Human HGF Recombinant Rabbit Monoclonal Antibody [PSH02-06] - BSA and Azide free (Capture)
Overview
Product Name
Human HGF Recombinant Rabbit Monoclonal Antibody [PSH02-06] - BSA and Azide free (Capture)
Antibody Type
Recombinant Rabbit monoclonal Antibody
Immunogen
Recombinant protein within Human HGF aa 32-494 (P14210).
Species Reactivity
Human
Validated Applications
ELISA(Cap)
Molecular Weight
Predicted band size: 83 kDa
Positive Control
Recombinant Human HGF protein.
Conjugation
unconjugated
Clone Number
PSH02-06
RRID
Product Features
Form
Liquid
Concentration
Storage Instructions
Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage Buffer
PBS (pH7.4).
Isotype
IgG
Purification Method
Protein A affinity purified.
Application Dilution
-
ELISA(Cap)
-
Use at an assay dependent concentration. Can be paired for Sandwich ELISA with Rabbit monoclonal [PSH02-07] to Human HGF (Detector) (HA721779). The reference range value is 12.35-3,000 pg/mL.
Target
Function
HGF, also known as scatter factor and hepatopoietin A, is a pleiotropic protein in the plasminogen subfamily of S1 peptidases. It is a multidomain molecule that includes an N-terminal PAN/APPLE-like domain, four Kringle domains, and a serine proteinase-like domain that has no detectable protease activity Human HGF is secreted as an inactive 728 amino acid (aa) single chain propeptide. It is cleaved after the fourth Kringle domain by a serine protease to form bioactive disulfide-linked HGF with a 60 kDa alpha and 30 kDa beta chain. Alternate splicing generates human HGF isoforms that lack the proteinase-like domain and different numbers of the Kringle domains. Human HGF shares 91%-94% aa sequence identity with bovine, canine, feline, mouse, and rat HGF. HGF binds heparan-sulfate proteoglycans and the widely expressed receptor tyrosine kinase, HGF R/c-MET. HGF-dependent c-MET activation is implicated in the development of many human cancers. HGF regulates epithelial morp.
Background References
1. Zhao Y et al. HGF/c-Met: A Key Promoter in Liver Regeneration. Front Pharmacol. 2022 Mar
2. Pothula SP et al. Targeting HGF/c-MET Axis in Pancreatic Cancer. Int J Mol Sci. 2020 Dec
Subcellular Location
Extracellular region, extracellular space, membrane, platelet alpha granule lumen.
UNIPROT
Synonyms
DFNB39 antibody
F TCF antibody
Fibroblast derived tumor cytotoxic factor antibody
Hepatocyte growth factor (hepapoietin A
scatter factor) antibody
Hepatocyte growth factor antibody
Hepatocyte growth factor beta chain antibody
Hepatocyte growth factor precursor antibody
Hepatopoietin A antibody
Hepatopoietin-A antibody
ExpandImages
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![Sandwich ELISA analysis of human HGF matched pair antibodies.<br /><br />Elisa assay was performed by coating wells of a 96-well plate with 100 µl per well of capture antibody (<a href="/products/HA721778" style="font-weight: bold;text-decoration: underline;">HA721778</a>) diluted in carbonate/bicarbonate buffer, at a concentration of 2 µg/ml overnight at 4℃. Wells of the plate were washed, blocked with 150 µl 0.05% tween-20 1%BSA blocking buffer, and incubated with serial diluted human HGF protein starting from 3000 pg/ml to 0 pg/ml and detect antibody [PSH02-07]-Biotin for 1 hour at 30℃ with shaking. Then the plate was washed and incubated with 100 µl per well of SA-HRP for 0.5 hour at 30℃ with shaking. Detection was performed using an Ultra TMB Substrate for 10 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm.](https://storage.huabio.cn/huabio/productImg/HA721778_1.jpg?v=20260509231353)
Sandwich ELISA analysis of human HGF matched pair antibodies.
Elisa assay was performed by coating wells of a 96-well plate with 100 µl per well of capture antibody (HA721778) diluted in carbonate/bicarbonate buffer, at a concentration of 2 µg/ml overnight at 4℃. Wells of the plate were washed, blocked with 150 µl 0.05% tween-20 1%BSA blocking buffer, and incubated with serial diluted human HGF protein starting from 3000 pg/ml to 0 pg/ml and detect antibody [PSH02-07]-Biotin for 1 hour at 30℃ with shaking. Then the plate was washed and incubated with 100 µl per well of SA-HRP for 0.5 hour at 30℃ with shaking. Detection was performed using an Ultra TMB Substrate for 10 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
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