Recombinant Human ILDR2 Protein
Beta LifeScience
SKU/CAT #: BLK-01870P-100UG

Human ILDR2 on Tris-Bis PAGE under reduced condition. The purity is greater than 95%.
Recombinant Human ILDR2 Protein
Beta LifeScience
SKU/CAT #: BLK-01870P-100UG
Our products are highly customizable to meet your specific needs. You can choose options such as endotoxin removal, liquid or lyophilized forms, preferred tags, and the desired functional sequence range for proteins. Submitting a written inquiry expedites the quoting process.
Product Overview
Description | Recombinant Human ILDR2 Protein is expressed from HEK293 with hFc tag at the C-Terminus.It contains Leu21-Met184. |
Purity | > 95% as determined by Tris-Bis PAGE;> 92% as determined by HPLC |
Accession | Q71H61 |
Target Symbol | ILDR2 |
Synonyms | ILDR2; C1orf32; dJ782G3.1; RP4-782G3.2 |
Species | Human |
Expression System | HEK293 |
Tag | C-hFc |
Expression Range | Leu21-Met184 |
Mol. Weight | The protein has a predicted MW of 35 kDa. Due to glycosylation, the protein migrates to 48-55 kDa based on Tris-Bis PAGE result. |
Form | Lyophilized |
Formulation | Lyophilized from 0.22um filtered solution in PBS (pH 7.4). Normally 8% trehalose is added as protectant before lyophilization. |
Endotoxin | Less than 1EU per ug by the LAL method. |
Storage | Reconstituted protein stable at -80°C for 12 months, 4°C for 1 week. Use a manual defrost freezer and avoid repeated freeze-thaw cycles. |
Shipping | Shipped at ambient temperature. |
Gene Background | Ildr2, a modifier of diabetes susceptibility in obese mice, is expressed in most organs, including islets and hypothalamus, with reduced levels in livers of diabetes-susceptible B6.DBA mice congenic for a 1.8 Mb interval of Chromosome 1. In hepatoma and neuronal cells, ILDR2 is primarily located in the endoplasmic reticulum membrane. Livers in knockdown mice were steatotic, with increased hepatic and circulating triglycerides and total cholesterol. Increased circulating VLDL, without reduction in triglyceride clearance suggests an effect of reduced hepatic ILDR2 on hepatic cholesterol clearance. |