anti-Homeobox A11 (HOXA11) Antibodies

In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Additionally we are shipping Homeobox A11 Proteins (5) and and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
HOXA11 3207 P31270
HOXA11 15396 P31311
HOXA11 368057  
How to order from antibodies-online
  • +1 877 302 8632
  • +1 888 205 9894 (toll-free)
  • Order online

Top anti-Homeobox A11 Antibodies at

Showing 10 out of 74 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Delivery Price Details
Cow Rabbit Un-conjugated WB WB Suggested Anti-HOXA11 Antibody Titration: 0.2-1 ug/mlELISA Titer: 1:312500Positive Control: Transfected 293T 100 μL 2 to 3 Days
Cow Rabbit Un-conjugated IHC, WB Immunohistochemistry with Uterus tissue at an antibody concentration of 5µg/ml using anti-HOXA11 antibody (ARP37064_P050) WB Suggested Anti-HOXA11 Antibody Titration:  0.2-1 ug/ml  ELISA Titer:  1:312500  Positive Control:  Human Uterus 100 μL 2 to 3 Days
Cow Rabbit Un-conjugated WB Host: Rabbit Target Name: HOXA11 Sample Type: Ovary Tumor lysates Antibody Dilution: 1.0ug/ml 100 μL 2 to 3 Days
Human Rabbit Un-conjugated WB Anti- HOXA11 antibody, Western blotting All lanes: Anti HOXA11  at 0.5ug/ml WB: Recombinant Human HOXA11 Protein 0.5ng Predicted bind size: 38KD Observed bind size: 38KD 100 μg 4 to 6 Days
Human Mouse Un-conjugated ELISA, IHC, IHC (p), WB 100 μg 11 to 14 Days
Guinea Pig Rabbit Un-conjugated IHC, IHC (p), WB Anti-HOXA11 antibody IHC staining of human uterus. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval. Antibody  ABIN959058 concentration 5 ug/ml. Anti-HOXA11 antibody IHC of human uterus. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval. Antibody concentration 5 ug/ml. This image was taken for the unconjugated form of this product. Other fo ... 100 μL 11 to 14 Days
Bat Rabbit Un-conjugated WB 100 μL 11 to 14 Days
Human Rabbit Un-conjugated ELISA, IHC, WB Western blot analysis of HOXA11 using COS7 whole cell lysates ABIN6279487 at 1/100 staining Mouse spleen tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary 100 μL 11 to 12 Days
Human Rabbit Un-conjugated IHC, WB Western blot analysis of extracts of various cell lines, using HOXA11 antibody (ABIN1873073) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 30s. 100 μL 11 to 13 Days
Human Mouse Un-conjugated IF, ELISA, WB Immunofluorescence of monoclonal antibody to HOXA11 on HeLa cell. [antibody concentration 10 ug/ml] HOXA11 monoclonal antibody (M08), clone 5A3. Western Blot analysis of HOXA11 expression in Raw 264.7. 100 μg 11 to 12 Days

More Antibodies against Homeobox A11 Interaction Partners

Human Homeobox A11 (HOXA11) interaction partners

  1. HOXA11 high expression might lead to the occurrence and development of lung squamous cancer.

  2. we uncovered a novel potential regulatory mechanism between HOTTIP and one of its physical HOXA clusters, HOXA11. Hence, HOTTIP may mediate, at least partly, HOXA11 expression involved in cell growth, migration, and apoptosis of breast cancer MCF-7 cells.

  3. We conclude that the expression patterns of HoxA10, HoxA11, and HoxA13 and their actions in regulating CAP genes in the uterus create regionalized myometrium phenotypes in women that may be important to control regionalized myometrium contractility for maintaining pregnancy.

  4. High expression of lncRNA HOXA11-AS promotes breast cancer invasion and metastasis by affecting EMT.

  5. HOXA11 silencing suppressed osteosarcoma cell proliferation, invasion and induced cell arrest.

  6. Results show that aberrant hypermethylation and the methylation-induced down-regulation of HOXA11 may promote lung adenocarcinoma progression.

  7. Hypermethylation of HOXA11 is an independent prognostic biomarker in breast cancer. Suggest HOXA11 as a potential tumor suppressor.

  8. The treatment resistance induced by the underexpression of HOXA11 can contribute to a poor prognosis in GBM.

  9. These results suggest that mutations in the coding sequence of HOXA11 might not be a common cause of cryptorchidism, while common polymorphisms in the HOXA11 gene might contribute to the risk of developing unilateral cryptorchidism.

  10. demonstrated that HOXA11-antisense(AS) functioned as a molecular sponge for miR-124, and overexpression of miR-124 attenuated the proliferation and invasion-promoting effect of HOXA11-AS

  11. Bioinformatics prediction forecast that miR-140-5p directly targeted HOXA11-antisense RNA at 3'-UTR, which was confirmed by luciferase reporter assay

  12. HOXA11-AS functions as a competing endogenous RNA.

  13. our study demonstrated that HOXA11 function as a tumor suppressor in renal cell carcinoma

  14. Regulated HOXA10 and HOXA11 expression is necessary for endometrial receptivity; decreased HOXA10 or HOXA11 expression leads to decreased implantation rates. Alternation of HOXA10 and HOXA11 expression has been identified as a mechanism of the decreased implantation associated with endometriosis, polycystic ovarian syndrome, leiomyoma, polyps, adenomyosis, and hydrosalpinx.

  15. Laparoscopic endometrioma resection increases peri-implantation endometrial HOXA-11 mRNA expression.

  16. Epigenetic silencing of HOXA11 promotes gastric cancer proliferation, migration and invasion through activation of Wnt signaling.

  17. The overexpression of miR-30d or 181a suppressed HOXA11 mRNA.

  18. Low HOXA11 expression is associated with hepatocellular carcinoma.

  19. Mutations in the coding region of HOXA11 are not common in Chinese women with Mullerian duct anomalies.

  20. Study suggests that HOXA11 hypermethylation may contribute to the progression of NSCLC by promoting cell proliferation or migration.

Mouse (Murine) Homeobox A11 (HOXA11) interaction partners

  1. miR-23a cluster knockdown in calvarial osteoblasts of these mice increased the recruitment of HOXA5 and HOXA11, with a substantial enrichment of promoter histone H3 acetylation. Taken together, these findings demonstrate that the miR-23a cluster is required for maintaining stage-specific HoxA factor expression during osteogenesis.

  2. the derived functional cooperativity between HOXA11 and FOXO1 is due to derived allosteric regulation of HOXA11 by FOXO1.

  3. On the basis of the polydactyly that we observed after expression of Hoxa11 in distal limbs, we propose that the evolution of Hoxa11 regulation contributed to the transition from polydactyl limbs in stem-group tetrapods to pentadactyl limbs in extant tetrapods.

  4. Shox2 expression restricted to the proximal limb along with Hoxd9 and Hoxa11 expression, juxtaposing the distal expression of Hoxa13 and Hoxd13.

  5. Hoxa-11 maintains cell proliferation in the mouse gubernaculum to facilitate testicular descent.

  6. Hoxa11 and Hoxd11 regulate chondrocyte differentiation upstream of Runx2 and Shox2 in mice.

  7. Results reveal that Hoxa11 knockdown in the uterosacral ligaments and uterus increases extracellular matrix degradation.

  8. Data show that the extra-embryonic function of Hoxa10, -11, and -13 genes stems from their specific expression in the allantois, an extra-embryonic hallmark of amniote vertebrates.

  9. Hox11 genes (Hoxa11, Hoxc11 and Hoxd11) co-regulate and coordinate the development of zeugopod skeletal elements and adjacent elbow and knee joints, and dictate joint identity, morphogenesis and anatomical and functional organization.

  10. mice individually mutant for Hoxa11 or Hoxd11 show no discernible kidney abnormalities. Hoxa11/Hoxd11 double mutants, however, demonstrate hypoplasia of the kidneys

  11. Hoxa11 is required for proper cellular proliferation and apoptotic responses in the developing neonatal uterus.

  12. malformation of the forelimb zeugopod in Hoxa11/Hoxd11 double mutants is a consequence of interruption at multiple steps during the formation of the radius and ulna

  13. Hoxa-11 and Hoxa-13 are involved in the negative regulation of MyoD expression in limb muscle precursors

  14. identify the multiple molecular pathways downstream of Hoxa11/Hoxd11 function in the developing kidney

  15. Yin Yang 1 represses Hoxa11-dependent transcription via interactions with the Hox proteins and Histone Deacetylase recruitment

  16. HOXA11 is critical for development and maintenance of uterosacral ligaments and deficient in pelvic prolapse.

  17. mice mutant for Hoxd11 and Hoxa11 show absence of radius and ulna, anterior homeotic transformation of vertebra, and severe kidney defects, suggesting Hoxd11 and Hoxa11 act together to specify limb outgrowth and patterning of proximodistal axis

Rabbit Homeobox A11 (HOXA11) interaction partners

  1. The TM-induced characteristic changes in the expression pattern of Hoxa11 and Bmp4 on GDs 10 and/or 11 were not noted

Xenopus laevis Homeobox A11 (HOXA11) interaction partners

  1. re-expression of hoxa11 and hoxa13 in the froglet blastema is initiated although the subsequent proximal-distal patterning, including separation of the hoxa11 and hoxa13 expression domains, is disrupted.

Homeobox A11 (HOXA11) Antigen Profile

Protein Summary

In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. This gene is involved in the regulation of uterine development and is required for female fertility. Mutations in this gene can cause radio-ulnar synostosis with amegakaryocytic thrombocytopenia.

Gene names and symbols associated with anti-Homeobox A11 (HOXA11) Antibodies

  • homeobox A11 (HOXA11) antibody
  • homeobox A11 (Hoxa11) antibody
  • homeobox A11 (HOXA11B) antibody
  • homeobox A11 S homeolog (hoxa11.S) antibody
  • GHOX1I antibody
  • Hox-1.9 antibody
  • HOX1 antibody
  • HOX1I antibody
  • Hoxa-11 antibody
  • Hoxa10 antibody
  • HOXA11 antibody
  • RGD1564605 antibody
  • RGD1566402 antibody
  • Xhoxa11 antibody

Protein level used designations for anti-Homeobox A11 (HOXA11) Antibodies

homeo box 1I , homeobox protein HOXA11 , homeobox protein Hox-1I , homeobox protein Hox-A11 , homeo box A11 , homeobox protein Hox-1.9 , chox-1.9 , ghox-1I , homeodomain-containing protein , homeobox A11 , homeo box A10 , homeobox protein A10 , homeobox containing transcription factor , homeobox protein Hox A11

3207 Homo sapiens
15396 Mus musculus
395327 Gallus gallus
397188 Sus scrofa
463312 Pan troglodytes
699490 Macaca mulatta
100137364 Papio anubis
100328790 Oryctolagus cuniculus
368057 Rattus norvegicus
398250 Xenopus laevis
100683897 Canis lupus familiaris
100336578 Bos taurus
100727027 Cavia porcellus
Selected quality suppliers for anti-Homeobox A11 (HOXA11) Antibodies
Did you look for something else?