Human IgG antibody Laboratories manufactures the liver fibrosis assay reagents distributed by Genprice. The Liver Fibrosis Assay reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact liver assay. Other Liver products are available in stock. Specificity: Liver Category: Fibrosis Group: Assay
True Blue |
TargetMol Chemicals |
1mg |
Ask for price |
- SMILES: N=C(C1=CC=C(OC(/C=C/C2=CC3=CC(C(N)=N)=CC=C3O2)=C4)C4=C1)N.Cl.Cl
- Formula: C20H18Cl2N4O2
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Description: True Blue |
True Blue |
TargetMol Chemicals |
50mg |
Ask for price |
- SMILES: N=C(C1=CC=C(OC(/C=C/C2=CC3=CC(C(N)=N)=CC=C3O2)=C4)C4=C1)N.Cl.Cl
- Formula: C20H18Cl2N4O2
|
Description: True Blue |
True Blue |
TargetMol Chemicals |
5mg |
Ask for price |
- SMILES: N=C(C1=CC=C(OC(/C=C/C2=CC3=CC(C(N)=N)=CC=C3O2)=C4)C4=C1)N.Cl.Cl
- Formula: C20H18Cl2N4O2
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Description: True Blue |
True Blue |
MedKoo Biosciences |
5.0mg |
EUR 595 |
- Smiles Code: N=C(N)C1=CC=C2C(C=C(/C=C/C3=CC4=C(C=CC(C(N)=N)=C4)O3)O2)=C1.Cl.Cl
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COVID-19 Spike RBD and Membrane Protein Human IgG ELISA Assay |
MyBiosource |
48AntigenWells&48ControlAntigenWells |
EUR 635 |
Assay information
Anti-hepatic fibrosis agent 2 |
HY-154979 |
MedChemExpress |
Get quote |
Ask for price |
Description: Anti-hepatic fibrosis agent 2 (Compound 6k) is an orally active COL1A1 inhibitor. Anti-hepatic fibrosis agent 2 is an anti-fibrogenic agent targeting ewing sarcoma breakpoint region 1 (EWSR1)[1]. |
Pulmonary interstitial fibrosis tissue array |
LC561 |
TissueArray |
each |
EUR 270 |
Description: Pulmonary interstitial fibrosis tissue array, 28 cases/56 cores |
Single Donor Human Pulmonary Fibrosis Serum |
MBS8421623-INQUIRE |
MyBiosource |
INQUIRE |
Ask for price |
Single Donor Human Pulmonary Fibrosis Serum |
ISERSPF |
Innovative research |
each |
EUR 209 |
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Description: Single Donor Human Pulmonary Fibrosis Serum |
Single Donor Human Pulmonary Fibrosis Plasma |
MBS8421079-INQUIRE |
MyBiosource |
INQUIRE |
Ask for price |
Single Donor Human Pulmonary Fibrosis Plasma |
IPLASPF |
Innovative research |
each |
EUR 209 |
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Description: Single Donor Human Pulmonary Fibrosis Plasma |
CFTR Antibody / Cystic Fibrosis Transmembrane Regulator |
V3672-100UG |
NSJ Bioreagents |
100 ug |
EUR 349.3 |
- 0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced) and 0.05% sodium azide
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Description: Cystic fibrosis transmembrane conductance regulator (CFTR) is a membrane protein and chloride channel in vertebrates that is encoded by the CFTR gene. The CFTR gene codes for an ABC transporter-class ion channel protein that conducts chloride and thiocyanate ions across epithelial cell membranes. Mutations of the CFTR gene affecting chloride ion channel function lead to dysregulation of epithelial fluid transport in the lung, pancreas and other organs, resulting in cystic fibrosis. Complications include thickened mucus in the lungs with frequent respiratory infections, and pancreatic insufficiency giving rise to malnutrition and diabetes. These conditions lead to chronic disability and reduced life expectancy. In male patients, the progressive obstruction and destruction of the developing vas deferens (spermatic cord) and epididymis appear to result from abnormal intraluminal secretions, causing congenital absence of the vas deferens and male infertility. [Wiki] |
CFTR Antibody / Cystic Fibrosis Transmembrane Regulator |
V3672-20UG |
NSJ Bioreagents |
20 ug |
EUR 153.3 |
- 0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced) and 0.05% sodium azide
|
Description: Cystic fibrosis transmembrane conductance regulator (CFTR) is a membrane protein and chloride channel in vertebrates that is encoded by the CFTR gene. The CFTR gene codes for an ABC transporter-class ion channel protein that conducts chloride and thiocyanate ions across epithelial cell membranes. Mutations of the CFTR gene affecting chloride ion channel function lead to dysregulation of epithelial fluid transport in the lung, pancreas and other organs, resulting in cystic fibrosis. Complications include thickened mucus in the lungs with frequent respiratory infections, and pancreatic insufficiency giving rise to malnutrition and diabetes. These conditions lead to chronic disability and reduced life expectancy. In male patients, the progressive obstruction and destruction of the developing vas deferens (spermatic cord) and epididymis appear to result from abnormal intraluminal secretions, causing congenital absence of the vas deferens and male infertility. [Wiki] |
CFTR Antibody / Cystic Fibrosis Transmembrane Regulator |
V3672IHC-7ML |
NSJ Bioreagents |
7 ml |
EUR 349.3 |
- Prediluted in 1X PBS with 0.1 mg/ml BSA (US sourced) and 0.05% sodium azide
- *For IHC use only*
|
Description: Cystic fibrosis transmembrane conductance regulator (CFTR) is a membrane protein and chloride channel in vertebrates that is encoded by the CFTR gene. The CFTR gene codes for an ABC transporter-class ion channel protein that conducts chloride and thiocyanate ions across epithelial cell membranes. Mutations of the CFTR gene affecting chloride ion channel function lead to dysregulation of epithelial fluid transport in the lung, pancreas and other organs, resulting in cystic fibrosis. Complications include thickened mucus in the lungs with frequent respiratory infections, and pancreatic insufficiency giving rise to malnutrition and diabetes. These conditions lead to chronic disability and reduced life expectancy. In male patients, the progressive obstruction and destruction of the developing vas deferens (spermatic cord) and epididymis appear to result from abnormal intraluminal secretions, causing congenital absence of the vas deferens and male infertility. [Wiki] |
CFTR Antibody / Cystic Fibrosis Transmembrane Regulator |
V3672SAF-100UG |
NSJ Bioreagents |
100 ug |
EUR 349.3 |
- 1 mg/ml in 1X PBS
- BSA free, sodium azide free
|
Description: Cystic fibrosis transmembrane conductance regulator (CFTR) is a membrane protein and chloride channel in vertebrates that is encoded by the CFTR gene. The CFTR gene codes for an ABC transporter-class ion channel protein that conducts chloride and thiocyanate ions across epithelial cell membranes. Mutations of the CFTR gene affecting chloride ion channel function lead to dysregulation of epithelial fluid transport in the lung, pancreas and other organs, resulting in cystic fibrosis. Complications include thickened mucus in the lungs with frequent respiratory infections, and pancreatic insufficiency giving rise to malnutrition and diabetes. These conditions lead to chronic disability and reduced life expectancy. In male patients, the progressive obstruction and destruction of the developing vas deferens (spermatic cord) and epididymis appear to result from abnormal intraluminal secretions, causing congenital absence of the vas deferens and male infertility. [Wiki] |
CFTR Antibody / Cystic Fibrosis Transmembrane Regulator |
V9326-100UG |
NSJ Bioreagents |
100ug |
EUR 349.3 |
- 0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced), 0.05% sodium azide
|
Description: Recognizes a protein of 165-170kDa, identified as cystic fibrosis transmembrane conductance regulator (CFTR). CFTR is composed of two membrane-spanning domains (MSD), two nucleotide-binding domains (NBD), and an R domain. It is structurally similar to multidrug resistance (Mdr1) protein and both are members of the superfamily of ATP-binding cassette (ABC) transporters, also known as traffic ATPases, which are implicated in the movement of various substrates. The CFTR protein is a small conductance adenosine 3-cyclic monophosphate (cAMP)-activated chloride ion channel found in the apical membranes of epithelia within the pancreas, airway, intestine, bile duct, sweat gland, and male genital ducts. CFTR is a valuable marker of human pancreatic duct cell development and differentiation. |
CFTR Antibody / Cystic Fibrosis Transmembrane Regulator |
V9326-20UG |
NSJ Bioreagents |
20ug |
EUR 153.3 |
- 0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced), 0.05% sodium azide
|
Description: Recognizes a protein of 165-170kDa, identified as cystic fibrosis transmembrane conductance regulator (CFTR). CFTR is composed of two membrane-spanning domains (MSD), two nucleotide-binding domains (NBD), and an R domain. It is structurally similar to multidrug resistance (Mdr1) protein and both are members of the superfamily of ATP-binding cassette (ABC) transporters, also known as traffic ATPases, which are implicated in the movement of various substrates. The CFTR protein is a small conductance adenosine 3-cyclic monophosphate (cAMP)-activated chloride ion channel found in the apical membranes of epithelia within the pancreas, airway, intestine, bile duct, sweat gland, and male genital ducts. CFTR is a valuable marker of human pancreatic duct cell development and differentiation. |
CFTR Antibody / Cystic Fibrosis Transmembrane Regulator |
V9326SAF-100UG |
NSJ Bioreagents |
100ug |
EUR 349.3 |
- 1 mg/ml in 1X PBS
- BSA free, sodium azide free
|
Description: Recognizes a protein of 165-170kDa, identified as cystic fibrosis transmembrane conductance regulator (CFTR). CFTR is composed of two membrane-spanning domains (MSD), two nucleotide-binding domains (NBD), and an R domain. It is structurally similar to multidrug resistance (Mdr1) protein and both are members of the superfamily of ATP-binding cassette (ABC) transporters, also known as traffic ATPases, which are implicated in the movement of various substrates. The CFTR protein is a small conductance adenosine 3-cyclic monophosphate (cAMP)-activated chloride ion channel found in the apical membranes of epithelia within the pancreas, airway, intestine, bile duct, sweat gland, and male genital ducts. CFTR is a valuable marker of human pancreatic duct cell development and differentiation. |
CFTR Antibody / Cystic Fibrosis Transmembrane Regulator |
V9336-100UG |
NSJ Bioreagents |
100ug |
EUR 349.3 |
- 0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced), 0.05% sodium azide
|
Description: Recognizes a protein of 165-170kDa, identified as cystic fibrosis transmembrane conductance regulator (CFTR). CFTR is composed of two membrane-spanning domains (MSD), two nucleotide-binding domains (NBD), and an R domain. It is structurally similar to multidrug resistance (Mdr1) protein and both are members of the superfamily of ATP-binding cassette (ABC) transporters, also known as traffic ATPases, which are implicated in the movement of various substrates. The CFTR protein is a small conductance adenosine 3-cyclic monophosphate (cAMP)-activated chloride ion channel found in the apical membranes of epithelia within the pancreas, airway, intestine, bile duct, sweat gland, and male genital ducts. CFTR is a valuable marker of human pancreatic duct cell development and differentiation. |
CFTR Antibody / Cystic Fibrosis Transmembrane Regulator |
V9336-20UG |
NSJ Bioreagents |
20ug |
EUR 153.3 |
- 0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced), 0.05% sodium azide
|
Description: Recognizes a protein of 165-170kDa, identified as cystic fibrosis transmembrane conductance regulator (CFTR). CFTR is composed of two membrane-spanning domains (MSD), two nucleotide-binding domains (NBD), and an R domain. It is structurally similar to multidrug resistance (Mdr1) protein and both are members of the superfamily of ATP-binding cassette (ABC) transporters, also known as traffic ATPases, which are implicated in the movement of various substrates. The CFTR protein is a small conductance adenosine 3-cyclic monophosphate (cAMP)-activated chloride ion channel found in the apical membranes of epithelia within the pancreas, airway, intestine, bile duct, sweat gland, and male genital ducts. CFTR is a valuable marker of human pancreatic duct cell development and differentiation. |
CFTR Antibody / Cystic Fibrosis Transmembrane Regulator |
V9336SAF-100UG |
NSJ Bioreagents |
100ug |
EUR 349.3 |
- 1 mg/ml in 1X PBS
- BSA free, sodium azide free
|
Description: Recognizes a protein of 165-170kDa, identified as cystic fibrosis transmembrane conductance regulator (CFTR). CFTR is composed of two membrane-spanning domains (MSD), two nucleotide-binding domains (NBD), and an R domain. It is structurally similar to multidrug resistance (Mdr1) protein and both are members of the superfamily of ATP-binding cassette (ABC) transporters, also known as traffic ATPases, which are implicated in the movement of various substrates. The CFTR protein is a small conductance adenosine 3-cyclic monophosphate (cAMP)-activated chloride ion channel found in the apical membranes of epithelia within the pancreas, airway, intestine, bile duct, sweat gland, and male genital ducts. CFTR is a valuable marker of human pancreatic duct cell development and differentiation. |
CFTR Antibody / Cystic Fibrosis Transmembrane Regulator |
V9382-100UG |
NSJ Bioreagents |
100ug |
EUR 349.3 |
- 0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced), 0.05% sodium azide
|
Description: Recognizes a protein of 165-170kDa, identified as cystic fibrosis transmembrane conductance regulator (CFTR). CFTR is composed of two membrane-spanning domains (MSD), two nucleotide-binding domains (NBD), and an R domain. It is structurally similar to multidrug resistance (Mdr1) protein and both are members of the superfamily of ATP-binding cassette (ABC) transporters, also known as traffic ATPases, which are implicated in the movement of various substrates. The CFTR protein is a small conductance adenosine 3-cyclic monophosphate (cAMP)-activated chloride ion channel found in the apical membranes of epithelia within the pancreas, airway, intestine, bile duct, sweat gland, and male genital ducts. CFTR is a valuable marker of human pancreatic duct cell development and differentiation. |