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SAR1B Knockout Cell Lines

Gene: SAR1B

Official Full Name: secretion associated Ras related GTPase 1Bprovided by HGNC

Gene Summary: The protein encoded by this gene is a small GTPase that acts as a homodimer. The encoded protein is activated by the guanine nucleotide exchange factor PREB and is involved in protein transport from the endoplasmic reticulum to the Golgi. This protein is part of the COPII coat complex. Defects in this gene are a cause of chylomicron retention disease (CMRD), also known as Anderson disease (ANDD). Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Mar 2010]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO04414 SAR1B Knockout cell line (HeLa) Human SAR1B 1:3~1:6 Negative Online Inquiry
KO04415 SAR1B Knockout cell line (HCT 116) Human SAR1B 1:2~1:4 Negative Online Inquiry
KO04416 SAR1B Knockout cell line (HEK293) Human SAR1B 1:3~1:6 Negative Online Inquiry
KO04417 SAR1B Knockout cell line (A549) Human SAR1B 1:3~1:4 Negative Online Inquiry

Background

SAR1B Gene Knockout Cell Lines are genetically engineered cell models specifically designed to study the function of the SAR1B gene, a crucial component in the intracellular transport of proteins, particularly those entering the secretory pathway. By performing a knockout of the SAR1B gene, these cell lines allow researchers to investigate the consequences of impaired protein trafficking, which can have significant implications in conditions such as congenital disorders and metabolic diseases.

The primary function of the SAR1B gene is to encode a small GTPase that plays a pivotal role in the early secretory pathway, facilitating the transport of proteins from the endoplasmic reticulum to the Golgi apparatus. In SAR1B knockout cell lines, the lack of functional SAR1B leads to disrupted COPII coat formation, resulting in the accumulation of proteins within the endoplasmic reticulum. This modeling is essential for understanding the cellular mechanisms behind various pathologies linked to aberrant protein processing and trafficking.

In research and clinical settings, SAR1B gene knockout cell lines serve as critical tools for unraveling disease mechanisms and testing therapeutic strategies. By providing a platform to simulate conditions related to SAR1B dysfunction, these cell lines can aid in drug discovery, and biological pathway elucidation.

Compared to traditional cell lines, SAR1B knockout models offer substantial advantages, including specificity for the SAR1B gene, reproducibility in experimental outcomes, and the ability to explore personalized medicine approaches. This specificity allows researchers to pinpoint the role of SAR1B in disease models without the confounding effects seen in non-targeted approaches.

For researchers and clinicians seeking to deepen their understanding of protein transport disorders or develop novel therapeutic interventions, SAR1B gene knockout cell lines represent a valuable resource. The unique insights they provide into the cellular and molecular underpinnings of protein trafficking hold promise for advancing both basic and applied biological research.

Our company specializes in providing high-quality biological models tailored for specific research applications, backed by extensive expertise in genetic engineering and cell biology. With a commitment to supporting the scientific community, we ensure our products empower researchers to achieve groundbreaking discoveries.

Please note that all services are for research use only. Not intended for any clinical use.

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