Human Growth Differentiation Factor 11 GDF11 ELISA Kit View larger

Human Growth Differentiation Factor 11 GDF11 ELISA Kit

BG-HUM11023

Human Growth Differentiation Factor 11 (Gdf11) ELISA Kit

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$549.00

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Assay Range

31.3 – 2000 pg/mL  

Specificity

No cross-reaction with other related substances detected

Size

96T

Storage

Store at 2 - 8ºC. Keep reconstituted standard and detection Ab at -20 ºC

Assay Principle

Sandwich ELISA

Sample Volume

100 µL final volume, dilution factor varies on samples

Sample Type

serum, plasma, body fluids, tissue lysateor cell culture supernatant 

Detection Method

Chromogenic

 

 

Kit Components

 

 1. Recombinant Human GDF-11 standard: 2 vials

 2. One 96-well plate coated with Human GDF-11  Ab

 3. Sample diluent buffer: 12 mL - 1

 4. Detection antibody: 1 vial, dilution 1:100

 5. Streptavidin-HRP:  1 vial, dilution 1:200

 6. Antibody diluent buffer: 12 mL x1   

 7. Streptavidin-HRP diluent buffer: 12 mL x1

 8. TMB developing agent: 10 mL x1

 9. Stop solution: 10 mL x1

 10. Washing solution (20x): 25 mL x1

 

 

Background

 

GDF11 (Growth differentiation factor 11), also known as bone morphogenetic protein 11 (BMP-11), is a member of transforming growth factor beta superfamily (TGFβ). The mature 109 amino acid (aa) GDF11, derived from the full-length 407 aa GDF11 precursor protein, contains a canonical 7cysteine motif of the TGFβ superfamily members. GDF11 plays a key role in regulating embryonic development. This cytokine inhibits the proliferation of olfactory receptor neuron progenitors to regulate the number of olfactory receptor neurons occurring in the olfactory epithelium, and controls the competence of progenitor cells to regulate numbers of retinal ganglionic cells developing in the retina. Other studies in mice suggest that GDF11 is involved in mesodermal formation and neurogenesis during embryonic development. GDF11 knock-out mice show diverse abnormalities including palatal malformation, vertebral defects, elongated trunks with a reduced or absent tail, missing or malformed kidneys, and an increased number of neurons in the olfactory epithelium.

 

GDF11 has been identified as a blood circulating factor that has the ability to reverse cardiac hypertrophy in mice as a result of hypertrophy related to aging. GDF11 gene expression and protein abundance decreases with age, and it shows differential abundance between young and old mice in parabiosis procedures, causing youthful regeneration of cardiomyocytes, a reduction in the Brain natriuretic peptide (BNP) and in theAtrial natriuretic peptide (ANP).GDF11 also causes an increase in expression of SERCA-2, an enzyme necessary for relaxation during diastolic functions. GDF11 activates the TGF-β pathway in cardiomyocytes derived from pluripotent hematopoietic stem cells and suppresses the phosphorylation of Forkhead (FOX proteins) transcription factors.

 

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