HOXD12 antibody (Homeobox D12) (AA 211-237) Primary Antibody
- Target See all HOXD12 Antibodies
- AA 211-237
- This HOXD12 antibody is un-conjugated
- ELISA, Western Blotting (WB)
- Antigen affinity purified
- A portion of amino acids 211-237 from the human protein was used as the immunogen for this HOXD12 antibody.
- Ig Fraction
anti-Homeobox D12 (HOXD12) (Middle Region) antibody Primary Antibody
HOXD12 Reactivity: Human, Mouse, Rat, Cow, Dog, Goat, Guinea Pig, Horse, Rabbit, Saccharomyces cerevisiae, Zebrafish (Danio rerio) WB Host: Rabbit Polyclonal unconjugatedanti-Homeobox D12 (HOXD12) (N-Term) antibody Primary Antibody
HOXD12 Reactivity: Human, Mouse, Rat, Bat, Cow, Dog, Guinea Pig, Horse, Monkey, Pig, Rabbit IHC, IHC (p), WB Host: Rabbit Polyclonal unconjugated
- Application Notes
- Titration of the HOXD12 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000
- For Research Use only
- In 1X PBS pH 7.4 with 0.09 % sodium azide
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- -20 °C
- Storage Comment
- Aliquot the HOXD12 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
- Alternative Name
- HOXD12 (HOXD12 Products)
- HOX4H, Hox-4.7, Hox-5.6, HOXD12, HOX-D12, hoxd-12, hoxd12, HoxD12a, homeobox D12, homeo box D12, homeobox D12a, HOXD12, Hoxd12, hoxd12a, hoxd12
- This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. The exact role of this gene has not been determined.