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Key Features

Human TGF-beta ELISA Kit (HUFI00248)

SKU HUFI00248
Product Type ELISA Kit
Size 48T/96T
Reactivity Human
Detection Method Sandwich ELISA, Double Antibody
Sensitivity 18.75 pg/mL
Range 31.25-2000 pg/mL (1pg=25mIU)
€649
Global Shipping: 80+ Countries
White Glove Service: Available upon request
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Distributors: 60+ Countries

Description

Human TGF-beta ELISA Kit

Transforming growth factor beta (TGF-β) is a multifunctional cytokine that plays a critical role in various biological processes, including cell growth, differentiation, and immune regulation. It is part of a superfamily of proteins known for their ability to control cellular functions and influence tissue development. TGF-β is involved in numerous physiological and pathological processes, such as embryogenesis, wound healing, inflammation, and cancer progression. By measuring the levels of TGF-β in biological samples, such as serum or cell culture supernatants, the TGF Beta ELISA kit provides a valuable tool for researchers and clinicians to study the role of TGF-β in disease mechanisms, monitor treatment responses, and explore potential therapeutic interventions.

system_update_alt Datasheet system_update_alt MSDS

Key Features

Save Time Pre-coated 96 well plate
Quick Start Kit includes all necessary reagents
Publication Ready Reproducible and reliable results

Overview

Product Name:

Human TGF-beta ELISA Kit

Product Code:

HUFI00248

Size:

96 Assays

Alias:

TGF-beta1, Transforming Growth Factor Beta 1, TGF-B1, TGFB, TGFbeta, CED, DPD1, TGFbeta1

Detection Method:

Sandwich ELISA, Double Antibody

Application:

This immunoassay kit allows for the in vitro quantitative determination of Human TGF-beta1 concentrations in serum plasma and other biological fluids.

Sensitivity:

18.75pg/ml

Range:

31.25-2000pg/ml

Storage:

4°C for 6 months

Note:

For Research Use Only

Additional Information

Recovery

Matrices listed below were spiked with certain level of Human TGF-beta1 and the recovery rates were calculated by comparing the measured value to the expected amount of Human TGF-beta1 in samples.

Matrix

Recovery Range (%)

Average (%)

serum(n=5)

85-102

95

EDTA plasma(n=5)

96-104

99

UFH plasma(n=5)

92-102

97

Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Human TGF-beta1 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Sample

1:2

1:4

1:8

serum(n=5)

89-95%

89-103%

85-103%

EDTA plasma(n=5)

92-101%

86-101%

86-95%

UFH plasma(n=5)

81-97%

80-99%

85-100%

CV(%)

Intra-Assay: CV<8%
Inter-Assay: CV<10%

Kit Components

Component Quantity Storage

ELISA Microplate (Dismountable)

8x12 strips

4°C for 6 months

Lyophilized Standard

2

4°C/ -20°C

Sample/Standard Dlution Buffer

20ml

4°C

Biotin-labeled Antibody (Concentrated)

120ul

4°C (Protection from light)

Antibody Dilution Buffer

10ml

4°C

HRP-Streptavidin Conjugate (SABC)

120ul

4°C (Protect from light)

SABC Dilution Buffer

10ml

4°C

TMB Substrate

10ml

4°C (Protection from light)

Stop Solution

10ml

4°C

Wash Buffer (25X)

30ml

4°C

Plate Sealer

5

-

Other materials required:

  • Microplate reader with 450 nm wavelength filter
  • Multichannel Pipette, Pipette, microcentrifuge tubes and disposable pipette tips
  • Incubator
  • Deionized or distilled water
  • Absorbent paper
  • Buffer resevoir

Protein Information

Heading 1 Heading 2

UniProt

NCBI GenInfo Identifier

NCBI Gene ID

Molecular Weight

44,341 Da

Protein Family

Transforming growth factor

Protocol

*Note: Protocols are specific to each batch/lot. For the exact instructions please follow the protocol included in your kit.

Before adding to wells, equilibrate the SABC working solution and TMB substrate for at least 30 min at 37°C. When diluting samples and reagents, they must be mixed completely and evenly. It is recommended to plot a standard curve for each test.

Step Procedure

1.

Set standard, test sample and control (zero) wells on the pre-coated plate respectively, and then, record their positions. It is recommended to measure each standard and sample in duplicate. Wash plate 2 times before adding standard, sample and control (zero) wells!

2.

Aliquot 0.1ml standard solutions into the standard wells.

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