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HOXB5 is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. Zusätzlich bieten wir Ihnen HOXB5 Proteine (8) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 73 products:
Human Polyclonal HOXB5 Primary Antibody für FACS, WB - ABIN1882091
Kosaki, Kosaki, Suzuki, Yoshihashi, Takahashi, Sasaki, Tomita, McGinnis, Matsuo: Complete mutation analysis panel of the 39 human HOX genes. in Teratology 2002
Cow (Bovine) Polyclonal HOXB5 Primary Antibody für IHC, WB - ABIN2777303
Fu, Lui, Sham, Cheung, Tam: HOXB5 expression is spatially and temporarily regulated in human embryonic gut during neural crest cell colonization and differentiation of enteric neuroblasts. in Developmental dynamics : an official publication of the American Association of Anatomists 2003
Cow (Bovine) Polyclonal HOXB5 Primary Antibody für WB - ABIN2787516
Wu, Lothe, Ahlquist, Silins, Tropé, Micci, Nesland, Suo, Lind: DNA methylation profiling of ovarian carcinomas and their in vitro models identifies HOXA9, HOXB5, SCGB3A1, and CRABP1 as novel targets. in Molecular cancer 2007
Conserved non-coding elements (CNEs) near the zebrafish hoxb5 genes, were characterized.
HOXB5 acts as a positive modulator by promoting cell proliferative response and invasiveness in ER-positive breast cancer.
HOXB5 may be an important regulator of the Wnt (zeige WNT2 Antikörper)/beta-catenin (zeige CTNNB1 Antikörper) signalling pathway, thereby contributing to gastric cancer progression and metastasis.
Roles of Hoxb5 in the development of vagal and trunk neural crest cells.
Overexpression of HoxB5 enhances blood vessel perfusion in vivo by up-regulation of MCP-1 (zeige CCL2 Antikörper) and IL-6 (zeige IL6 Antikörper) as well as in enhanced leucocyte infiltration and blood vessel remodelling.
HOXB5 and HOXB8 (zeige HOXB8 Antikörper) are frequently expressed in ovarian serous carcinoma, with anatomic site-related differences for cytoplasmic staining. HOXB5 may be affected by chemotherapy in effusions.
The findings for HOXB5 and PHOX2B (zeige PHOX2B Antikörper) provide supportive evidence that genes regulating ENCC proliferation, migration and differentiation could be risk factors for Hirschsprung's disease
A miRNA 7-binding single nucleotide polymorphism (1010A/G) located within 3'-UTR (zeige UTS2R Antikörper) of HOXB5 is associated with gene expression and may be a promising prognostic factor for bladder cancer.
HOXB5, HOXB6 (zeige HOXB6 Antikörper), and HOXB7 (zeige HOXB7 Antikörper) are activated in Barrett esophagus, and the midcluster HOXB gene signature in BE most resembled the colon rather than other GI epithelia.
Single nucleotide polymorphism in HOXB5 gene is associated with childhood obesity.
results support that expression of HOX (zeige MSH2 Antikörper) genes is associated with oral squamous cell carcinoma; over 90% of OSCC samples presented HOXB5 expression versus 60% of non-tumor tissues, it can be suggested that HOXB5 may be related to the malignant phenotypes.
only the Hoxb5(+) hematopoietic stem cells exhibit long-term reconstitution capacity after transplantation in primary transplant recipients and, notably, in secondary recipients
Data indicate that homeobox b5 (Hoxb5) regulated the neural crest (NC)development by directly inducing Forkhead box D3 (zeige FOXD3 Antikörper) gene (Foxd3 (zeige FOXD3 Antikörper)).
The dysregulation of Hoxb5 signaling and early depletion of Neural crest cells contribute to enteric nervous system defect and other neurocristopathies in Hirschsprung disease patients deserves further investigation.
TGF beta (zeige TGFB1 Antikörper) inhibition enhanced airway branching, and Hoxb5 protein cellular localization was more diffuse.
Hoxa5 (zeige HOXA5 Antikörper) and Hoxb5 paralog genes share some functions during lung morphogenesis; Hoxa5 (zeige HOXA5 Antikörper) plays a predominant role.
HoxB5 is necessary and sufficient to activate the cell-intrinsic events that regulate the differentiation of angioblasts and mature endothelial cells from their mesoderm-derived precursors
Ret (zeige RET Antikörper) is a downstream target of Hoxb5 whose perturbation causes Ret (zeige RET Antikörper) haploinsufficiency, impaired NCC (zeige SLC12A3 Antikörper) migration, and hypo/aganglionosis, suggesting that Hoxb5 may contribute to the etiology of Hirschsprung's disease.
This gene is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded protein functions as a sequence-specific transcription factor that is involved in lung and gut development. Increased expression of this gene is associated with a distinct biologic subset of acute myeloid leukemia (AML) and the occurrence of bronchopulmonary sequestration (BPS) and congenital cystic adenomatoid malformation (CCAM) tissue.
, homeobox gene B-5
, homeobox protein Hox-B5a
, homeobox protein Zf-21
, Hox 5
, homeobox B5
, homeo box 2A
, homeo box B5
, homeobox protein HHO.C10
, homeobox protein Hox-2A
, homeobox protein Hox-B5
, homeobox protein Hu-1
, homeobox protein H24.1
, homeobox protein Hox-2.1
, homeobox protein Mu-1