產(chǎn)品編號 | bs-10434R |
英文名稱 | NR0B1 Rabbit pAb |
中文名稱 | 腎上腺發(fā)育不全相關(guān)蛋白抗體 |
別 名 | NR0B1/Dax1; AHC; AHCH; AHX; DAX 1; DAX-1; DAX1; Dosage sensitive sex reversal; DSS; DSS AHC critical region on the X chromosome protein 1; DSS-AHC critical region on the X chromosome protein 1; GTD; HHG; Nr0b1; NR0B1_HUMAN; NROB1; Nuclear hormone receptor; Nuclear receptor 0B1; Nuclear receptor DAX 1; Nuclear receptor DAX-1; Nuclear receptor DAX1; Nuclear receptor subfamily 0 group B member 1; SRXY2. |
研究領(lǐng)域 | 細胞生物 發(fā)育生物學 染色質(zhì)和核信號 神經(jīng)生物學 信號轉(zhuǎn)導 表觀遺傳學 |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應 | (predicted: Human,Mouse,Rat,Rabbit,Pig,Sheep,Cow,Chicken,Horse) |
產(chǎn)品應用 | WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
理論分子量 | 52 kDa |
檢測分子量 | |
細胞定位 | 細胞核 細胞漿 |
性 狀 | Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human NR0B1: 331-430/470 |
亞 型 | IgG |
純化方法 | affinity purified by Protein A |
緩 沖 液 | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
保存條件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
注意事項 | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
PubMed | PubMed |
產(chǎn)品介紹 |
Adrenal hypoplasia congentia (AHC) is an X-linked disorder characterized by primary adrenal insufficiency. The disorder, which is lethal if untreated, results in adrenal insufficiency early in infancy and is characterized by low serum concentration of glucocorticoids, mineralcorticoids and androgens and failure to respond to ACTH. AHC has been mapped to chromosome Xp21 at the same or close to an X-linked locus involved in sex determination, DSS (for dosage-sensitive sex reversal). The gene corresponding to DSS and AHC (designated DAX-1 for DSS-AHC critical region on the X chromosome, gene 1) has been cloned and shown to be deleted in AHC deletion patients and mutated in AHC non-deletion patients. The carboxy terminal 250 amino acids of the DAX-1-encoded protein, DAX-1, exhibits approximately 50% continuous similarity to the ligand-binding domain of the members of the nuclear hormone receptor superfamily while the amino terminal domain contains a putative DNA-binding motif. DAX-1 binds to retinoic acid responsive elements and down regulates retinoic acid receptor-mediated transcriptional activation. Function: Orphan nuclear receptor. Component of a cascade required for the development of the hypothalamic-pituitary-adrenal-gonadal axis. Acts as a coregulatory protein that inhibits the transcriptional activity of other nuclear receptors through heterodimeric interactions. May also have a role in the development of the embryo and in the maintenance of embryonic stem cell pluripotency. Subunit: Homodimer. Interacts with NR5A1, NR5A2, NR0B2 and with COPS2. Subcellular Location: Nucleus. Cytoplasm. Shuttles between the cytoplasm and nucleus. Homodimers exits in the cytoplasm and in the nucleus. DISEASE: Defects in NR0B1 are the cause of X-linked adrenal hypoplasia congenital (XL-AHC) [MIM:300200]; also known as X-linked Addison disease (AHX). XL-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. Defects in NR0B1 are the cause of 46,XY sex reversal type 2 (SRXY2) [MIM:300018]. It is a condition characterized by male-to-female sex reversal in the presence of a normal 46,XY karyotype. Note=XY individuals with a duplication of part of the short arm of the X chromosome and an intact SRY gene develop as females. The single X chromosome in these individuals does not undergo X-chromosome inactivation; therefore, these individuals presumably carry 2 active copies of genes, including the NR0B1 gene, in the duplicated region. Individuals with deletion of this region develop as males. Genes within the dosage-sensitive sex reversal region are, therefore, not essential for testis development, but, when present in a double dose, interfere with testis formation. Similarity: Belongs to the nuclear hormone receptor family. NR0 subfamily. SWISS: P51843 Gene ID: 190 Database links: Entrez Gene: 450140 Chimpanzee Entrez Gene: 190 Human Entrez Gene: 11614 Mouse Omim: 300473 Human SwissProt: Q9BG97 Chimpanzee SwissProt: P51843 Human SwissProt: Q61066 Mouse Unigene: 268490 Human Unigene: 5180 Mouse |
1、抗體溶解方法 | |
2、抗體修復方式 | |
3、常用試劑的配制 | |
4、免疫組化操作步驟 | |
5、免疫組化問題解答 | |
6、Western Blotting 操作步驟 | |
7、Western Blotting 問題解答 | |
8、關(guān)于肽鏈的設計 | |
9、多肽的溶解與保存 | |
10、酶標抗體效價測定程序 | |
| 免费无码婬片AAAA在线观看 | 国产污污视频在线观看 | 91午夜福利视频 | 红桃视频网站一区二区精品 | 午夜大片男女免费观看 | 国产精品久久毛片A片软件爽爽 | A毛片免费精品一区二区三区 | 久久国产乱子伦精品一区二区 | 国产一级婬片AAAAA片口述 | 欧美丰满熟妇BBBBBB禁忌 | 一级少妇精品内射自慰久久久久 | 欧美寡妇一级A片免费视频 91少妇高潮呻吟无码精品 | 国产亚洲av17c入口 | 免费做a爰片77777 | 成免费的crm1688 | 精品国产99久久久久久 | 国产成人无码久久久久毛片朴信惠 | 日本啪啪毛片一区二区 | 97人妻一区二区三区免费 | 老熟妇仑乱一区二区av | 欧美一级黃色A片免费看蜜桃 | 黄色视频免费观看中文 | 国产在线拍偷自揄拍精品 | 蜜臀久久99精品久久久画质超高清 | 免费看亚州1级内射 | ,国产乱人伦无无码视频 | 久久精品人妻一区二区三区宅男必备 | 亚洲成人一区二区三区 | 日本无码人妻波多野结衣杨思敏 | 亚洲一区二区 成人网站戴套 | 苍井空一级婬片A片 | 国产一区波多野结衣 | 在线免费观看黄片视频 | 成人A片高清Aaaaaaa | 无码人妻一区二区三区线花季软件 | 亚洲乱码日产精品BD | 精品人妻一区二区三区蜜桃 | 色情无码片a一区二区 | 欧美人妻少妇精品久久黑人 | 免费 无码吹在线观看 |