( We provide with GLA qPCR primers for gene expression analysis, HP101606 )
|Vector Type||Mammalian Expression Vector|
|Expression Method||Constiutive, Stable / Transient|
|Selection In Mammalian Cells||Hygromycin|
FLAG-tag, or FLAG octapeptide, is a polypeptide protein tag that can be added to a protein using recombinant DNA technology. It can be used for affinity chromatography, then used to separate recombinant, overexpressed protein from wild-type protein expressed by the host organism. It can also be used in the isolation of protein complexes with multiple subunits.
A FLAG-tag can be used in many different assays that require recognition by an antibody. If there is no antibody against the studied protein, adding a FLAG-tag to this protein allows one to follow the protein with an antibody against the FLAG sequence. Examples are cellular localization studies by immunofluorescence or detection by SDS PAGE protein electrophoresis.
The peptide sequence of the FLAG-tag from the N-terminus to the C-terminus is: DYKDDDDK (1012 Da). It can be used in conjunction with other affinity tags, for example a polyhistidine tag (His-tag), HA-tag or Myc-tag. It can be fused to the C-terminus or the N-terminus of a protein. Some commercially available antibodies (e.g., M1/4E11) recognize the epitope only when it is present at the N-terminus. However, other available antibodies (e.g., M2) are position-insensitive.
|人 alpha-Galactosidase A 基因ORF全长cDNA克隆(表达载体), C-GFPSpark 标签||HG12078-ACG|
|人 alpha-Galactosidase A 基因ORF全长cDNA克隆(表达载体), C-OFPSpark 标签||HG12078-ACR|
|人 alpha-Galactosidase A 基因ORF全长cDNA克隆(表达载体), C-Flag 标签||HG12078-CF|
|人 alpha-Galactosidase A 基因ORF全长cDNA克隆(表达载体), C-His 标签||HG12078-CH|
|人 alpha-Galactosidase A 基因ORF全长cDNA克隆(表达载体), C-Myc 标签||HG12078-CM|
|人 alpha-Galactosidase A 基因ORF全长cDNA克隆(表达载体), C-HA 标签||HG12078-CY|
|人 alpha-Galactosidase A 基因ORF全长cDNA(克隆载体)||HG12078-G|
|人 alpha-Galactosidase A 基因ORF全长cDNA克隆(表达载体), N-Flag 标签||HG12078-NF|
|人 alpha-Galactosidase A 基因ORF全长cDNA克隆(表达载体), N-His 标签||HG12078-NH|
|人 alpha-Galactosidase A 基因ORF全长cDNA克隆(表达载体), N-Myc 标签||HG12078-NM|
|人 alpha-Galactosidase A 基因ORF全长cDNA克隆(表达载体), N-HA 标签||HG12078-NY|
|人 alpha-Galactosidase A 基因ORF全长cDNA克隆(表达载体)||HG12078-UT|
Alpha-galactosidase A, also known as Alpha-D-galactoside galactohydrolase, Alpha-D-galactosidase A, Melibiase and GLA, is a member of the glycosyl hydrolase 27 family. GLA is used as a long-term enzyme replacement therapy in patients with a confirmed diagnosis of Fabry disease. Defects in GLA are the cause of Fabry disease (FD) which is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. The disease consists of an inborn error of glycosphingolipid catabolism. FD patients show systemic accumulation of globotriaoslyceramide (Gb3) and related glycosphingolipids in the plasma and cellular lysosomes throughout the body. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Deficiency of GLA leads to the accumulation of glycosphingolipids in the vasculature leading to multiorgan pathology. In addition to well-described microvascular disease, deficiency of GLA is also characterized by premature macrovascular events such as stroke and possibly myocardial infarction.