Gene: BIN1
Official Full Name: bridging integrator 1provided by HGNC
Gene Summary: This gene encodes several isoforms of a nucleocytoplasmic adaptor protein, one of which was initially identified as a MYC-interacting protein with features of a tumor suppressor. Isoforms that are expressed in the central nervous system may be involved in synaptic vesicle endocytosis and may interact with dynamin, synaptojanin, endophilin, and clathrin. Isoforms that are expressed in muscle and ubiquitously expressed isoforms localize to the cytoplasm and nucleus and activate a caspase-independent apoptotic process. Studies in mouse suggest that this gene plays an important role in cardiac muscle development. Alternate splicing of the gene results in several transcript variants encoding different isoforms. Aberrant splice variants expressed in tumor cell lines have also been described. [provided by RefSeq, Mar 2016]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO05907 | BIN1 Knockout cell line (HeLa) | Human | BIN1 | 1:3~1:6 | Negative | Online Inquiry |
KO05908 | BIN1 Knockout cell line (HCT 116) | Human | BIN1 | 1:2~1:4 | Negative | Online Inquiry |
KO05909 | BIN1 Knockout cell line (HEK293) | Human | BIN1 | 1:3~1:6 | Negative | Online Inquiry |
KO05910 | BIN1 Knockout cell line (A549) | Human | BIN1 | 1:3~1:4 | Negative | Online Inquiry |
BIN1 Gene Knockout Cell Lines are specialized cellular models developed to investigate the biological functions and contributions of the BIN1 gene, which is critical in cellular processes such as membrane trafficking, endocytosis, and the regulation of cell morphology. By utilizing techniques like CRISPR-Cas9 gene editing, these knockout cell lines effectively diminish or eliminate BIN1 expression, allowing researchers to elucidate the gene's role in cellular dynamics and pathophysiological conditions.
The primary function of the BIN1 Gene Knockout Cell Lines is to serve as powerful tools for studying the mechanisms by which the BIN1 protein influences various cellular pathways. This is especially pertinent in the context of diseases where BIN1 has been implicated, such as cancer, neurodegenerative disorders, and heart conditions. By creating a genetic model that lacks BIN1, researchers can assess the resulting phenotypic changes, enabling them to draw correlations between BIN1 deficiency and disease progression.
Scientifically, these knockout cell lines are invaluable, offering insights into the fundamental aspects of cellular biology and potential therapeutic targets. They can be utilized in various applications, including drug discovery, functional genomics studies, and mechanistic investigations into disease models. Moreover, the use of these specific cell lines enhances reproducibility and reliability in research findings, as they provide a stable background on which experimental variables can be assessed.
Compared to alternative models, BIN1 Gene Knockout Cell Lines hold distinct advantages. The precision of CRISPR-Cas9 technology ensures high efficiency and specificity, minimizing off-target effects that can compromise experimental integrity. Additionally, these cell lines come with thorough validation and characterization, providing researchers with assurance regarding the functional loss of BIN1.
For researchers and clinicians looking to enhance their understanding of BIN1's biological implications, these knockout cell lines offer a unique opportunity to elucidate complex molecular mechanisms. They empower scientific inquiry by enabling more accurate modeling of human diseases and could thus contribute to future therapeutic strategies.
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