Biovision
Human CellExp™ FOLR1, Fc Tag, Human Recombinant
- SKU:
- 26-P1339
- UPC:
- MPN:
- Availability:
- Usually Shipped in 5 Working Days
- Storage Temperature:
- -20°C
- Shipping Conditions:
- Gel Pack
- Shelf Life:
- 12 months
Description
Biomolecule/Target: FOLR1
Synonyms: FOLR1, FBP, FOLR, FOLR-1, Folate-receptor-alpha
Alternates names: FOLR1, FBP, FOLR, FOLR-1, Folate-receptor-alpha
Taglines: Mediates delivery of 5-methyltetrahydrofolate to the interior of cells
Taglines: USA
Country of Animal Origin: USA
NCBI Gene ID #.: 2348
NCBI Gene Symbol: FOLR1
Gene Source: Human
Accession #: P15328
Recombinant: Yes
Source: HEK293 cells
Purity by SDS-PAGE #: ≥95%
Assay: SDS-PAGE
Purity: N/A
Assay #2: N/A
Endotoxin Level: < 1.0 EU per/μg
Activity (Specifications/test method): Measured by its binding ability in a functional ELISA.
Biological activity: Immobilized Folic acid-BSA conjugate at 5 μg/mL (100 μL/well) can bind Human FOLR1, Fc Tag with a linear range of 10-78 ng/mL
Results: N/A
Binding Capacity: Immobilized Folic acid-BSA conjugate at 5 μg/mL (100 μL/well) can bind Human FOLR1, Fc Tag with a linear range of 10-78 ng/mL
Unit Definition: N/A
Molecular Weight: 51.3 kDa
Concentration: N/A
Appearance: Lyophilized
Physical form description: Lyophilized from 0.22 μm filtered solution in PBS, pH 7.4. Normally Mannitol or Trehalose is added as protectants before lyophilization.
Reconstitution Instructions: Reconstitute in sterile deionized water to a concentration of 50 μg/ml.
Background Information: Folate Receptor 1 (FOLR1) also known as Folate receptor alpha, Folate Binding Protein (FBP), FOLR, and is a member of the folate receptor (FOLR) family. Members of this gene family have a high affinity for folic acid and for several reduced folic acid derivatives, and mediate delivery of 5-methyltetrahydrofolate to the interior of cells. Mature FOLR1 is an N-glycosylated protein that is anchored to the cell surface by a GPI linkage. FOLR1 is predominantly expressed on epithelial cells and is dramatically upregulated on many carcinomas. FOLR1 is internalized to the endosomal system where it dissociates from its ligand before recycling to the cell surface. A soluble form of FOLR1 can be proteolytically shed from the cell surface into the serum and breast milk. Defects in FOLR1 are the cause of neurodegeneration due to cerebral folate transport deficiency (NCFTD). NCFTD is an autosomal recessive disorder resulting from brain-specific folate deficiency early in life.
Amino acid sequence: N/A
Handling: Centrifuge the vial prior to opening.
Usage: For Research Use Only! Not to be used in humans
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