Human U8 snoRNA-Decapping Enzyme (NUDT16) ELISA Kit

Human U8 snoRNA-Decapping Enzyme (NUDT16) ELISA Kit
715€ (96 tests)

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Name
Human U8 snoRNA-Decapping Enzyme (NUDT16) ELISA Kit
Category
ELISA Kits
Provider
Abbexa
Reference
abx381914
Tested Applications
ELISA

Description

Human U8 snoRNA-Decapping Enzyme (NUDT16) ELISA Kit is an ELISA kit against Human U8 snoRNA-Decapping Enzyme (NUDT16) (NUDT16).

Documentos del producto

Instrucciones
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Data sheet
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Especificaciones del producto

Category
ELISA Kits
Immunogen Target
U8 snoRNA-Decapping Enzyme (NUDT16)
Reactivity
Human
Detection Method
Colorimetric
Assay Data
Quantitative
Assay Type
Sandwich
Test Range
0.156 ng/ml - 10 ng/ml
Sensitivity
< 0.06 ng/ml
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Size 1
96 tests
Form
Standard Form: Lyophilized
Tested Applications
ELISA
Sample Type
Tissue homogenates, cell lysates and other biological fluids.
Availability
Shipped within 5-15 working days.
Storage
Shipped at 4°C. Upon receipt, store the kit according to the storage instruction in the kit's manual.
Dry Ice
No
UniProt ID
Q96DE0
Gene ID
131870
OMIM
617381
Background
Elisa Kits for: NUDT16
Status
RUO
Note
This product is for research use only. The range and sensitivity is subject to change. Please contact us for the latest product information. For accurate results, sample concentrations must be diluted to mid-range of the kit. If you require a specific range, please contact us in advance or write your request in your order comments. Please note that our ELISA and CLIA kits are optimised for detection of native samples, rather than recombinant proteins. We are unable to guarantee detection of recombinant proteins, as they may have different sequences or tertiary structures to the native protein.
The stability of the kit is determined by the rate of activity loss. The loss rate is less than 5% within the expiration date under appropriate storage conditions. To minimize performance fluctuations, operation procedures and lab conditions should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same user throughout.

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