Recombinant Human Claudin-6-Nanodisc(Full Length) Protein, Fluorescent at 5 μg/mL (100 μL/well) can bind Anti-Human Claudin6 Antibody, Human IgG1, the EC50 is 8-24 ng/mL.

Claudin-6 Protein, Human, Recombinant (GFP & His) is expressed in HEK293 mammalian cells with GFP and His tag. The predicted molecular weight is 23.3 kDa and the accession number is P56747-1.

Human

HEK293 Cells

claudin 6

A DNA sequence encoding the Human CLDN6(P56747-1) (Met1-Val220) was expressed with a C-terminal GFP followed by a His tag.Nanodisc is a versatile tool for studying membrane proteins. Using styrene-maleic acid (SMA) copolymer, membrane proteins can be extracted directly from prokaryotic and eukaryotic expression systems in the absence of detergents to preserve the protein structure and function better. Compared to membrane scaffold proteins (MSPs) nanodiscs, SMA nanodiscs also have the advantage of preserving proteins' nature by maintaining native lipids surrounded without introducing any heterologous proteins, which allows studies of protein structure and functions in a native-like environment. Predicted N terminal: Met 1

≥ 80 % as determined by SDS-PAGE.

It is recommended to store the product under sterile conditions at -70°C or lower. Samples are stable for up to 3 months at -80°C. Please avoid multiple freeze-thaw cycles and store products in aliquots.

Claudin-6 (CLDN6) belongs to the claudins family and is a transmembrane protein found in tight junctions with two extracellular loops and intracellular N and C tails. CLDN6 modulates the ion- and charge-specific permeability of the paracellular pathway in most epithelial tissues. It regulates the paracellular flux of cations in the kidney through forming heterotypic strands with other claudins and has a role in maintaining the lung epithelial barrier function. The CLDN6 gene is adjacent to another family member, CLDN9, on chromosome 16. Certain CLDN6-positive cancers, encompassing ovarian, endometrial, and testicular malignancies, have been shown to have their proliferation and invasiveness suppressed upon CLDN6 silencing.