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Nuclear receptor 0B1

ArtNr 18-461-10794
Hersteller GENWAY
Menge 0.05 ml
Kategorie
Typ Antibody
Applikationen IHC
Specific against other
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-5430A3
Similar products 18-461-10794
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Genway ID:
GWB-5430A3
Immunogen:
C-terminal domain of human. Synthetic peptide - KLH conjugated.
Uses: IHC (11 ug/ml) (Optimal dilution to be determined by the researcher)
Function:
Receptor that may be a component of a cascade required for development of steroidogenic tissues. Acts as a dominant negative regulator of transcription mediated by the retinoic acid receptor.
Subunit:
Interacts with COPS2.
Subcellular Location:
Nucleus.
Disease:
Defects in NR0B1 are the cause of X-linked adrenal hypoplasia congenital (AHC) [MIM:300200]. AHC is a developmental disorder of the adrenal gland that results in profound hormonal deficiencies and is lethal if untreated. It is characterized by the absence of the permanent zone of the adrenal cortex and by a structural disorganization of the glands. Hypogonadotropic hypogonadism (HHG) is frequently associated with this disorder. HHG is a condition resulting from or characterized by abnormally decreased gonadal function with retardation of growth and sexual development.
Similarity:
Belongs to the nuclear hormone receptor family. NR0 subfamily. Summary: This protein is a protein that contains a DNA-binding domain. The encoded protein acts as a dominant-negative regulator of transcription which is mediated by the retinoic acid receptor. This protein also functions as an anti-testis gene by acting antagonistically to Sry. Mutations in this gene result in both X-linked congenital adrenal hypoplasia and hypogonadotropic hypogonadism. [1] Mantovani G. De Menis E. Borretta G. Radetti G. Bondioni S. Spada A. Persani L. and Beck-Peccoz P. DAX1 and X-linked adrenal hypoplasia congenita: clinical and molecular analysis in five patients[2] Mantovani G. Mancini M. Gazzano G. Spada A. Colpi G. M. Beck-Peccoz P. and Persani L. Somatic mutational analysis of DAX1 in testes from men with idiopathic azoospermia[3] Saito S. Ito K. Suzuki T. Utsunomiya H. Akahira J. Sugihashi Y. Niikura H. Okamura K. Yaegashi N. and Sasano H. Orphan nuclear receptor DAX-1 in human endometrium and its disorders[4] Achermann J. C. et al. The role of SF1/DAX1 in adrenal and reproductive function[5] Zwermann O. Beuschlein F. Lalli E. Klink A. Sassone-Corsi P. and Reincke M. Clinical and molecular evidence for DAX-1 inhibition of steroidogenic factor-1-dependent ACTH receptor gene expression[6] Zanaria E. Muscatelli F. Bardoni B. Strom T. M. Guioli S. Guo W. Lalli E. Moser C. Walker A. P. McCabe E. R. B. et al. An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita. [7] Guo W. Burris T. P. Zhang Y. H. Huang B. L. Mason J. Copeland K. C. Kupfer S. R. Pagon R. A. McCabe E. R. Genomic sequence of the DAX1 gene: an orphan nuclear receptor responsible for X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism. [8] Strausberg R. L. Feingold E. A. Grouse L. H. Derge J. G. Klausner R. D. Collins F. S. Wagner L. Shenmen C. M. Schuler G. D. Altschul S. F. et al. Generation and initial analysis of more than 15 000 full-length human and mouse cDNA sequences. [9] Altincicek B. Tenbaum S. P. Dressel U. Thormeyer D. Renkawitz R. Baniahmad A. Interaction of the corepressor Alien with DAX-1 is abrogated by mutations of DAX-1 involved in adrenal hypoplasia congenita. [10] Muscatelli F. Strom T. M. Walker A. P. Zanaria E. Recan D. Meindl A. Bardoni B. Guioli S. Zehetner G. Rabl W. et al. Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism.

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Lieferbar: In stock
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