Bscl2抗体

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August undefined, 2024

http://genetics.cas.cn/dtxw/kyjz/202411/t20241123_6553958.html WebDescription: Homo sapiens BSCL2 lipid droplet biogenesis associated, seipin (BSCL2), transcript variant 1, mRNA. (from RefSeq NM_001122955) RefSeq Summary (NM_001122955): This gene encodes the multi-pass transmembrane protein protein seipin. This protein localizes to the endoplasmic reticulum and may be important for lipid droplet …

Adipose specific disruption of seipin causes early-onset ... - PubMed

WebMar 25, 2024 · 应用: 免疫印迹, 免疫组化, 免疫组化-石蜡切片. Western blot analysis of BSCL2 in NCI-H460 cell line lysates using 35ug per lane of antibody. Immunohistochemical analysis in formalin fixed and paraffin embedded human testis carcinoma followed by peroxidase conjugation of the secondary antibody and DAB staining. 规格: 400微升 ... WebThe more severe form, designated BSCL2, arises due to mutations in the BSCL2 gene. Patients with BSCL2, as well as Bscl2 -/-mice, have a near total absence of body fat, an organomegaly, and develop metabolic disorders including insulin resistance and hepatic steatosis. The function of the Seipin (BSCL2) protein remains poorly understood. h pylori infection is it contagious

Entry - *606158 - BSCL2 GENE; BSCL2 - OMIM

http://www.biofeng.com/gene/renyuan/BSCL2.html WebDec 6, 2005 · BSCL2-related neurologic disorders are inherited in an autosomal dominant manner. Each child of an individual with a BSCL2-related neurologic disorder has a 50% chance of inheriting the … http://www.labome.cn/gene/human/BSCL2-antibody.html h pylori left untreated

Anti-BCL-2 Antibodies Invitrogen - Thermo Fisher

WebNov 23, 2024 · II 型脂肪代谢障碍症是由 BSCL2/seipin 基因突变导致的，是所有脂肪代谢障碍症中最严重的一种类型，病人几乎失去所有的皮下脂肪组织。 Seipin 是一个内质网蛋白，在脂滴稳态和脂质储存的调控中发挥重要的作用。 WebBSCL2/Seipin 在几类人疾病细胞中突变，包括 Berardinelli-Seip 先天性脂质营养不良，这是一种常染色体隐性遗传病，表现为几乎没有脂肪组织、严重胰岛素耐受性、高甘油三酯 … h pylori is it a parasiteWebBCL-2 Antibodies. Antibodies that detect BCL-2 can be used in several scientific applications, including Immunohistochemistry, Western Blot, Immunocytochemistry, Flow … h pylori load therapy

"WebBSCL2/Seipin contains a number of potential glycosylation sites (SwissProt) which may explain its migration at a higher molecular weight than predicted. Western blot - Anti … " - Bscl2抗体

Bscl2抗体

Bcl-2 Antibody Cell Signaling Technology

WebBSCL2 抗体: 货号: DF13508: 来源: Rabbit: 应用: WB, IF/ICC, ELISA(peptide) 反应: Human, Mouse, Rat: 预测: Horse, Rabbit, Dog: 分子量: 44kD; 44kD(Calculated). 蛋白号: … • Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298. • Andersson B, Wentland MA, Ricafrente JY, et al. (1996). "A "double adaptor" method for improved shotgun library construction". Anal. Biochem. 236 (1): 107–13. doi:10.1006/abio.1996.0138. PMID 8619474.

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http://www.labome.cn/gene/human/BSCL2-antibody.html WebObjective: Mutations to the BSCL2 gene disrupt the protein seipin and cause the most severe form of congenital generalised lipodystrophy (CGL). Affected individuals exhibit a near complete loss of white adipose tissue (WAT) and suffer from metabolic disease. Seipin is critical for adipocyte development in culture and mice with germline disruption to Bscl2 …

WebBSCL2 抗体. (Berardinelli-Seip Congenital Lipodystrophy 2 (Seipin) (BSCL2)) This gene encodes the multi-pass transmembrane protein protein seipin. This protein localizes to … WebBSCL2: 基因又名: GNG3LG; HMN5; HMN5C; PELD; SPG17: Gene ID: 26580: 种属: Homo sapiens: DNA序列编号: NM_001122955.4: DNA描述: Homo sapiens BSCL2 lipid droplet …

WebBSCL2 antibody; BSCL2_HUMAN antibody; GNG3LG antibody; HMN 5 antibody; HMN5 antibody; MGC4694 antibody; Seipin antibody; Spastic paraplegia 17 (autosomal … WebMutations in BSCL2/seipin cause Berardinelli-Seip congenital lipodystrophy (BSCL), a rare recessive disorder characterized by near absence of adipose tissue and severe insulin resistance. Since the discovery of the gene in 2001, several cellular studies intended to unravel the biological function of …

Web如果本抗体用于Western blot (WB)、免疫荧光(IF)、免疫细胞化学(ICC)等实验，请注意回收使用过的稀释抗体。回收的抗体通常至少可以重复使用5-10次。稀释后的抗体，包括已经使用过的稀释抗体，请4℃保存。回收后重复使用的抗体，使用方法同新鲜稀释的抗体。

Web【Bcl-2家族蛋白】 Bcl-2是一个进化相关蛋白家族。这些蛋白质控制线粒体外膜通透性（MOMP），可以是促凋亡（Bax、Bad、Bak和Bok等）或抗凋亡（包括Bcl-2 proper、Bcl-xl和Bcl-w等）。目前已知的Bcl-2家族共有25个… h pylori iv therapyWebMar 5, 2024 · This missense change has been observed in individuals with autosomal dominant BSCL2-related conditions (PMID: 14981520, 15732094, 16427281, 20598714, 23553728, 25219579, 25454168). It has also been observed to segregate with disease in related individuals. h pylori locationWebAll lanes : Anti-BSCL2/Seipin antibody (ab106793) at 1 µg/ml Lane 1 : Human brain tissue lysate - total protein Lane 2 : Brain (Mouse) Tissue Lysate Lane 3 : Brain (Rat) Tissue Lysate Lane 4 : Testis (Mouse) Tissue Lysate Lane 5 : Testis (Rat) Tissue Lysate Lysates/proteins at 10 µg per lane. Secondary All lanes : Goat Anti-Rabbit IgG H&L … h pylori long term effectsWebBSCL2抗体详情 (hide) BSCL2 (Berardinelli-Seip Congenital Lipodystrophy 2 (Seipin) (BSCL2)) Immunohistochemistry (IHC), Immunohistochemistry (Paraffin-embedded … h pylori metronidazole clarithromycinWebJun 12, 2024 · Bcl-2 单克隆抗体. BCL2编码一种完整的外部线粒体膜蛋白，可以阻止淋巴细胞等细胞的凋亡死亡。. BCL2的组成性表达，如BCL2易位到Ig重链位点，被认为是卵泡 … h pylori meal planWebDefects in BSCL2 are the cause of congenital generalized lipodystrophy type 2 (CGL2) [MIM:269700]. Congenital generalized lipodystrophy is an autosomal recessive disorder characterized by a near absence of adipose tissue, extreme insulin resistance, hypertriglyceridemia, hepatic steatosis and early onset of diabetes. h pylori mouthwashWeb抗体. 寡核苷酸、引物、探针 ... Impaired adipogenic capacity in induced pluripotent stem cells from lipodystrophic patients with BSCL2 mutations. Metabolism: clinical and experimental. Mori E,Fujikura J,Noguchi M,Nakao K,Matsubara M,Sone M,Taura D,Kusakabe T,Ebihara K,Tanaka T,Hosoda K,Takahashi K,Asaka I,Inagaki N,Nakao K. h pylori location in stomach