MABT366
Anti-Claudin-1/CLDN1 Antibody, clone 7A5
clone 7A5, from mouse
Synonym(s):
Claudin-1, Senescence-associated epithelial membrane protein
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About This Item
UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41
Recommended Products
biological source
mouse
Quality Level
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
7A5, monoclonal
species reactivity
human
should not react with
mouse
technique(s)
flow cytometry: suitable
immunocytochemistry: suitable
western blot: suitable
isotype
IgG1κ
NCBI accession no.
UniProt accession no.
shipped in
dry ice
target post-translational modification
unmodified
Gene Information
human ... CLDN1(9076) , NISCH(11188)
Related Categories
General description
Claudin-1 (UniProt O95832; also known as Senescence-associated epithelial membrane protein) is encoded by the CLDN1 (also known as CLD1, ILVASC, NISCH, SEMP1) gene (ORF UNQ481/PRO944; Gene ID 9076) in human. Tight junctions (TJs) are highly specialized membrane barriers that block the free passage of small molecules, microorganisms, and cells across the paracellular space, as well as provide a physical barrier between the apical and basolateral membrane domains of a polarized epithelial cell. Claudins are TJ proteins whose main function is to regulate the passage of ions across the paracellular space. There exist at least 27 human claudins with differential epithelial expression patterns, allowing tissue-specific paracellular transport of ions. Claudin-1 is expressed on apical and basolateral surfaces of hepatocytes in normal liver tissue. Claudin-1 is a known host factor for hepatitis C virus (HCV) entry via interaction with CD81 and cell-to-cell HCV transmission. Claudin-1 is a four-transmembrane (a.a. 8-28, 82-102, 116-136, 164-184) protein, having both its N- and C-terminal ends exposed cytoplasmically (a.a. 1-7 & 185-211).
Specificity
Clone 7A5 specifically recognized human claudin-1/CLDN1 by targeting an epitope in the second extracellular loop and prevented claudin-1-dependent hepatitis C virus (HCV) entry into host cells. Clone 7A5 does not react with human claudin-2, -4, -5, -6, -7, or -9, nor mouse claudin-1 (Fukasawa, M., et al. (2015). J. Virol. 89(9):4866-4879).
Immunogen
Epitope: Second extracellular loop.
Recombinant human Claudin-1/CLDN1.
Application
Flow Cytometry Analysis: 5.0 µg/mL from a representative lot immunostained HT1080 cells expressing exogenously transfected human claudin-1/CLDN1 and Huh-7.5.1 human hepatoma cells, but not mock-transfected HT1080 cells or non-claudin-1-expressing S7-d6 cells (Courtesy of Professor Masuo Kondoh, PhD, Osaka University, Japan).
Western Blotting Analysis: 0.5 µg/mL from a representative lot detected exogenously expressed claudin-1 in CLDN1-transfected, but not mock-transfected, HT1080 cells (Courtesy of Professor Masuo Kondoh, PhD, Osaka University, Japan).
Immunocytochemistry Analysis: A representative lot immunostained the surface of Huh-7.5.1 human hepatoma cells, but not the non-claudin-1-/CLDN1-expressing S7-A cells (Fukasawa, M., et al. (2015). J. Virol. 89(9):4866-4879).
Flow Cytometry Analysis: A representative lot specifically immunostained HT1080 cells expressing exogenously transfected human claudin-1 (CLDN1), but not HT1080 cells expressing human claudin-2, -4, -5, -6, -7, or -9, nor L cells expressing mouse claudin-1 (Fukasawa, M., et al. (2015). J. Virol. 89(9):4866-4879).
Flow Cytometry Analysis: A representative lot immunostained HEK293T transfectants expressing FLAG-tagged human claudin-1/CLDN1 and human-mouse claudin-1 chimeras with the second human extracellular loop (EL2), but not chimeras with the mouse EL2. M152L, but not V155I, mutation in human EL2 abolished the immunoreactivity (Fukasawa, M., et al. (2015). J. Virol. 89(9):4866-4879).
Western Blotting Analysis: A representative lot detected FLAG-tagged human claudin-1/CLDN1 and human-mouse claudin-1 chimeras with the second human extracellular loop (EL2), but not chimeras with the mouse EL2. M152L, but not V155I, mutation in the second human extracellular loop abolished the immunoreactivity (Fukasawa, M., et al. (2015). J. Virol. 89(9):4866-4879).
ELISA Analysis: A representative lot detected claudin-1/CLDN1 immunoreactivity in 3.7% formaldehyde-fixed Huh-7.5.1 human hepatoma cells by "cell ELISA" (Fukasawa, M., et al. (2015). J. Virol. 89(9):4866-4879).
Neutralization Analysis: A representative lot inhibited HCV infection of cultured Huh-7.5.1 human hepatoma cells in vitro and of human liver-chimeric mice in vivo (Fukasawa, M., et al. (2015). J. Virol. 89(9):4866-4879).
Western Blotting Analysis: 0.5 µg/mL from a representative lot detected exogenously expressed claudin-1 in CLDN1-transfected, but not mock-transfected, HT1080 cells (Courtesy of Professor Masuo Kondoh, PhD, Osaka University, Japan).
Immunocytochemistry Analysis: A representative lot immunostained the surface of Huh-7.5.1 human hepatoma cells, but not the non-claudin-1-/CLDN1-expressing S7-A cells (Fukasawa, M., et al. (2015). J. Virol. 89(9):4866-4879).
Flow Cytometry Analysis: A representative lot specifically immunostained HT1080 cells expressing exogenously transfected human claudin-1 (CLDN1), but not HT1080 cells expressing human claudin-2, -4, -5, -6, -7, or -9, nor L cells expressing mouse claudin-1 (Fukasawa, M., et al. (2015). J. Virol. 89(9):4866-4879).
Flow Cytometry Analysis: A representative lot immunostained HEK293T transfectants expressing FLAG-tagged human claudin-1/CLDN1 and human-mouse claudin-1 chimeras with the second human extracellular loop (EL2), but not chimeras with the mouse EL2. M152L, but not V155I, mutation in human EL2 abolished the immunoreactivity (Fukasawa, M., et al. (2015). J. Virol. 89(9):4866-4879).
Western Blotting Analysis: A representative lot detected FLAG-tagged human claudin-1/CLDN1 and human-mouse claudin-1 chimeras with the second human extracellular loop (EL2), but not chimeras with the mouse EL2. M152L, but not V155I, mutation in the second human extracellular loop abolished the immunoreactivity (Fukasawa, M., et al. (2015). J. Virol. 89(9):4866-4879).
ELISA Analysis: A representative lot detected claudin-1/CLDN1 immunoreactivity in 3.7% formaldehyde-fixed Huh-7.5.1 human hepatoma cells by "cell ELISA" (Fukasawa, M., et al. (2015). J. Virol. 89(9):4866-4879).
Neutralization Analysis: A representative lot inhibited HCV infection of cultured Huh-7.5.1 human hepatoma cells in vitro and of human liver-chimeric mice in vivo (Fukasawa, M., et al. (2015). J. Virol. 89(9):4866-4879).
Research Category
Cell Structure
Cell Structure
Research Sub Category
Infectious Diseases - Viral
Infectious Diseases - Viral
This Anti-Claudin-1 Antibody, clone 7A5 is validated for use in Immunocytochemistry, Western Blotting, Flow Cytometry for the detection of CLDN1.
Quality
Evaluated by Immunocytochemistry in HepG2 cells.
Immunocytochemistry Analysis: 10 µg/mL of this antibody detected Claudin-1/CLDN1 in HepG2 cells.
Immunocytochemistry Analysis: 10 µg/mL of this antibody detected Claudin-1/CLDN1 in HepG2 cells.
Target description
~20 kDa observed. 22.74 kDa calculated.
Physical form
Format: Purified
Protein G purified.
Purified mouse monoclonal IgG1κ antibody in PBS without preservatives.
Storage and Stability
Stable for 1 year at -20°C from date of receipt.
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
Other Notes
Concentration: Please refer to lot specific datasheet.
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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Description
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Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Hiroki Sakamoto et al.
Scientific reports, 14(1), 3312-3312 (2024-02-09)
Tight junctions (TJs) are important factors constituting the physical barriers of the skin, and their suppression has been described in various conditions, such as aged skin and atopic dermatitis lesions. However, the methods for improving skin TJ function remain insufficient.
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