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- Target See all MLC1 products
- MLC1
- Protein Type
- Synthetic Nanodisc
- Origin
- Human
- Source
- HEK-293 Cells
- Purpose
- Human MLC1 full length protein-synthetic nanodisc
- Characteristics
- Unlike other membrane scaffold protein (MSP) Nanodisc on the market, our synthetic Nanodisc can be prepared directly from the cells. The polymers used during this process have a dual function. It dissolves the cell membranes, like the detergent, and uses cellular phospholipids to form Nanodisc around the membrane proteins. The target protein embedded Nanodiscs can then be purified.
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- Comment
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Advantages of Synthetic Nanodiscs:
- Highly purified membrane proteins
- High solubility in aqueous solutions
- High stability
- Proteins are in a native membrane environment and remain biologically active
- No detergent and can be used for cell-based assays
- No MSP backbone proteins
- Intolerant to acids and high concentrations of divalent metal ions
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Buffer
- Lyophilized from nanodisc solubilization buffer (20 mM Tris-HCl, 150 mM NaCl, pH 8.0). Normally 5 % - 8 % trehalose is added as protectants before lyophilization.
- Storage
- -20 °C,-80 °C
- Storage Comment
- Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.
- Expiry Date
- 12 months
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- Target
- MLC1
- Abstract
- MLC1 Products
- Synonyms
- LVM Protein, MLC Protein, VL Protein, AW048630 Protein, BB074274 Protein, Kiaa0027-hp Protein, WKL1 Protein, mKIAA0027 Protein, si:ch211-192n14.1 Protein, megalencephalic leukoencephalopathy with subcortical cysts 1 Protein, megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) Protein, MLC1 Protein, Mlc1 Protein, mlc1 Protein
- Background
- The function of this protein is unknown, however, homology to other proteins suggests that it may be an integral membrane transporter. Mutations in this gene have been associated with megalencephalic leukoencephalopathy with subcortical cysts, an autosomal recessive neurological disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.
- Molecular Weight
- The human full length MLC1 protein has a MW of 41.2 kDa
- UniProt
- Q15049
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