Target: Homeobox A11 (HOXA11)

Binding Specificity: AA 74-245

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Homeobox A11 antibody is un-conjugated

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

Purification: Antigen affinity

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

Isotype: IgG

Application Details

Application Notes: 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

Handling

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

Storage: -20 °C

Storage Comment: 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.

Target Details for Homeobox A11

Target: Homeobox A11 (HOXA11)

Alternative Name: HOXA11 (HOXA11 Products)

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

Background: 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.

Gene ID: 3207