推荐产品
生物源
mouse
品質等級
抗體表格
purified immunoglobulin
抗體產品種類
primary antibodies
無性繁殖
HU11B, monoclonal
物種活性
human, rat, rhesus macaque, mouse
技術
affinity binding assay: suitable
electron microscopy: suitable
immunofluorescence: suitable
immunohistochemistry: suitable (paraffin)
同型
IgG1κ
NCBI登錄號
UniProt登錄號
運輸包裝
wet ice
目標翻譯後修改
unmodified
基因資訊
human ... GNRH1(2796)
一般說明
Gonadotropin-releasing hormone I (also known as GnRH, GnRH-I, Gonadoliberin-1, Gonadoliberin I, LHRH, LH-RH I, Luteinizing hormone-releasing hormone I) is encoded by the Gnrh1 (also known as Gnrh, Lhrh1, Lnrh) gene (Gene ID 14714) in murine species. GnRH/LHRH is initially produced as a 90-amino acid progonadoliberin-1 precursor protein (UniProt P13562), removal of the signal peptide (a.a. 1-21) yields progonadoliberin-1 (a.a. 22-90), which is further processed by a proteolytic cleavage to release the GnRH/LHRH decapeptide (a.a. 22-31) and the 56-a.a. prolactin release-inhibiting factor 1 (a.a. 35-90). The LHRH decapeptide functions as the primary endocrine link between the brain and the reproductive system. It plays a primary neuroendocrine role in orchestrating the developmental processes associated with sexual development in immature mammals and also in maintaining normal reproductive function in adults. LHRH-producing neurons are located mainly in the lateral anterior hypothalamus, septum, and medial preoptic area, from where they extend axons towards the median eminence and relese the hormone into the hypothalamo-hypophyseal portal blood vessels in an episodic or pulsatile manner.
特異性
Clone HU11B reacts with C-terminally blocked GnRH-I/LHRH (LHRH-NH2), but not LHRH with a free C-terminal end (LHRH-COOH). Clone HU11B exhibits reduced affinity toward N-terminally truncated LHRH-NH2 and failed to recognize pro-LHRH, Atrial Naturetic Factor/ANF, Growth hormone-releasing hormone/GHRH, Oxytocin, Somatostatin, Thyrotropin-releasing hormone/TRH, and Vasoactive intestinal peptide/VIP (Urbanski, H.F., et al. (1991). Biol. Reprod. 44(4):681-686).
免疫原
Epitope: N-terminus.
Mouse GnRH (QHWSYGLRPG) conjugated to bovine thyroglobulin.
應用
Anti-Gonadotropin-Releasing Hormone Antibody, NT, clone HU11B (Ascites Free) is an antibody against Gonadotropin-Releasing Hormone for use in Immunohistochemistry (Paraffin), Affinity Binding Assay, Immunofluorescence, Electron Microscopy.
Immunohistochemistry Analysis: A 1:50 dilution from a representative lot detected Gonadotropin-Releasing Hormone in human prostate cancer tissue.
Affinity Binding Assay: A representative lot captured C-terminally blocked GnRH-I/LHRH (LHRH-NH2), but not LHRH with a free C-terminal end (LHRH-COOH). Clone HU11B exhibited reduced affinity toward N-terminally truncated LHRH-NH2 and failed to recognize pro-LHRH, Atrial Naturetic Factor/ANF, Growth hormone-releasing hormone/GHRH, Oxytocin, Somatostatin, Thyrotropin-releasing hormone/TRH, and Vasoactive intestinal peptide/VIP (Urbanski, H.F., et al. (1991). Biol. Reprod. 44(4):681-686).
Immunofluorescence Analysis: A representative lot detected GnRH neurons in brain sections from female rhesus monkeys by fluorescent immunohistochemistry (Naugle, M.M., and Gore, A.C. (2014). Neuroendocrinology 100:334-346).
Immunofluorescence Analysis: A representative lot detected pregnancy stage-dependent GnRH-I immunoreactivity in the luminal epithelium of rat oviduct by fluorescent immunohistochemistry using paraformaldehyde-fixed cryosections (Sengupta, A., et al. (2007). J. Histochem. Cytochem. 55(5):525-534).
Immunofluorescence Analysis: A representative lot detected GnRH-I immunoreactivity in frozen mouse hypothalamic sections by fluorescent immunohistochemistry (Olcese, J., et al. (2003). Neuroreport. 14(4):613-618).
Electron Microscopy: A representative lot detected GnRH-I immunoreactivity associated with the luminal epithelium secretory vesicles of rat oviduct by EM using paraformaldehyde-fixed LR wihite sections from rats at day 16 of pregnancy (Sengupta, A., et al. (2007). J. Histochem. Cytochem. 55(5):525-534).
Immunohistochemistry Analysis: A representative lot detected GnRH-I immunoreactivity throughout the hypothalamus in paraformalin-fixed, paraffin-embedded South American plains vizcacha (Lagostomus maximus) brain sections (Dorfman, V.B., et al. (2011). J. Mol. Histol. 42(4):311-321).
Immunohistochemistry Analysis: A representative lot detected GnRH-I-positie neurons in formalin-fixed, paraffin-embedded mouse brain sections (Bergman, J.E., et al. (2010). Eur. J. Hum. Genet. 18(2):171-177).
Immunohistochemistry Analysis: A representative lot detected GnRH-I immunoreactivity in paraformaldehyde-fixed rat brain vibratome sections (Urbanski, H.F., et al. (1991). Biol. Reprod. 44(4):681-686).
Affinity Binding Assay: A representative lot captured C-terminally blocked GnRH-I/LHRH (LHRH-NH2), but not LHRH with a free C-terminal end (LHRH-COOH). Clone HU11B exhibited reduced affinity toward N-terminally truncated LHRH-NH2 and failed to recognize pro-LHRH, Atrial Naturetic Factor/ANF, Growth hormone-releasing hormone/GHRH, Oxytocin, Somatostatin, Thyrotropin-releasing hormone/TRH, and Vasoactive intestinal peptide/VIP (Urbanski, H.F., et al. (1991). Biol. Reprod. 44(4):681-686).
Immunofluorescence Analysis: A representative lot detected GnRH neurons in brain sections from female rhesus monkeys by fluorescent immunohistochemistry (Naugle, M.M., and Gore, A.C. (2014). Neuroendocrinology 100:334-346).
Immunofluorescence Analysis: A representative lot detected pregnancy stage-dependent GnRH-I immunoreactivity in the luminal epithelium of rat oviduct by fluorescent immunohistochemistry using paraformaldehyde-fixed cryosections (Sengupta, A., et al. (2007). J. Histochem. Cytochem. 55(5):525-534).
Immunofluorescence Analysis: A representative lot detected GnRH-I immunoreactivity in frozen mouse hypothalamic sections by fluorescent immunohistochemistry (Olcese, J., et al. (2003). Neuroreport. 14(4):613-618).
Electron Microscopy: A representative lot detected GnRH-I immunoreactivity associated with the luminal epithelium secretory vesicles of rat oviduct by EM using paraformaldehyde-fixed LR wihite sections from rats at day 16 of pregnancy (Sengupta, A., et al. (2007). J. Histochem. Cytochem. 55(5):525-534).
Immunohistochemistry Analysis: A representative lot detected GnRH-I immunoreactivity throughout the hypothalamus in paraformalin-fixed, paraffin-embedded South American plains vizcacha (Lagostomus maximus) brain sections (Dorfman, V.B., et al. (2011). J. Mol. Histol. 42(4):311-321).
Immunohistochemistry Analysis: A representative lot detected GnRH-I-positie neurons in formalin-fixed, paraffin-embedded mouse brain sections (Bergman, J.E., et al. (2010). Eur. J. Hum. Genet. 18(2):171-177).
Immunohistochemistry Analysis: A representative lot detected GnRH-I immunoreactivity in paraformaldehyde-fixed rat brain vibratome sections (Urbanski, H.F., et al. (1991). Biol. Reprod. 44(4):681-686).
Research Category
Neuroscience
Neuroscience
Research Sub Category
Developmental Neuroscience
Developmental Neuroscience
品質
Evaluated by Immunohistochemistry in human prostate tissue.
Immunohistochemistry Analysis: A 1:50 dilution of this antibody detected Gonadotropin-Releasing Hormone in human prostate tissue.
Immunohistochemistry Analysis: A 1:50 dilution of this antibody detected Gonadotropin-Releasing Hormone in human prostate tissue.
標靶描述
10 kDa calculated
外觀
Protein G Purified
Format: Purified
Purified mouse monoclonal IgG1κ antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.
儲存和穩定性
Stable for 1 year at 2-8°C from date of receipt.
其他說明
Concentration: Please refer to lot specific datasheet.
免責聲明
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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儲存類別代碼
12 - Non Combustible Liquids
水污染物質分類（WGK）
WGK 1
閃點（°F）
Not applicable
閃點（°C）
Not applicable
Zixuan Gao et al.
Journal of ovarian research, 13(1), 106-106 (2020-09-15)
The exact pathogenesis of polycystic ovary syndrome (PCOS), the most common neuroendocrine disorder in women of reproductive age, has not been fully elucidated. Recent studies suggested that chronic inflammation and neurotransmitter disorder involved in the progress of PCOS. Troxerutin, a
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