2024年12月24日 · BBS5 (Bardet-Biedl Syndrome 5) is a Protein Coding gene. Diseases associated with BBS5 include Bardet-Biedl Syndrome 5 and Bardet-Biedl Syndrome. Among its related pathways are Organelle biogenesis and maintenance and Cargo trafficking to the periciliary membrane.

Bardet–Biedl syndrome 5 protein is a protein that in humans is encoded by the BBS5 gene. [5][6][7] This gene encodes a protein that has been directly linked to Bardet–Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities.

2012年2月13日 · This item can be returned in its original condition for a full refund or replacement within 30 days of receipt. We offer easy, convenient returns with at least one free return option: no shipping charges. All returns must comply with our returns policy. Some of these items ship sooner than the others.

2025年2月8日 · Novel mutations in BBS5 highlight the importance of this gene in non-Caucasian Bardet-Biedl syndrome patients. This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities.

Eaton Bussmann series BBS fuse, 5 A, Non-indicating, Ferrule end x ferrule end, 10 kAIC at 600 Vac, Nickel-plated brass endcaps, Standard, 600 V. Products in your cart cannot be sold together in one transaction. Please choose to either keep your existing cart, or create a …

2024年1月7日 · Clinical resource with information about BBS5, Bardet-Biedl syndrome 5, and available tests. There are links to practice guidelines and authoritative resources like GeneReviews, PubMed, MedlinePlus, PharmGKB and clinicaltrials.gov.

BBS5抗体（B-11）是一种IgG1 κ小鼠单克隆BBS5抗体（也称为BBS5抗体），可通过WB、IP、IF和ELISA检测小鼠、大鼠和人类来源的BBS5蛋白。 BBS5抗体（B-11）既可以是非偶联形式的抗BBS5抗体，也可以是多种偶联形式的抗BBS5抗体，包括琼脂糖、HRP、PE、FITC和多种Alexa Fluor®偶联物。 巴德-比德尔综合征（BBS）是一种多效性遗传性疾病，其特征为肥胖、感光细胞退化、多指（趾）、生殖器发育不全、肾脏异常和发育迟缓。 BBS患者的其他相关临床表现 …

2017年8月25日 · In a consanguineous Turkish family (PB108) with Bardet-Biedl syndrome (BBS5; 615983), Li et al. (2004) identified an insertion-deletion mutation at nucleotide 263 of the BBS5 …

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