Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
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 HOXA10 Kits (8) and HOXA10 Proteins (6) and many more products for this protein.
Showing 10 out of 69 products:
Mouse (Murine) Polyclonal HOXA10 Primary Antibody for WB - ABIN1881425
Gordon, Hassan, Saini, Montecino, van Wijnen, Stein, Stein, Lian: Pbx1 represses osteoblastogenesis by blocking Hoxa10-mediated recruitment of chromatin remodeling factors. in Molecular and cellular biology 2010
Show all 3 references for ABIN1881425
Human Polyclonal HOXA10 Primary Antibody for EIA, IF - ABIN952772
Du, Sarno, Taylor: HOXA10 inhibits Kruppel-like factor 9 expression in the human endometrial epithelium. in Biology of reproduction 2010
Show all 3 references for ABIN952772
Dog (Canine) Polyclonal HOXA10 Primary Antibody for IHC, WB - ABIN2792574
Akbas, Song, Taylor: A HOXA10 estrogen response element (ERE) is differentially regulated by 17 beta-estradiol and diethylstilbestrol (DES). in Journal of molecular biology 2004
Show all 2 references for ABIN2792574
Dog (Canine) Polyclonal HOXA10 Primary Antibody for WB - ABIN2792575
Sugimoto, Nakamura, Okinaka, Hirano, Ono, Shigeno, Shinjo, Ohnishi: HOXA10 expression induced by Abl kinase inhibitors enhanced apoptosis through PI3K pathway in CML cells. in Leukemia research 2008
Reduced expression of HOXA10 is associated with Hydrosalpinx.
To summarize, significant differential methylation of HOXA10 and COMT (show COMT Antibodies) promoter regions was found between the ectopic and eutopic endometrial tissues. This is the first study investigating the methylation of HOXA10 and COMT (show COMT Antibodies) genes and their linkage to endometriosis in Chinese patients.
using both knockdown and knockout approaches we show that Hottip expression is required for activation of the 5' Hoxa genes (Hoxa13 (show HOXA13 Antibodies) and Hoxa10/11) and for retaining Mll1 at the 5' end of Hoxa. Moreover, we demonstrate that artificially inducing Hottip expression is sufficient to activate the 5' Hoxa genes and that Hottip RNA binds to the 5' end of Hoxa
HOXA10 is overexpressed in oral squamous cell carcinoma (OSCC) and its expression is functionally associated with several important biological processes related to oral tumorigenesis, such as proliferation, migration and invasion.
The results demonstrated that mutation in HOXA10 gene contributes to the pathogenesis of cryptorchidism, but may not be a common cause.
The HOXA10 gene in women with endometriosis was hypomethylated compared to controls.
HOXA10 was expressed at a high level in the K562/ADM (show ADM Antibodies) cells, and knockdown of HOXA10 enhances the sensitivity of the K562/ADM (show ADM Antibodies) cells to cytotoxic killing by the therapeutic drug, ADR (show AKR1B1 Antibodies), as a result of the increased intracellular accumulation of ADR (show AKR1B1 Antibodies).
Regulated HOXA10 and HOXA11 (show HOXA11 Antibodies) expression is necessary for endometrial receptivity; decreased HOXA10 or HOXA11 (show HOXA11 Antibodies) expression leads to decreased implantation rates. Alternation of HOXA10 and HOXA11 (show HOXA11 Antibodies) expression has been identified as a mechanism of the decreased implantation associated with endometriosis, polycystic ovarian syndrome, leiomyoma, polyps, adenomyosis, and hydrosalpinx.
The combinatory expression of HOXA10 and CD44 (show CD44 Antibodies) was correlated with poor gastric cancer prognosis.
confirmed that HOXA10 promoted epithelialmesenchymal transition in ovarian cancer cells
study identified an E(2)/P(4) response element of the porcine HOXA10 gene for the first time
investigation of regulation of HOXA10 gene expression by estradiol and/or progesterone in porcine endometrium during estrous.
Homeobox A10 expression in the porcine endometrium is closely related to the implantation process and stimulated by conceptus products.
Hmgn5 (show HMGN5 Antibodies) might act downstream of Hoxa10 to regulate the expression of Cox-2 (show COX2 Antibodies), Vegf (show VEGFA Antibodies) and Mmp2 (show MMP2 Antibodies).
Our results suggest that NA10HD increases the number of gamma-globin-transduced HSCs that engraft, leading to an elevated number of fetal hemoglobin-containing red cells.
we suggest that proper regional decidualization and polyploidy development requires FoxM1 (show FOXM1 Antibodies) signaling downstream of Hoxa10 and cyclin D3 (show CCND3 Antibodies).
these studies demonstrate a previously undescribed role for HoxA10 in terminating emergency granulopoiesis, suggesting an important contribution by Hox (show MSH2 Antibodies) proteins to the innate immune response.
Hoxa10 cooperates with Nkx2-5 (show NKX2-5 Antibodies) to regulate the timing of cardiac mesoderm differentiation.
results show that reduced APC (show APC Antibodies) activity is sufficient to induce formation of epithelial inclusion cysts and support ovarian endometrioid adenocarcinoma development and suggest that induced HOXA10 expression and loss of PTEN (show PTEN Antibodies) are key mechanisms driving endometrioid histotype differentiation and progression
a molecular mechanisms through which increased expression of HoxA10 increases Cdx4 expression by direct CDX4 activation and by Fgf2 (show FGF2 Antibodies)-induced beta-catenin (show CTNNB1 Antibodies) activity. This results in Cdx4-induced HoxA10-expression, creating a positive feedback mechanism
Setbp1 (show SETBP1 Antibodies) promotes the self-renewal of murine myeloid progenitors via activation of Hoxa9 (show HOXA9 Antibodies) and Hoxa10.
found that increased Fgf2 (show FGF2 Antibodies) production by HoxA10-overexpressing myeloid progenitor cells induced a phosphoinositol 3-kinase-dependent increase in beta-catenin (show CTNNB1 Antibodies) protein
Results suggest that maternal obesity impairs fetal skeletal development through down-regulation of the HoxA10 gene, which may lead to an increase in the prevalence of low bone mass in the offspring later in life.
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 that may regulate gene expression, morphogenesis, and differentiation. More specifically, it may function in fertility, embryo viability, and regulation of hematopoietic lineage commitment. Alternatively spliced transcript variants have been described. Read-through transcription also exists between this gene and the downstream homeobox A9 (HOXA9) gene.
, homeobox A10, isoform 1
, homeobox protein Hox-A10-like
, homeo box A10
, homeobox protein 1H
, homeobox protein HOXA10
, homeobox protein Hox-1.8
, homeobox protein Hox-1H
, homeobox protein Hox-A10
, homeobox protein A10