Mouse Anti-GNA11 Recombinant Antibody (CBLG1-3194) (CBMAB-G4050-LY)

This product is antibody recognizes GNA11. The antibody CBLG1-3194 immunoassay techniques such as: WB.
See all GNA11 antibodies

Datasheet

Summary

Host Animal

Mouse

Specificity

Mouse, Rat, Human

Clone

CBLG1-3194

Antibody Isotype

IgG

Application

Basic Information

Specificity

Mouse, Rat, Human

Antibody Isotype

IgG

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!]

Format

Liquid

Purity

> 95% Purity determined by SDS-PAGE.

Storage

Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.

Target

Full Name

guanine nucleotide binding protein, alpha 11

Introduction

The protein encoded by this gene belongs to the family of guanine nucleotide-binding proteins (G proteins), which function as modulators or transducers in various transmembrane signaling systems. G proteins are composed of 3 units: alpha, beta and gamma. This gene encodes one of the alpha subunits (subunit alpha-11). Mutations in this gene have been associated with hypocalciuric hypercalcemia type II (HHC2) and hypocalcemia dominant 2 (HYPOC2). Patients with HHC2 and HYPOC2 exhibit decreased or increased sensitivity, respectively, to changes in extracellular calcium concentrations. [provided by RefSeq, Dec 2013]

Entrez Gene ID

Human	2767
Mouse	14672
Rat	81662

UniProt ID

Human	P29992
Mouse	P21278
Rat	Q9JID2

Function

Guanine nucleotide-binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling systems. Acts as an activator of phospholipase C. Transduces FFAR4 signaling in response to long-chain fatty acids (LCFAs).

Biological Process

Action potential Source: GO_Central
Adenylate cyclase-modulating G protein-coupled receptor signaling pathway Source: GO_Central
Cellular response to pH Source: Ensembl
Developmental pigmentation Source: Ensembl
Entrainment of circadian clock Source: AgBase
G protein-coupled acetylcholine receptor signaling pathway Source: AgBase
Heart development Source: Ensembl
Phospholipase C-activating dopamine receptor signaling pathway Source: GO_Central
Phototransduction, visible light Source: AgBase
Regulation of melanocyte differentiation Source: Ensembl
Signal transduction Source: ProtInc
Skeletal system development Source: Ensembl

Cellular Location

Cell membrane; Cytoplasm. In testicular cells, expressed exclusively in the cytoplasm.

Involvement in disease

Hypocalciuric hypercalcemia, familial 2 (HHC2):
A form of hypocalciuric hypercalcemia, a disorder of mineral homeostasis that is transmitted as an autosomal dominant trait with a high degree of penetrance. It is characterized biochemically by lifelong elevation of serum calcium concentrations and is associated with inappropriately low urinary calcium excretion and a normal or mildly elevated circulating parathyroid hormone level. Hypermagnesemia is typically present. Affected individuals are usually asymptomatic and the disorder is considered benign. However, chondrocalcinosis and pancreatitis occur in some adults.
Hypocalcemia, autosomal dominant 2 (HYPOC2):
A form of hypocalcemia, a disorder of mineral homeostasis characterized by blood calcium levels below normal, and low or normal serum parathyroid hormone concentrations. Disease manifestations include hypocalcemia, paresthesias, carpopedal spasm, seizures, hypercalciuria with nephrocalcinosis or kidney stones, and ectopic and basal ganglia calcifications.

PTM

(Microbial infection) Deamidated at Gln-209 by Photorhabdus asymbiotica toxin PAU_02230, blocking GTP hydrolysis of heterotrimeric GNAQ or GNA11 and G-alphai (GNAI1, GNAI2 or GNAI3) proteins, thereby activating RhoA.

References

Hannan, F., Stevenson, M., Kooblall, K., Olesen, M., Yon, M., Stewart, M., ... & Thakker, R. (2022, October). Hypercalcaemic mice harbouring a germline ablation of G-protein subunit alpha-11 have anaemia that is corrected by treatment with erythropoietin. In Endocrine Abstracts (Vol. 86). Bioscientifica.

Zhang, H., Fu, T., & Zhang, C. (2021). MicroRNA-1249 targets G protein subunit alpha 11 and facilitates gastric Cancer cell proliferation, motility and represses cell apoptosis. OncoTargets and therapy, 14, 1249.

Gorvin, C. M., Stokes, V. J., Boon, H., Cranston, T., Glück, A. K., Bahl, S., ... & Thakker, R. V. (2020). Activating mutations of the G-protein subunit α 11 interdomain interface cause autosomal dominant hypocalcemia type 2. The Journal of Clinical Endocrinology & Metabolism, 105(3), 952-963.

Polubothu, S., Al-Olabi, L., Del Boente, M. C., Chacko, A., Eleftheriou, G., Glover, M., ... & Kinsler, V. A. (2020). GNA11 mutation as a cause of Sturge-Weber syndrome: expansion of the phenotypic spectrum of Gα/11 mosaicism and the associated clinical diagnoses. The Journal of Investigative Dermatology, 140(5), 1110.

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Protocols

Please try the standard protocols which include: protocols, troubleshooting and guide.

Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme Linked Immunospot (ELISpot)
Proteogenomic
Other Protocols

Associated Products

Isotype control

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

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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