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MN (Shorten Name),
Product Name:

General MN/ Mannose ELISA Kit

 
Cat.#:

E1543Ge

Brand:
EIAab®
Regulatory Status:
Detection Method:
ELISA
Assay Type:
Competitive
Detection Range:
1.56-100ng/mL
Sensitivity:
0.37ng/mL
Specificity:
Natural and recombinant general Mannose
Sample Type:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Sample Data:
Assay Procedure:
Research Area:
-
Product Overview:
E1543Ge is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the A Disintegrin and Metalloprotease 30 (Mannose) ELISA Kit target analytes in biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing Mannose. The ELISA analytical biochemical technique of the E1543Ge kit is based on Mannose antibody-Mannose antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect Mannose antigen targets in samples. The ELISA Kit is designed to detect native, recombinant, Mannose. Appropriate sample types may include undiluted human body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).
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Product Datasheets
Datasheet:
Instruction:
MSDS:


Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Mannose and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Sample

1:2

1:4

1:8

1:16

serum(n=5)

86-96%

93-93%

106-116%

94-103%

EDTA plasma(n=5)

110-120%

106-118%

105-113%

98-107%

heparin plasma(n=5)

106-117%

 

103-116%

110-119%

101-101%

 

General Annotation


Sub Unit:
N/A


Function:
Mannose is a sugar monomer of the aldohexose series of carbohydrates. Mannose is a C-2 epimer of glucose. Mannose is important in human metabolism, especially in the glycosylation of certain proteins. Several congenital disorders of glycosylation are associated with mutations in enzymes involved in mannose metabolism.


Location:
N/A


This product has not yet been referenced specifically in any publications.
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