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AB117600

Anti-ALIX antibody [3A9]

4

(3 Reviews)

|

(140 Publications)

Anti-ALIX antibody [3A9] (ab117600) is a mouse monoclonal antibody detecting ALIX in Western Blot. Suitable for Human.

- Over 100 publications

View Alternative Names

AIP1, ALIX, KIAA1375, PDCD6IP, Programmed cell death 6-interacting protein, PDCD6-interacting protein, ALG-2-interacting protein 1, ALG-2-interacting protein X, Hp95

1 Images
Western blot - Anti-ALIX antibody [3A9] (AB117600)
  • WB

Unknown

Western blot - Anti-ALIX antibody [3A9] (AB117600)

All lanes:

Western blot - Anti-ALIX antibody [3A9] (ab117600)

All lanes:

HeLa whole cell lysate

Secondary

All lanes:

Rabbit Anti Mouse IgG

Predicted band size: 96 kDa

false

Key facts

Host species

Mouse

Clonality

Monoclonal

Clone number

3A9

Isotype

IgG1

Carrier free

No

Reacts with

Human

Applications

WB

applications

Immunogen

Recombinant Protein within Human PDCD6IP aa 600-750. The exact immunogen used to generate this antibody is proprietary information.

Q8WUM4

Reactivity data

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Product details

What is this antibody validated in?
Anti-ALIX antibody [3A9] (ab117600) is a mouse monoclonal antibody and is validated for use in Western Blot (WB) in Human samples.

What is the molecular weight of ALIX?
Anti-ALIX [3A9] (ab117600) specifically detects a band for ALIX (UniProt: Q8WUM4) at a molecular weight of 96kDa.

Trusted by the scientific community
Anti-ALIX [3A9] (ab117600) was first used in a scientific publication in 2011 and has been cited over 100 times in peer-reviewed journals.

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Protein G
Storage buffer
Preservative: 0.09% Sodium azide Constituents: PBS
Shipped at conditions
Blue Ice
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

Supplementary information

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

ALIX also known as PDCD6IP or ALIX G is an adapter protein involved in various cellular processes. It holds a molecular weight of approximately 95-100 kDa and is widely expressed in different tissue types including HEK 293 cells. ALIX plays a significant role as a component of the endosomal sorting complexes required for transport (ESCRT) machinery contributing to membrane dynamics and intracellular trafficking.
Biological function summary

ALIX acts as an important mediator in the regulation of cellular membrane remodeling. It associates with several protein complexes influencing the budding and fission of vesicles and endosomes. The protein also interacts with ubiquitin and other factors guiding protein sorting and maintaining cellular homeostasis. This adapter characteristic makes ALIX essential for recycling receptors and maintaining cell surface receptor expression levels.

Pathways

ALIX is involved in the ESCRT pathway and the apoptotic pathways. It works closely with proteins like TSG101 and CHMP4 to facilitate vesicle formation and dispatch impacting cellular processes like signaling and waste disposal. Furthermore ALIX regulates apoptosis by interacting with proteins such as ALG-2 and to some extent with apoptosis-related membranes to mediate programmed cell death.

ALIX has established links to cancer progression and neurodegenerative disorders. Its participation in membrane remodeling and protein sorting correlates with tumor development with evidence showing that altered expression affects oncogenic pathways. Additionally dysregulation of ALIX-associated pathways has implications in neurodegenerative diseases where ALIX and proteins such as those in the ESCRT complex could play a role in the degradation of misfolded proteins and endocytic dysfunctions contributing to disease pathology.

Product protocols

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

Target data

Multifunctional protein involved in endocytosis, multivesicular body biogenesis, membrane repair, cytokinesis, apoptosis and maintenance of tight junction integrity. Class E VPS protein involved in concentration and sorting of cargo proteins of the multivesicular body (MVB) for incorporation into intralumenal vesicles (ILVs) that are generated by invagination and scission from the limiting membrane of the endosome. Binds to the phospholipid lysobisphosphatidic acid (LBPA) which is abundant in MVBs internal membranes. The MVB pathway requires the sequential function of ESCRT-O, -I,-II and -III complexes (PubMed : 14739459). The ESCRT machinery also functions in topologically equivalent membrane fission events, such as the terminal stages of cytokinesis (PubMed : 17556548, PubMed : 17853893). Adapter for a subset of ESCRT-III proteins, such as CHMP4, to function at distinct membranes. Required for completion of cytokinesis (PubMed : 17556548, PubMed : 17853893, PubMed : 18641129). May play a role in the regulation of both apoptosis and cell proliferation. Regulates exosome biogenesis in concert with SDC1/4 and SDCBP (PubMed : 22660413). By interacting with F-actin, PARD3 and TJP1 secures the proper assembly and positioning of actomyosin-tight junction complex at the apical sides of adjacent epithelial cells that defines a spatial membrane domain essential for the maintenance of epithelial cell polarity and barrier (By similarity).. (Microbial infection) Involved in HIV-1 virus budding. Can replace TSG101 it its role of supporting HIV-1 release; this function requires the interaction with CHMP4B. The ESCRT machinery also functions in topologically equivalent membrane fission events, such as enveloped virus budding (HIV-1 and other lentiviruses).
See full target information PDCD6IP

Publications (140)

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

Stem cell research & therapy 16:450 PubMed40846969

2025

Inflammatory cytokine-primed MSC-derived extracellular vesicles ameliorate acute lung injury via enhanced immunomodulation and alveolar repair.

Applications

Unspecified application

Species

Unspecified reactive species

Jongwon Jeong,Jun-Kook Park,Jiwon Shin,Inseong Jung,Hyun-Woo Kim,Anyeseu Park,Hanchae Cho,Sung-Min Kang,Sanghee Shin,Eunju Park,Jisuk Kim,Soojeong Noh,Yongdeok Ahn,Do-Kyun Kim,Jeong Yoon Lee,Daeha Seo,Moon-Chang Baek,Kyungmoo Yea

Journal of extracellular biology 4:e70080 PubMed40843441

2025

Surface-Engineered Natural Killer Cell-Derived Small Extracellular Vesicles Induce Potent Anti-Tumour Effects in Lung Cancer Cells.

Applications

Unspecified application

Species

Unspecified reactive species

Sung-Min Kang,Dokyung Jung,Soojeong Noh,Sanghee Shin,Minju Kim,Hanchae Cho,Byungheon Lee,Kyungmoo Yea,Moon-Chang Baek

Journal of nanobiotechnology 23:572 PubMed40830888

2025

hUMSC-Exosomes suppress TREM1-p38 MAPK signaling via HMGB1-dependent mechanisms to reprogram microglial function and promote neuroprotection in ischemic stroke.

Applications

Unspecified application

Species

Unspecified reactive species

Zengyu Zhang,Rong Ji,Zhuohang Liu,Zhiwen Jiang,Min Chu,Yong Wang,Jing Zhao

Journal of extracellular vesicles 14:e70114 PubMed40673783

2025

ADAM Sheddase Activity Promotes the Detachment of Small Extracellular Vesicles From the Plasma Membrane.

Applications

Unspecified application

Species

Unspecified reactive species

Chloé Bizingre,Zaira Arellano-Anaya,Flavien Picard,Mathéa Pietri,Anne Baudry,Florence Roussel,Clara Bianchi,Aurélie Alleaume-Butaux,Hector Ardila-Osorio,Maryse Romao,Grégory Lavieu,Graça Raposo,Benoit Schneider

Advanced science (Weinheim, Baden-Wurttemberg, Germany) 12:e2500599 PubMed40349160

2025

3D-Printed Titanium Trabecular Scaffolds with Sustained Release of Hypoxia-Induced Exosomes for Dual-Mimetic Bone Regeneration.

Applications

Unspecified application

Species

Unspecified reactive species

Lincong Luo,Weihan Zheng,Jiaying Li,Tingting Chen,Wanting Xue,Tao Lin,Mingrui Liu,Zi Yan,Jiaxin Yang,Jiamin Li,Jiahao Pu,Yaobin Wu,Konghe Hu,Shiyu Li,Wenhua Huang

Journal of nanobiotechnology 23:256 PubMed40156015

2025

Autologous platelet delivery of siRNAs by autologous plasma protein self-assembled nanoparticles for the treatment of acute kidney injury.

Applications

Unspecified application

Species

Unspecified reactive species

Jiafan Wang,Hai Huang,Meng Jia,Si Chen,Fengjuan Wang,Guiyang He,Chong Wu,Kaibin Lou,Xuexue Zheng,Heng Zhang,Chao Qin,Yanggang Yuan,Ke Zen,Hongwei Liang

Cell biology and toxicology 41:50 PubMed39992453

2025

Therapeutic role of hucMSC-sEV-enriched miR-13896 in cisplatin-induced acute kidney injury through M2 macrophage polarization.

Applications

Unspecified application

Species

Unspecified reactive species

Can Jin,Peipei Wu,Wei Wu,Wenya Chen,Wanzhu Liu,Yuan Zhu,QiShun Wu,Binghai Chen,Cheng Ji,Hui Qian

Regenerative therapy 28:253-261 PubMed39834593

2025

Systemic administration of induced pluripotent stem cell-derived mesenchymal stem cells improves cardiac function through extracellular vesicle-mediated tissue repair in a rat model of ischemic cardiomyopathy.

Applications

Unspecified application

Species

Unspecified reactive species

Ryo Kawasumi,Takuji Kawamura,Kizuku Yamashita,Yuji Tominaga,Akima Harada,Emiko Ito,Maki Takeda,Shunbun Kita,Iichiro Shimomura,Shigeru Miyagawa

Journal of extracellular vesicles 13:e12523 PubMed39400515

2024

Snorkel-tag based affinity chromatography for recombinant extracellular vesicle purification.

Applications

Unspecified application

Species

Unspecified reactive species

Madhusudhan Reddy Bobbili,André Görgens,Yan Yan,Stefan Vogt,Dhanu Gupta,Giulia Corso,Samir Barbaria,Carolina Patrioli,Sylvia Weilner,Marianne Pultar,Jaroslaw Jacak,Matthias Hackl,Markus Schosserer,Regina Grillari,Jørgen Kjems,Samir El Andaloussi,Johannes Grillari

Cell communication and signaling : CCS 22:452 PubMed39327567

2024

Non-thermal atmospheric pressure plasma induces selective cancer cell apoptosis by modulating redox homeostasis.

Applications

Unspecified application

Species

Unspecified reactive species

Ju Hyun Yun,Yoon Hee Yang,Chang Hak Han,Sung Un Kang,Chul-Ho Kim
View all publications

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