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Human hepatocyte growth factor,HGF ELISA kit

Product#: CS-CSB-E04573h
$626.80
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Human ELISA Kit · Cancer

Human hepatocyte growth factor,HGF ELISA kit

Sandwich quantitative immunoassay for hepatocyte growth factor (hepapoietin A; scatter factor) in human serum, plasma, tissue homogenates  available in multiple catalog sizes:

Trial 24T 96T

Note: Please send inquiries regarding Trial 24T orders to support@diagnocine.com.

Detection Range
15.6-1,000 pg/mL
Sensitivity
3.9 pg/mL
Assay Time
1-5 hours
Sample Volume
50-100 μL
Product specifications
Target namehepatocyte growth factor (hepapoietin A; scatter factor)
Uniprot No.P14210
SpeciesHomo sapiens (Human)
Sample typesserum, plasma, tissue homogenates
Detection range15.6 pg/mL-1000 pg/mL
Sensitivity3.9 pg/mL
Assay time1-5h
Sample loading volume50-100μL
Detection wavelength450 nm
Assay principleSandwich (Quantitative)
Data analysisStandard curve + Curve Expert software
Research areaCancer
Storage condition2-8°C (see protocol for full details)
Shipping condition4 °C
Shelf life6 months
hepatocyte growth factor (hepapoietin A; scatter factor) serum plasma tissue homogenates Cancer Human ELISA
Lead Time

10 business days

Processing + 3-5 days shipping

Availability

In Stock : USA

Worldwide shipping available

Assay principle
Sample prep
Antibody capture
450 nm detection
Standard curve
Quantification

In this sandwich ELISA, hepatocyte growth factor (hepapoietin A; scatter factor) in the sample is captured between a pre-coated capture antibody and a detection antibody. Signal intensity is proportional to analyte concentration. Quantification uses a standard curve fitted with Curve Expert software, covering 15.6 pg/mL-1000 pg/mL with a minimum detectable dose of 3.9 pg/mL.

For research use only (RUO). Not intended for diagnostic or therapeutic purposes. Validated in human serum, plasma, tissue homogenates matrices only.
Description

The human HGF ELISA kit (CSB-E04573h) is designed for the quantitative measurement of human HGF protein in serum, plasma, or tissue homogenates. It quantitates human HGF with 3.9 pg/ml sensitivity and shows excellent specificity for human HGF. It uses the bi-antibody sandwich enzyme immunoassay technique. This assay employs a biotin-conjugated HGF antibody that recognizes the analyte bound by the immobilized HGF antibody, forming an antibody-analyte-antibody complex. The immune complex is further detected by avidin-conjugated HRP. The TMB solution is added into the wells and turns blue and finally turns yellow after the addition of the stop solution. Solution color develops in proportion to the amount of HGF in the sample. The O.D. value is measured using a microplate reader at 450 nm and is used to determine the concentration of the human HGF in the sample. HGF is a cytokine with pleiotropic functions during wound healing and repair. In the bleomycin model of lung fibrosis, HGF was demonstrated to exert anti-fibrotic effects and associated with improved survival and proliferation of epithelial cells and reduction of myofibroblast accumulation. HGF can induce epithelial-mesenchymal conversion of epithelial cells in culture, with the dissociated cells becoming highly motile. HGF/c-Met signaling pathway has been involved in different processes including development, organ regeneration, and cancer as well as in medulloblastoma pathogenesis.

Alternative Names
DFNB39 ELISA Kit; F TCF ELISA Kit; Fibroblast derived tumor cytotoxic factor ELISA Kit; Hepatocyte growth factor (hepapoietin A; scatter factor) ELISA Kit; Hepatocyte growth factor ELISA Kit; Hepatocyte growth factor beta chain ELISA Kit; Hepatocyte growth factor precursor ELISA Kit; Hepatopoietin A ELISA Kit; Hepatopoietin-A ELISA Kit; Hgf ELISA Kit; HGF_HUMAN ELISA Kit; HGFB ELISA Kit; HPTA ELISA Kit; Lung fibroblast derived mitogen ELISA Kit; OTTHUMP00000161349 ELISA Kit; OTTHUMP00000206710 ELISA Kit; OTTHUMP00000206711 ELISA Kit; OTTHUMP00000206712 ELISA Kit; OTTHUMP00000206713 ELISA Kit; OTTHUMP00000206730 ELISA Kit; Scatter factor ELISA Kit; SF ELISA Kit
Function
Potent mitogen for mature parenchymal hepatocyte cells, seems to be a hepatotrophic factor, and acts as a growth factor for a broad spectrum of tissues and cell types. Activating ligand for the receptor tyrosine kinase MET by binding to it and promoting its dimerization.
Gene References into Functions
  1. Lymph node metastasis is strongly associated with expression status of HGF and CD133 at the deep invasive front, suggesting the usefulness of these proteins as independent predictive markers of lymph node metastasis in early gastric cancer. PMID: 28595915
  2. In summary, a decrease in VEGF-A and an increase in sVEGFR1 during chemotherapy and bevacizumab exposure can contribute to both chemotherapy (due to c-MET/b-catenin activation) and bevacizumab (due to low VEGF requirements) resistance. Because HGF levels decrease also during acquired resistance, alternative strategies to HGF-ligand inhibition should be investigated PMID: 28621236
  3. Oxidative stress contributes to HGF-dependent pro-senescence activity of ovarian cancer cells. PMID: 28652056
  4. this study shows that decidual NK cells facilitate the interaction between trophoblastic and endothelial cells via VEGF-C and HGF PMID: 28653669
  5. miR-26a/mir-26b could suppress tumorigenesis and angiogenesis by targeting the HGF-VEGF axis, and could serve as a potential treatment modality for targeted therapy in the clinical treatment of gastric cancer. PMID: 28738343
  6. These data suggest that paxillin appears to influence major cell functions in a diverse range of prostate and breast cancer models. The responsiveness of cells to environmental factors such as HGF or BME may be influenced by paxillin status, although this seems to be dependent on cell type PMID: 28739717
  7. High glucose activated Met receptor in HK2 cells independently of HGF, via induction of integrin a5b1 and downstream signaling. This mode of Met activation was associated with tubular cell damage and apoptosis and it may represent a novel pathogenic mechanism and a treatment target in diabetic nephropathy. PMID: 28819999
  8. Reduction of fibroblast size upregulates HGF expression, which in turn contributes to loss of collagen, a prominent feature of aged skin. PMID: 28826691
  9. Results of our present study suggest that both IL-6 and HGF derived from Cancer-associated fibroblasts (CAFs)could contribute to the intratumoral androgen metabolism in ER-negative breast carcinoma patients. PMID: 28831645
  10. We also propose that full-length HGF and HGF-NK1 convey desirable wound healing properties, whilst fibroblasts preferentially expressing more HGF-NK2 readily undergo TGF-beta-driven differentiation into myofibroblasts. PMID: 28837064
  11. prolonged treatment of single HGF/c-Met or Hh inhibitor leads to resistance to these single inhibitors, likely because the single c-Met treatment leads to enhanced expression of Shh, and vice versa. Targeting both the HGF/c-Met and Hh pathways simultaneously overcame the resistance to the single-inhibitor treatment and led to a more potent antitumor effect in combination with the chemotherapy treatment. PMID: 28864680
  12. We identify HGF, acting through the c-Met receptor, as the key polarity-inducing morphogen, which acts to activate b1-integrin-dependent adhesion. HGF and ECM-derived integrin signals co-operate via a c-Src-dependent inhibition of the RhoA-ROCK1 signalling pathway via p190A RhoGAP. PMID: 28888686
  13. EGF-mediated lysosome trafficking, protease secretion, and invasion is regulated by the activity of p38 mitogen activated protein kinase (MAPK) and sodium hydrogen exchangers (NHEs). Interestingly, EGF stimulates anterograde lysosome trafficking through a different mechanism than previously reported for HGF, suggesting that there are redundant signaling pathways that control lysosome positioning PMID: 28978320
  14. a higher HGF serum level during hemodialysis treatment is associated with a slower loss of residual renal function PMID: 29227979
  15. TGF-beta negatively controls the HGF/c-MET pathway by regulating of stemness in glioblastoma. PMID: 29238047
  16. widely stained in sclerosing stromal tumours of the ovary PMID: 29433373
  17. These results suggest that gastric cancer progression is not associated with a unique signaling pathway and that a feedback loop may exist between the HGF/c-Met and Notch1 signaling pathways, which may result in therapeutic resistance. PMID: 29781036
  18. This novel study, in HIV-positive, preeclampsia, and normotensive pregnancies, demonstrates that HGF was two-fold higher in conducting compared to exchange villi irrespective of the pregnancy type. HIV infection does not influence HGF expression within the conducting and exchange villi. PMID: 29886319
  19. CAFderived HGF promotes angiogenesis. PMID: 29917165
  20. miR-449a suppresses hepatocellular carcinoma tumorigenesis by down-regulating activity in the c-Met/ERK pathway. PMID: 30108016
++ 30 more research findings link this target to additional biology. Showing the 20 most recent — the full set appears on the complete datasheet.
Involvement in disease
Deafness, autosomal recessive, 39 (DFNB39)
Protein Families
Peptidase S1 family, Plasminogen subfamily
Database Links

HGNC: 4893

OMIM: 142409

KEGG: hsa:3082

STRING: 9606.ENSP00000222390

UniGene: Hs.396530

Precision

Intra-assay Precision (Precision within an assay): CV%<8%

Three samples of known concentration were tested twenty times on one plate to assess.

Inter-assay Precision (Precision between assays): CV%<10%

Three samples of known concentration were tested in twenty assays to assess.

Typical Data

These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed.

Human hepatocyte growth factor,HGF ELISA kit

pg/ml

OD1

OD2

Average

Corrected

1000

1.873

1.953

1.913

1.723

500

1.332

1.307

1.320

1.129

250

0.839

0.903

0.871

0.680

125

0.629

0.619

0.624

0.434

62.5

0.429

0.421

0.425

0.235

31.2

0.323

0.335

0.329

0.139

15.6

0.259

0.248

0.254

0.063

0

0.189

0.193

0.191

Linearity

To assess the linearity of the assay, samples were spiked with high concentrations of human HGF in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay.

Sample

Serum(n=4)

1:1

Average %

89

Range %

80-98

1:2

Average %

90

Range %

85-100

1:4

Average %

95

Range %

92-100

1:8

Average %

93

Range %

86-98

Recovery

The recovery of human HGF spiked to levels throughout the range of the assay in various matrices was evaluated. Samples were diluted prior to assay as directed in the Sample Preparation section.

Sample Type

Average % Recovery

Range

Serum (n=5)

96

91-108

EDTA plasma (n=4)

99

94-105

Peer-reviewed citations
Academic Editor: Carla Perego

A Ummerkutty, C Pace-Asciak  ·  Biomolecules  ·  2025

++ 6 more peer-reviewed citations feature this kit. Showing the 1 most recent — browse every publication on the full product page.

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