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AB207697

Anti-ARL8B antibody

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(3 Publications)

Rabbit Polyclonal ARL8B antibody. Suitable for WB and reacts with Human samples. Cited in 3 publications. Immunogen corresponding to Recombinant Fragment Protein within Human ARL8B aa 1 to C-terminus.

View Alternative Names

ARL10C, GIE1, ARL8B, ADP-ribosylation factor-like protein 8B, ADP-ribosylation factor-like protein 10C, Novel small G protein indispensable for equal chromosome segregation 1

1 Images
Western blot - Anti-ARL8B antibody (AB207697)
  • WB

Supplier Data

Western blot - Anti-ARL8B antibody (AB207697)

All lanes:

Western blot - Anti-ARL8B antibody (ab207697) at 1/1000 dilution

All lanes:

Jurkat cell lysate

Predicted band size: 21 kDa

Observed band size: 15 kDa

false

Key facts

Host species

Rabbit

Clonality

Polyclonal

Isotype

IgG

Carrier free

No

Reacts with

Human

Applications

WB

applications

Immunogen

Recombinant Fragment Protein within Human ARL8B aa 1 to C-terminus. The exact immunogen used to generate this antibody is proprietary information.

Q9NVJ2

Reactivity data

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Properties and storage information

Form
Lyophilized
Reconstitution
reconstitute with water at 200µL
Purification technique
Affinity purification Immunogen
Storage buffer
pH: 7.2 Preservative: 0.02% Sodium azide Constituents: PBS, 1% BSA
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

Supplementary information

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

ARL8B also known as ADP-ribosylation factor-like protein 8B is a small GTPase with an approximate molecular mass of 22 kDa. It mainly localizes to the lysosomal membrane. This protein plays an important role in the regulation of intracellular trafficking and lysosome positioning. ARL8B is expressed across many tissues suggesting its involvement in broad cellular functions.
Biological function summary

ARL8B helps manage the proper function of lysosomes by facilitating their movement and fusion with other cellular compartments. It forms a complex with other proteins such as PLEKHM2 and HOPS which are necessary for tethering events during lysosomal trafficking. This protein contributes to cellular processes such as autophagy and antigen presentation influencing the cell's ability to maintain homeostasis and effectively respond to external stimuli.

Pathways

ARL8B participates in the autophagy pathway and plays a part in the lysosome-related processes. It works closely with proteins like the kinesin motor proteins which drive the movement of lysosomes along microtubules. Through these interactions ARL8B coordinates with other autophagy-related proteins to ensure efficient degradation of cellular debris and recycling of components which are important for cellular health and function.

ARL8B has links to neurodegenerative diseases and immune system dysfunctions. Dysregulation of lysosomal positioning and movement caused by abnormal ARL8B function can lead to conditions such as Charcot-Marie-Tooth disease and impaired immune responses. Furthermore ARL8B interacts with proteins like Rab7a which can have implications in disease pathways emphasizing its significant role in maintaining cellular balance.

Product protocols

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

Target data

Small GTPase which cycles between active GTP-bound and inactive GDP-bound states (PubMed : 15331635, PubMed : 16537643). In its active state, binds to a variety of effector proteins playing a key role in the regulation of lysosomal positioning which is important for nutrient sensing, natural killer cell-mediated cytotoxicity and antigen presentation. Along with its effectors, orchestrates lysosomal transport and fusion (PubMed : 16537643, PubMed : 16650381, PubMed : 25898167, PubMed : 27808481, PubMed : 28325809). Localizes specifically to lysosomal membranes and mediates anterograde lysosomal motility by recruiting PLEKHM2, which in turn recruits the motor protein kinesin-1 on lysosomes. Required for lysosomal and cytolytic granule exocytosis (PubMed : 22172677, PubMed : 24088571, PubMed : 29592961). Critical factor involved in NK cell-mediated cytotoxicity. Drives the polarization of cytolytic granules and microtubule-organizing centers (MTOCs) toward the immune synapse between effector NK lymphocytes and target cells (PubMed : 24088571). In neurons, mediates the anterograde axonal long-range transport of presynaptic lysosome-related vesicles required for presynaptic biogenesis and synaptic function (By similarity). Also acts as a regulator of endosome to lysosome trafficking pathways of special significance for host defense (PubMed : 21802320). Recruits RUFY1 onto early endosomes regulating endosomes to trans-Golgi network proteins retrieval (PubMed : 36282215). Regulates cargo trafficking to lysosomes by binding to PLEKHM1 and recruiting the HOPS subunit VPS41, resulting in functional assembly of the HOPS complex on lysosomal membranes (PubMed : 16537643, PubMed : 25908847). Plays an important role in cargo delivery to lysosomes for antigen presentation and microbial killing. Directs the intersection of CD1d with lipid antigens in lysosomes, and plays a role in intersecting phagosomes with lysosomes to generate phagolysosomes that kill microbes (PubMed : 21802320, PubMed : 25908847). Involved in the process of MHC II presentation. Regulates the delivery of antigens to lysosomes and the formation of MHC II-peptide complexes through the recruitment of the HOPS complex to lysosomes allowing the fusion of late endosomes to lysosomes (By similarity). May play a role in chromosome segregation (PubMed : 15331635).. (Microbial infection) During Mycobacterium tuberculosis (Mtb) infection, is required for plasma membrane repair by controlling the exocytosis of lysosomes in macrophages. ARL8B secretion pathway is crucial to control the type of cell death of the M. tuberculosis-infected macrophages, distinguishing avirulent from virulent Mtb induced necrotic cell death.. (Microbial infection) During infection, coronaviruses such as SARS-CoV-2 and the chaperone HSPA5/GRP78 are probably co-released through ARL8B-dependent lysosomal exocytic pathway for unconventional egress.
See full target information ARL8B

Publications (3)

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

Nature chemical biology 21:577-587 PubMed39482469

2024

Carbonic anhydrase inhibition ameliorates tau toxicity via enhanced tau secretion.

Applications

Unspecified application

Species

Unspecified reactive species

Ana Lopez,Farah H Siddiqi,Julien Villeneuve,Rodrigo Portes Ureshino,Hee-Yeon Jeon,Philippos Koulousakis,Sophie Keeling,William A McEwan,Angeleen Fleming,David C Rubinsztein

Archives of toxicology 98:2695-2709 PubMed38769170

2024

Mechanistic screening of reproductive toxicity in a novel 3D testicular co-culture model shows significant impairments following exposure to low-dibutyl phthalate concentrations.

Applications

Unspecified application

Species

Unspecified reactive species

Radwa Almamoun,Paula Pierozan,Oskar Karlsson

Cell 183:1520-1535.e14 PubMed33157038

2020

β-Coronaviruses Use Lysosomes for Egress Instead of the Biosynthetic Secretory Pathway.

Applications

Unspecified application

Species

Unspecified reactive species

Sourish Ghosh,Teegan A Dellibovi-Ragheb,Adeline Kerviel,Eowyn Pak,Qi Qiu,Matthew Fisher,Peter M Takvorian,Christopher Bleck,Victor W Hsu,Anthony R Fehr,Stanley Perlman,Sooraj R Achar,Marco R Straus,Gary R Whittaker,Cornelis A M de Haan,John Kehrl,Grégoire Altan-Bonnet,Nihal Altan-Bonnet
View all publications

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