
BbsI - NEB
BbsI has a High Fidelity version BbsI-HF ® (NEB #R3539). High Fidelity (HF) Restriction Enzymes have 100% activity in rCutSmart Buffer; single-buffer simplicity means more straightforward and streamlined sample processing. HF enzymes also exhibit dramatically reduced star activity.
BpiI (BbsI) (10 U/μL) - 赛默飞世尔科技公司
Thermo Scientific BpiI (BbsI) 是一种识别GAAGAC (2/6)^位点并在37C G缓冲液中最佳切割的限制酶。 赛默飞提供的传统限制内切酶是一个高质量的大型集合。 了解更多信息,请访问赛默飞中国官网或联系我们的客服。
BBS1 gene - MedlinePlus
The BBS1 gene provides instructions for making a protein found in cells throughout the body. The BBS1 protein is part of a group (complex) of proteins that plays a critical role in the formation of cell structures called cilia. Cilia are microscopic, finger-like projections that stick out from the surface of many types of cells.
BBS1 Gene - GeneCards | BBS1 Protein | BBS1 Antibody
Mar 28, 2025 · BBS1 (Bardet-Biedl Syndrome 1) is a Protein Coding gene. Diseases associated with BBS1 include Bardet-Biedl Syndrome 1 and Bardet-Biedl Syndrome. Among its related pathways are Organelle biogenesis and maintenance …
BBS1 - Wikipedia
Bardet–Biedl syndrome 1 protein is a protein that in humans is encoded by the BBS1 gene. [5] [6] [7] BBS1 is part of the BBSome complex, which required for ciliogenesis. Mutations in this gene have been observed in patients with the major form (type 1) of Bardet–Biedl syndrome.
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Entry - #209900 - BARDET-BIEDL SYNDROME 1; BBS1 - OMIM
Bardet-Biedl syndrome is an autosomal recessive and genetically heterogeneous ciliopathy characterized by retinitis pigmentosa, obesity, kidney dysfunction, polydactyly, behavioral dysfunction, and hypogonadism (summary by Beales et al., 1999).
Bardet-Biedl Syndrome - Symptoms, Causes, Treatment | NORD
Jul 12, 2022 · Bardet-Biedl syndrome (BBS) is a genetic condition that impacts multiple body systems. It is classically defined by six features. Patients with BBS can experience problems with obesity, specifically with fat deposition along the abdomen. …
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