Progranulin (human) ELISA Kit (mAb/mAb)

AdipoGen Life Sciences
Product Code: AG-45B-0027
Product Group: ELISA Kits
CodeSizePrice
AG-45B-0027-KI0196 wells£540.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Regulatory Status: RUO
Target Species: Human
Shipping:
BLUE ICE
Storage:
Short Term Storage: +4°C. Long Term Storage: +4°C

Images

1 / 1
Standard Curve

Standard Curve

Further Information

Alternate Names/Synonyms:
Acrogranin; Epithelin Precursor; Glycoprotein of 88 Kda; GP88; Glycoprotein 88; Granulin Precursor; PC Cell-derived Growth Factor; PCDGF; Proepithelin; PEPI
Assay Type:
Sandwich
Detection Type:
Colorimetric
EClass:
32160000
Form (Short):
solid
Handling Advice:
After standard reconstitution, prepare aliquots and store at -20°C. Avoid freeze/thaw cycles. Plate and reagents should reach room temperature before use.
Long Description:
Colorimetric Sandwich ELISA Assay. Detects human progranulin in cell culture supernatants, serum and plasma and allows the detection of Progranulin FTLD mutations. Range: 0.063 to 4ng/ml. Sensitivity: 60pg/ml. Samples: Cell Culture Supernatant, Plasma, Serum. Progranulin (PGRN) is a widely expressed pluripotent growth factor that plays a role in processes such as development, wound repair and inflammation by activating signaling cascades that control cell cycle progression and cell motility. In addition, PGRN has also been linked to tumorigenesis. New cutting-edge publications have shown that progranulin might be a biomarker not only for FTLD but also for other types of Alzheimer?s disease (AD). This new data even suppose the potential of progranulin to be a biomarker for MCI (Mild Cognitive Impairment), which would be a hallmark in AD research. Additionally, PGRN is described as a new ligand of TNF receptors and a potential therapeutic against inflammatory diseases like arthritis. Mutations in PGRN have been found to be a common cause of familial frontotemporal lobar degeneration called FTLD. Since Progranulin has neurotrophic properties and most mutations are predicted to result in a heterozygous loss of gene expression, PGRN deficiency so-called haploinsufficiency is thought to cause neurodegeneration in these patients. GRN mutations are frequent causes of familial frontotemporal degeneration. Reduced progranulin levels in plasma or serum, constitute a reliable, cost-effective biomarker, suitable as a screening tool in patients with familial frontotemporal degeneration. The new mAb-based human Progranulin ELISA Kit has been thor?oughly validated and compared to the standard pAb-based ELISA Kit from AdipoGen (Prod. No. AG-45A-0018Y). With this new ELISA Kit, levels below 50 ng/ml are strongly suggestive of GRN mutations. In a validation on 191 patient samples, confirmed by a molecular gene analysis, the new kit provided a sensitivity and specificity of 100% for de?tecting FTLD mutations.
NCBI, Uniprot Number:
P28799
Package Type:
Box
Product Description:
Progranulin (PGRN) is a widely expressed pluripotent growth factor that plays a role in processes such as development, wound repair and inflammation by activating signaling cascades that control cell cycle progression and cell motility. In addition, PGRN has also been linked to tumorigenesis. New cutting-edge publications have shown that progranulin might be a biomarker not only for FTLD but also for other types of Alzheimer?s disease (AD). This new data even suppose the potential of progranulin to be a biomarker for MCI (Mild Cognitive Impairment), which would be a hallmark in AD research. Additionally, PGRN is described as a new ligand of TNF receptors and a potential therapeutic against inflammatory diseases like arthritis. Mutations in PGRN have been found to be a common cause of familial frontotemporal lobar degeneration called FTLD. Since Progranulin has neurotrophic properties and most mutations are predicted to result in a heterozygous loss of gene expression, PGRN deficiency so-called haploinsufficiency is thought to cause neurodegeneration in these patients. GRN mutations are frequent causes of familial frontotemporal degeneration. Reduced progranulin levels in plasma or serum, constitute a reliable, cost-effective biomarker, suitable as a screening tool in patients with familial frontotemporal degeneration. The new mAb-based human Progranulin ELISA Kit has been thor?oughly validated and compared to the standard pAb-based ELISA Kit from AdipoGen (Prod. No. AG-45A-0018Y). With this new ELISA Kit, levels below 50 ng/ml are strongly suggestive of GRN mutations. In a validation on 191 patient samples, confirmed by a molecular gene analysis, the new kit provided a sensitivity and specificity of 100% for de?tecting FTLD mutations.
Product Line Areas NEW:
Assay, Cancer, Inflammation, Metabolism, Neurobiology, Neurodegenerative Disease
Range:
0.063 to 4ng/ml
Sample Type:
Cell Culture Supernatant, Plasma, Serum
Sensitivity:
60pg/ml
Specificity:
Detects human progranulin in cell culture supernatants, serum and plasma and allows the detection of Progranulin FTLD mutations.
Transportation:
Non-hazardous
UNSPSC Category:
ELISA Kits
UNSPSC Number:
41116126
Use & Stability:
12 months after the day of manufacturing. See expiry date on ELISA Kit box.