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Human Granulin/GRN enzyme immunoassay Kit

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Product Details

Standard - EK1184.jpg


Brand

MultiSciences

Cat Num

70-EK1184

Product Name

Human Granulin/GRN ELISA Kit

Customs Name

Human Granulin/GRN ELISA Kit

Application

ELISA

Reactivity

Human

Assay Type

Sandwich ELISA

Suitable Sample Type

serum, plasma, cell culture supernates

Format

96-well strip plate

Storage

4℃ (unopened)standard stored at -20℃, others stored at 4℃ (opened)

Shipping Condition

4℃

Sample Volume

100 μl (prediluted)

Sensitivity

10.81 pg/ml

Standard Curve Range

125 - 8000 pg/ml

Spike Recovery Range

92 % - 135 %

Mean Spike Recovery

1.04

CV of Intra plate

3.3 % - 4.3 %

CV of Inter plate

3.9 % - 4.8 %

Components

96-well polystyrene microplate coated with a monoclonal antibody against GRN
Human GRN Standard, lyophilized
GRN Detect Antibody
Assay Buffer (10×)
Substrate (TMB)
Stop Solution
Washing Buffer (20×)
Plate Covers

Describtion

This assay employs the quantitative sandwich enzyme immunoassay technique for the quantitative detection of human GRN. The Human Granulin/GRN ELISA is for research use only. Not for diagnostic or therapeutic procedures.
Granulin is a protein that in humans is encoded by the GRN gene. The precursor protein, progranulin, is also called PC cell-derived growth factor. Cleavage of the signal peptide produces mature granulin which can be further cleaved into a variety of active, 6 kDa peptides. Both the peptides and intact granulin protein regulate cell growth. However, different members of the granulin protein family may act as inhibitors, stimulators, or have dual actions on cell growth. Granulin family members are important in normal development, wound healing, and tumorigenesis. Granulins have possible cytokine-like activity. They may play a role in inflammation, wound repair, and tissue remodeling.
The human liver fluke contributes to the development of bile duct (liver) cancer by secreting a granulin-like growth hormone. Mutations in the GRN gene have been implicated in up to 25% of frontotemporal lobar degeneration, inherited in an autosomal dominant fashion with high penetrance.

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