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Mouse Anti-LRRC8A Recombinant Antibody (V2-60468) (CBMAB-L2137-YJ)

Provided herein is a Mouse monoclonal antibody, which binds to Leucine Rich Repeat Containing 8 Vrac Subunit A (LRRC8A). The antibody can be used for immunoassay techniques, such as ELISA, WB.
See all LRRC8A antibodies
Published Data

Summary

Host Animal
Mouse
Specificity
Human
Clone
V2-60468
Antibody Isotype
IgG2a, κ
Application
ELISA, WB

Basic Information

Immunogen
LRRC8A (NP_062540.2, 711 a.a. ~ 810 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.Immunogen sequence: QNLAITANRI ETLPPELFQC RKLRALHLGN NVLQSLPSRV GELTNLTQIE LRGNRLECLP VELGECPLLK RSGLVVEEDL FNTLPPEVKE RLWRADKEQA.
Specificity
Human
Antibody Isotype
IgG2a, κ
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Buffer
PBS, pH 7.4
Storage
Store at 4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.
Epitope
aa 711-810

Target

Full Name
leucine rich repeat containing 8 family, member A
Introduction
LRRC8A belongs to the leucine-rich repeat family of proteins, which function in diverse biological processes, including cell adhesion, cellular trafficking, and hormone-receptor interactions. This family member is a putative four-pass transmembrane protein that functions in B cell development. Defects in this gene cause autosomal dominant non-Bruton type agammaglobulinemia, an immunodeficiency disease resulting from defects in B cell maturation. Multiple alternatively spliced transcript variants, which encode the same protein, have been identified for this gene.
Entrez Gene ID
UniProt ID
Alternative Names
AGM5; LRRC8; SWELL1; volume-regulated anion channel subunit LRRC8A; leucine rich repeat containing 8 family member A; leucine-rich repeat-containing protein 8A; swelling protein 1
Function
Essential component of the volume-regulated anion channel (VRAC, also named VSOAC channel), an anion channel required to maintain a constant cell volume in response to extracellular or intracellular osmotic changes (PubMed:24725410, PubMed:29769723, PubMed:24790029, PubMed:26530471, PubMed:26824658, PubMed:28193731).
The VRAC channel conducts iodide better than chloride and can also conduct organic osmolytes like taurine (PubMed:24725410, PubMed:30095067, PubMed:24790029, PubMed:26530471, PubMed:26824658, PubMed:28193731).
Mediates efflux of amino acids, such as aspartate and glutamate, in response to osmotic stress (PubMed:28193731).
LRRC8A and LRRC8D are required for the uptake of the drug cisplatin (PubMed:26530471).
In complex with LRRC8C or LRRC8E, acts as a transporter of immunoreactive cyclic dinucleotide GMP-AMP (2'-3'-cGAMP), an immune messenger produced in response to DNA virus in the cytosol: mediates both import and export of 2'-3'-cGAMP, thereby promoting transfer of 2'-3'-cGAMP to bystander cells (PubMed:33171122).
In contrast, complexes containing LRRC8D inhibit transport of 2'-3'-cGAMP (PubMed:33171122).
Required for in vivo channel activity, together with at least one other family member (LRRC8B, LRRC8C, LRRC8D or LRRC8E); channel characteristics depend on the precise subunit composition (PubMed:24790029, PubMed:26824658, PubMed:28193731).
Can form functional channels by itself (in vitro) (PubMed:26824658).
Involved in B-cell development: required for the pro-B cell to pre-B cell transition (PubMed:14660746).
Also required for T-cell development (By similarity).
Required for myoblast differentiation: VRAC activity promotes membrane hyperpolarization and regulates insulin-stimulated glucose metabolism and oxygen consumption (By similarity).
Also acts as a regulator of glucose-sensing in pancreatic beta cells: VRAC currents, generated in response to hypotonicity- or glucose-induced beta cell swelling, depolarize cells, thereby causing electrical excitation, leading to increase glucose sensitivity and insulin secretion (PubMed:29371604).
Also plays a role in lysosome homeostasis by forming functional lysosomal VRAC channels in response to low cytoplasmic ionic strength condition: lysosomal VRAC channels are necessary for the formation of large lysosome-derived vacuoles, which store and then expel excess water to maintain cytosolic water homeostasis (PubMed:31270356, PubMed:33139539).
Biological Process
Anion transmembrane transportManual Assertion Based On ExperimentIDA:UniProtKB
Anion transportManual Assertion Based On ExperimentIMP:UniProtKB
Aspartate transmembrane transportIEA:Ensembl
Cell volume homeostasisManual Assertion Based On ExperimentIDA:UniProtKB
Cellular glucose homeostasisISS:UniProtKB
Chloride transmembrane transportManual Assertion Based On ExperimentIDA:UniProtKB
Cyclic-GMP-AMP transmembrane import across plasma membraneManual Assertion Based On ExperimentIDA:UniProtKB
Positive regulation of insulin secretionISS:UniProtKB
Positive regulation of myoblast differentiationISS:UniProtKB
Pre-B cell differentiationISS:UniProtKB
Protein hexamerizationManual Assertion Based On ExperimentIDA:UniProtKB
Response to osmotic stressManual Assertion Based On ExperimentIMP:UniProtKB
SpermatogenesisISS:UniProtKB
Taurine transportIEA:Ensembl
Cellular Location
Cell membrane
Lysosome membrane
Mainly localizes to the cell membrane, with some intracellular localization to lysosomes.
Involvement in disease
Agammaglobulinemia 5, autosomal dominant (AGM5):
A primary immunodeficiency characterized by profoundly low or absent serum antibodies and low or absent circulating B-cells due to an early block of B-cell development. Affected individuals develop severe infections in the first years of life.
Topology
Cytoplasmic: 1-23
Helical: 24-47
Extracellular: 48-123
Helical: 124-142
Cytoplasmic: 143-264
Helical: 265-286
Extracellular: 287-316
Helical: 317-341
Cytoplasmic: 342-810
PTM
N-glycosylated.

Rutz, S., Deneka, D., Dittmann, A., Sawicka, M., & Dutzler, R. (2023). Structure of a volume-regulated heteromeric LRRC8A/C channel. Nature Structural & Molecular Biology, 30(1), 52-61.

Kern, D. M., Bleier, J., Mukherjee, S., Hill, J. M., Kossiakoff, A. A., Isacoff, E. Y., & Brohawn, S. G. (2023). Structural basis for assembly and lipid-mediated gating of LRRC8A: C volume-regulated anion channels. Nature Structural & Molecular Biology, 1-12.

Yamada, T., Figueroa, E. E., Denton, J. S., & Strange, K. (2021). LRRC8A homohexameric channels poorly recapitulate VRAC regulation and pharmacology. American Journal of Physiology-Cell Physiology, 320(3), C293-C303.

Kurashima, K., Shiozaki, A., Kudou, M., Shimizu, H., Arita, T., Kosuga, T., ... & Otsuji, E. (2021). LRRC8A influences the growth of gastric cancer cells via the p53 signaling pathway. Gastric Cancer, 24, 1063-1075.

Serra, S. A., Stojakovic, P., Amat, R., Rubio-Moscardo, F., Latorre, P., Seisenbacher, G., ... & Posas, F. (2021). LRRC8A-containing chloride channel is crucial for cell volume recovery and survival under hypertonic conditions. Proceedings of the National Academy of Sciences, 118(23), e2025013118.

Lahey, L. J., Mardjuki, R. E., Wen, X., Hess, G. T., Ritchie, C., Carozza, J. A., ... & Li, L. (2020). LRRC8A: C/E heteromeric channels are ubiquitous transporters of cGAMP. Molecular cell, 80(4), 578-591.

Green, J. P., Swanton, T., Morris, L. V., El-Sharkawy, L. Y., Cook, J., Yu, S., ... & Brough, D. (2020). LRRC8A is essential for hypotonicity-, but not for DAMP-induced NLRP3 inflammasome activation. Elife, 9, e59704.

Konishi, T., Shiozaki, A., Kosuga, T., Kudou, M., Shoda, K., Arita, T., ... & Otsuji, E. (2019). LRRC8A expression influences growth of esophageal squamous cell carcinoma. The American Journal of Pathology, 189(10), 1973-1985.

Yang, C., He, L., Chen, G., Ning, Z., & Xia, Z. (2019). LRRC8A potentiates temozolomide sensitivity in glioma cells via activating mitochondria-dependent apoptotic pathway. Human Cell, 32, 41-50.

Formaggio, F., Saracino, E., Mola, M. G., Rao, S. B., Amiry-Moghaddam, M., Muccini, M., ... & Benfenati, V. (2019). LRRC8A is essential for swelling‐activated chloride current and for regulatory volume decrease in astrocytes. The FASEB Journal, 33(1), 101-113.

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For research use only. Not intended for any clinical use.

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