產(chǎn)品編號 | bs-14412R |
英文名稱 | DPAGT1 Rabbit pAb |
中文名稱 | DPAGT1蛋白抗體 |
別 名 | AU021132; Dolichyl phosphate(UDP N acetylglucosamine) acetylglucosaminephosphotransferase 1(GlcNAc 1 P transferase); DPAGT1; DPAGT2; G1PT; GlcNAc-1-P transferase; Gnpta; GPT; GPT_HUMAN; H2afx; N-acetylglucosamine-1-phosphate transferase; UDP-N-acetylgluco |
![]() |
Specific References (1) | bs-14412R has been referenced in 1 publications.
[IF=6.706] Min Fu. et al. Mechanisms of Sodium/Iodide Symporter-Mediated Mammary Gland Iodine Compensation during Lactation. NUTRIENTS. 2022 Jan;14(17):3592 WB ; Rat.
|
研究領(lǐng)域 | 細胞生物 免疫學(xué) 神經(jīng)生物學(xué) 細胞分化 |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應(yīng) | Human,Mouse,Rat (predicted: Rabbit,Pig,Sheep,Cow,Chicken,Dog,Horse) |
產(chǎn)品應(yīng)用 | WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
理論分子量 | 46 kDa |
檢測分子量 | |
細胞定位 | 細胞漿 |
性 狀 | Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human DPAGT1: 301-408/408 |
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 |
The protein encoded by this gene is an enzyme that catalyzes the first step in the dolichol-linked oligosaccharide pathway for glycoprotein biosynthesis. This enzyme belongs to the glycosyltransferase family 4. This protein is an integral membrane protein of the endoplasmic reticulum. The congenital disorder of glycosylation type Ij is caused by mutation in the gene encoding this enzyme. [provided by RefSeq, Jul 2008] Function: Catalyzes the initial step in the synthesis of dolichol-P-P-oligosaccharides. Subcellular Location: Endoplasmic reticulum membrane. DISEASE: Defects in DPAGT1 are the cause of congenital disorder of glycosylation type 1J (CDG1J) [MIM:608093]. CDGs are a family of severe inherited diseases caused by a defect in protein N-glycosylation. They are characterized by under-glycosylated serum proteins. These multisystem disorders present with a wide variety of clinical features, such as disorders of the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions. Similarity: Belongs to the glycosyltransferase 4 family. SWISS: Q9H3H5 Gene ID: 1798 Database links: Entrez Gene: 1798 Human Entrez Gene: 13478 Mouse Omim: 191350 Human SwissProt: Q9H3H5 Human SwissProt: P42867 Mouse Unigene: 524081 Human Unigene: 18353 Mouse |
產(chǎn)品圖片 |
Protein: lung(mouse) lysate at 40ug;
Primary: rabbit Anti-DPAGT1 (bs-14412R) at 1:300;
Secondary: HRP conjugated Goat-Anti-rabbit IgG(bs-0295G-HRP) at 1: 5000;
Predicted band size: 46 kD
Observed band size: 46 kD
Tissue/cell: Rat brain tissue; 4% Paraformaldehyde-fixed and paraffin-embedded;
Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min;
Incubation: Anti-DPAGT1 Polyclonal Antibody, Unconjugated(bs-14412R) 1:500, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining
Paraformaldehyde-fixed, paraffin embedded (Human kidney); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (DPAGT1) Polyclonal Antibody, Unconjugated (bs-14412R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
|
| 中文字幕无码永久无线无码蜜桃视频 | 国产一级毛片在线视频 | 免费 无码 国产在线 | 国产亚洲分享在播放 | 欧美69久成人做爰视频 | 精品国婬伦v无码久久久黑人 | 少妇做受XXXXⅩ高潮片直播 | 亚洲AV无码乱码A片秀色直播 | 少妇全程高潮喷水WWW久久 | 国产精品视频在线观看 | 国产美女裸体无遮挡网站 | 激情综合五月丁香狠狠爱 | 一级A片迷奷系列迷奷犯 | 色欲AV国产精品无天美 | 天天躁日日躁AAAAXXXX | 国产真人做满A片免费 | 人人操人人爱人人爽 | 成人乱妇无码AV在线 | 人伦人与牲囗恔配视频 | 丰满的已婚人妻中文字幕A片 | 久久久久无码精品国产sm果冻 | 亚洲另类色综合网站 | 在线观看黄www免费视频 | 羞羞视频在线观看免费视频 | 熟女毛多熟妇人妻中出 | 日本国产成人亚洲精品无码 | 成人羞羞 国产免费动态 | 精品人一区二区三区伦蜜桃免费 | 夜夜躁狠狠躁日日躁av | 激情婬妇A片AAA毛多水多麻豆 | 日本人做爰毛片免费播 | 国产免费AV片在线无码免费看 | 无码在线免费视频 | 国产人妻无套一区二区普通话对白 | 91精产国品一二三产区蜜臀 | 亚洲黄色视频XXXX | 久久国产精品无码 | 中文字幕乱码人妻二区三区 | 人妻体体内射精一区二区 | 欧美丰满一区二区免费视频 |