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AB239238

Biotin Anti-CD81 antibody [M38]

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(5 Publications)

Anti-CD81 antibody [M38] - Biotin conjugated (ab239238) is a mouse monoclonal antibody detecting CD81 in Flow Cytometry. Suitable for Human.

View Alternative Names

CD81, TAPA1, TSPAN28, CD81 antigen, 26 kDa cell surface protein TAPA-1, Target of the antiproliferative antibody 1, Tetraspanin-28, Tspan-28

1 Images
Flow Cytometry - Biotin Anti-CD81 antibody [M38] (AB239238)
  • Flow Cyt

Supplier Data

Flow Cytometry - Biotin Anti-CD81 antibody [M38] (AB239238)

Surface staining of CD81 in human peripheral blood with ab239238, streptavidin-APC.

Key facts

Host species

Mouse

Clonality

Monoclonal

Clone number

M38

Isotype

IgG1

Conjugation

Biotin

Excitation/Emission
Carrier free

No

Reacts with

Human

Applications

Flow Cyt

applications

Immunogen

Cell preparation containing CD81 protein. The exact immunogen used to generate this antibody is proprietary information.

P60033

Reactivity data

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Product details

What is this antibody validated in?
Biotin Anti-CD81 antibody [M38] (ab239238) is a mouse monoclonal antibody and is validated for use in Flow Cytometry (Flow Cyt) in Human samples.

Related products
Antibody clone M38 is also available pre-conjugated to a variety of labels for your convenience – Anti-CD81 Biotin [M38] (ab239238).

Other related products
We have a range of other formats of antibody clone [M38] also available for your convenience: ab79559, ab200565, APC - ab233259, Biotin - ab239238, FITC - ab239256

Properties and storage information

Form
Liquid
Purification technique
Size-exclusion chromatography
Purification notes
The purified antibody is conjugated with Biotin-LC-NHS under optimum conditions.The reagent is free of unconjugated biotin.
Storage buffer
pH: 7.4 Preservative: 0.0975% Sodium azide Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle|Store in the dark

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

CD81 also known as TAPA-1 or 26 kDa protein is a member of the tetraspanin family featuring four transmembrane domains. The molecular weight of CD81 is approximately 26-28 kDa. This protein exhibits expression in numerous cell types such as leukocytes endothelial cells and epithelial tissues. CD81 plays a mechanical role by facilitating membrane protein interactions and contributing to cellular processes like adhesion and morphogenesis. Researchers have identified specific isoforms like M38 and labels like 1D6 CHAN in studies involving this target often analyzing CD81 through techniques like Western blot to determine expression levels and molecular weight.
Biological function summary

CD81 interacts with other tetraspanins and forms complexes within the membrane to regulate cellular signaling trafficking and adhesion. It participates in the assembly of larger tetraspanin-enriched microdomains which are important for efficient signaling and functional variety. These complexes modulate cell morphology proliferation and development influencing immune responses and pathogen entry to cells. The presence of CD81 in diverse tissues implies its involvement in a wide range of cellular processes forming essential complexes with proteins like integrins that further engage in tissue repair and immunological defense.

Pathways

CD81 plays significant roles in the immune system and viral entry pathways. It interacts with other proteins like CD9 and CD19 within the immune response pathways regulating lymphocyte activation and differentiation. CD81 is notably a coreceptor in the hepatitis C virus (HCV) entry pathway facilitating viral attachment and fusion into host cells. These interactions illustrate CD81's involvement in modulation of immune cell responses and influence on pathogen infection processes integrating into the complex cellular pathways important for maintaining homeostasis and response to external stimuli.

CD81 has connections to hepatitis C virus (HCV) infections and immunological disorders such as systemic lupus erythematosus (SLE). During HCV infection CD81 serves as an important entry point for the virus interacting with proteins like claudin-1 and scavenger receptor class B type I (SR-BI) enabling viral entry and replication within liver cells. In SLE alterations in CD81 expression can impact autoantibody production and lymphocyte behavior contributing to the disease's pathology. Understanding CD81's role in these diseases provides insight into therapeutic targets and potential interventions for managing infections and autoimmune responses.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Structural component of specialized membrane microdomains known as tetraspanin-enriched microdomains (TERMs), which act as platforms for receptor clustering and signaling. Essential for trafficking and compartmentalization of CD19 receptor on the surface of activated B cells (PubMed : 16449649, PubMed : 20237408, PubMed : 27881302). Upon initial encounter with microbial pathogens, enables the assembly of CD19-CR2/CD21 and B cell receptor (BCR) complexes at signaling TERMs, lowering the threshold dose of antigen required to trigger B cell clonal expansion and antibody production (PubMed : 15161911, PubMed : 20237408). In T cells, facilitates the localization of CD247/CD3 zeta at antigen-induced synapses with B cells, providing for costimulation and polarization toward T helper type 2 phenotype (PubMed : 22307619, PubMed : 23858057, PubMed : 8766544). Present in MHC class II compartments, may also play a role in antigen presentation (PubMed : 8409388, PubMed : 8766544). Can act both as positive and negative regulator of homotypic or heterotypic cell-cell fusion processes. Positively regulates sperm-egg fusion and may be involved in acrosome reaction (By similarity). In myoblasts, associates with CD9 and PTGFRN and inhibits myotube fusion during muscle regeneration (By similarity). In macrophages, associates with CD9 and beta-1 and beta-2 integrins, and prevents macrophage fusion into multinucleated giant cells specialized in ingesting complement-opsonized large particles (PubMed : 12796480). Also prevents the fusion of mononuclear cell progenitors into osteoclasts in charge of bone resorption (By similarity). May regulate the compartmentalization of enzymatic activities. In T cells, defines the subcellular localization of dNTPase SAMHD1 and permits its degradation by the proteasome, thereby controlling intracellular dNTP levels (PubMed : 28871089). Also involved in cell adhesion and motility. Positively regulates integrin-mediated adhesion of macrophages, particularly relevant for the inflammatory response in the lung (By similarity).. (Microbial infection) Acts as a receptor for hepatitis C virus (HCV) in hepatocytes. Association with CLDN1 and the CLDN1-CD81 receptor complex is essential for HCV entry into host cell.. (Microbial infection) Involved in SAMHD1-dependent restriction of HIV-1 replication. May support early replication of both R5- and X4-tropic HIV-1 viruses in T cells, likely via proteasome-dependent degradation of SAMHD1.. (Microbial infection) Specifically required for Plasmodium falciparum infectivity of hepatocytes, controlling sporozoite entry into hepatocytes via the parasitophorous vacuole and subsequent parasite differentiation to exoerythrocytic forms.
See full target information CD81

Publications (5)

Recent publications for all applications. Explore the full list and refine your search

The Tohoku journal of experimental medicine : PubMed40571642

2025

Modulation of Th17/Treg Balance by Total Flavonoids from Semen Cuscutae through PGRMC2 in a Diminished Ovarian Reserve Rat Model.

Applications

Unspecified application

Species

Unspecified reactive species

Ting Zhou,Shanshan Xu,Juan Tang,Xiaomei Han,Yu Jiang,Huaying Chen

Advanced science (Weinheim, Baden-Wurttemberg, Germany) 12:e2416711 PubMed40285610

2025

Extracellular Vesicular Delta-Like Ligand 3 and Subtype Transcription Factors for Small Cell Lung Cancer Diagnosis.

Applications

Unspecified application

Species

Unspecified reactive species

Hong Li,Chi-Ling Chiang,Kwang Joo Kwak,Hsin-Lun Lee,Xinyu Wang,Giulia Romano,Michela Saviana,Robin Toft,Tai-Shan Cheng,Yuehshih Chang,Bi-Da Hsiang,Guan-Wan Liu,Xiaokui Mo,Yifan Ma,Junjie Pan,Xilal Y Rima,Truc Nguyen Kim,Eduardo Reategui,Chia-Ning Shen,Yeh-Shiu Chu,Carlo Croce,Peter Mu-Hsin Chang,Yi-Chen Yeh,David P Carbone,Chi-Ying F Huang,Chi-Lu Chiang,Patrick Nana-Sinkam,L James Lee

Cell reports. Medicine 6:101999 PubMed40056910

2025

Single extracellular vesicle detection assay identifies membrane-associated α-synuclein as an early-stage biomarker in Parkinson's disease.

Applications

Unspecified application

Species

Unspecified reactive species

Shijun Yan,Wenjing Zhang,Xinying Li,Suman Dutta,Andrew R Castle,Yiming Liu,Anis Sahoo,Chor Lai Lam,Nicholas J F Gatford,Michele T Hu,Chen-Zhong Li,Cheng Jiang,Bowen Shu,George K Tofaris

iScience 27:109866 PubMed38840839

2024

An electro-optical platform for the ultrasensitive detection of small extracellular vesicle sub-types and their protein epitope counts.

Applications

Unspecified application

Species

Unspecified reactive species

Tomás Dias,Ricardo Figueiras,Susana Vagueiro,Renato Domingues,Yu-Hsien Hung,Jagriti Sethi,Elnaz Persia,Pierre Arsène

Advanced science (Weinheim, Baden-Wurttemberg, Germany) 11:e2306373 PubMed38204202

2024

Extracellular Vesicular Analysis of Glypican 1 mRNA and Protein for Pancreatic Cancer Diagnosis and Prognosis.

Applications

Unspecified application

Species

Unspecified reactive species

Hong Li,Chi-Ling Chiang,Kwang Joo Kwak,Xinyu Wang,Sital Doddi,Lakshmi V Ramanathan,Sun M Cho,Ya-Chin Hou,Tai-Shan Cheng,Xiaokui Mo,Yueh-Shih Chang,Hui-Lan Chang,Weiming Cheng,Wei-Ni Tsai,Luong T H Nguyen,Junjie Pan,Yifan Ma,Xilal Y Rima,Jingjing Zhang,Eduardo Reategui,Yeh-Shiu Chu,Peter Mu-Hsin Chang,Pei-Hung Chang,Chi-Ying F Huang,Cheng-Hsu Wang,Yan-Shen Shan,Chung-Pin Li,Martin Fleisher,L James Lee
View all publications

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