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Recombinant Human GNA11 Protein, N-His

Catalog #:   YHD85801 Specific References (49) DATASHEET
Applications: ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Expression system: E. coli
Accession: P29992
Protein length: Met1-Val359
Overview

Catalog No.

YHD85801

Expression system

E. coli

Species

Homo sapiens (Human)

Protein length

Met1-Val359

Predicted molecular weight

44.43 kDa

Nature

Recombinant

Endotoxin level

Please contact with the lab for this information.

Purity

>90% as determined by SDS-PAGE.

Accession

P29992

Applications

ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress

Form

Lyophilized

Storage buffer

Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.

Reconstitution

Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.

Shipping

In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.

Stability and Storage

Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.

Alternative Names

G-protein subunit alpha-11, Guanine nucleotide-binding protein G(y) subunit alpha, GNA11, G alpha-11, GA11, Guanine nucleotide-binding protein subunit alpha-11

Data Image
  • SDS-PAGE
    SDS PAGE for recombinant Human GNA11 protein
References

Iris and anterior chamber angle melanoma masquerading as benign melanocytic lesion., PMID:40491523

Presence of tumor DNA in aqueous humor is correlated with high risk uveal melanoma., PMID:40461505

Case report: Clinical and genetic characteristics of heterozygous CaSR variants in three Chinese females with familial hypocalciuric hypercalcemia type 1: a report of three cases., PMID:40417236

Short Report: The Variants in CHEK2 in Metastatic Uveal Melanoma., PMID:40283643

Co-occurrence of EIF1AX, SF3B1, or BAP1 variants in uveal melanomas: A case series and review., PMID:40271082

Segmental Congenital Vascular Anomaly With Atrophy, Ulceration and Scarring With Complications in Pregnancy., PMID:40019051

A novel FTO-targeting nanodrug induces disulfidptosis and ameliorates the suppressive tumor immune environment to treat uveal melanoma., PMID:40015005

Functional-proteomics-based investigation of the cellular response to farnesyltransferase inhibition in lung cancer., PMID:39995872

Gαq/11 aggravates acute lung injury in mice by promoting endoplasmic reticulum stress-mediated NETosis., PMID:39972252

[Research progress of GNAQ/GNA11-related capillary malformation spectrum]., PMID:39938999

Co-isolation of human donor eye cells and development of oncogene-mutated melanocytes to study uveal melanoma., PMID:39838458

An activating calcium-sensing receptor variant with biased signaling reveals a critical residue for Gα11 coupling., PMID:39658204

Phenotypic Spectrum of GNA11 R183C Mosaicism., PMID:39654261

Treatment sequence with tebentafusp and immune checkpoint inhibitors in patients with metastatic uveal melanoma and metastatic GNA11/GNAQ mutant melanocytic tumors., PMID:39647344

Gq/G11 oncogenic mutations promote PD-L1 expression and suppress tumor immunity., PMID:39550833

CYSLTR1 antagonism displays potent anti-tumor effects in uveal melanoma., PMID:39389443

Persistent Thrombotic Hemangioma With Organizing/Anastomosing Features: A Case Report of a Guanine Nucleotide-Binding Protein Alpha Subunit (GNA)-Mutated Cutaneous Vascular Lesion., PMID:39360118

[Uveal Melanoma: Molecular and Genetic Mechanisms of Development and Therapeutic Approaches]., PMID:39355878

Pathogenic Germline Variants in Uveal Melanoma Driver and BAP1-Associated Genes in Finnish Patients with Uveal Melanoma., PMID:39344744

Malignant blue melanoma., PMID:39260463

Genomic landscape of cutaneous, acral, mucosal, and uveal melanoma in Japan: analysis of clinical comprehensive genomic profiling data., PMID:39249554

[Familial Hypocalciuric Hypercalcemia Type 1 Likely Secondary to a New Inactivating Mutation of CASR]., PMID:39243411

NRASQ61R-driven atypical melanocytic tumor with blue nevus-like morphology: A case report., PMID:39177027

Familial hypocalciuric hypercalcemia in an infant: diagnosis and management quandaries., PMID:39163488

Protein and mRNA Expression in Uveal Melanoma Cell Lines Are Related to GNA and BAP1 Mutation Status., PMID:39042403

RhoA-mediated G12-G13 signaling maintains muscle stem cell quiescence and prevents stem cell loss., PMID:39009565

Delineation of the phenotypes and genotypes of PIK3CA-related overgrowth spectrum in East asians., PMID:38980418

Loss-of-function Thr347Ala Variant in the G Protein Subunit-Α11 Causes Familial Hypocalciuric Hypercalcemia 2., PMID:38920275

Somatic GNA11/GNAQ variants in a cohort of Chinese children with phakomatosis pigmentovascularis., PMID:38910853

Clinical and genetic characteristics of BAP1-mutated non-uveal and uveal melanoma., PMID:38903495

Molecularly matched targeted therapy: a promising approach for refractory metastatic melanoma., PMID:38761384

Utility of next-generation sequencing in the diagnosis of metastatic melanoma: A case report., PMID:38757469

[Circumscribed choroidal hemangioma and non-pigmented choroidal melanoma: clinical, instrumental and molecular genetic features]., PMID:38742493

A Phase II Study of ERK Inhibition by Ulixertinib (BVD-523) in Metastatic Uveal Melanoma., PMID:38683104

Identification and validation of a costimulatory molecule-related signature to predict the prognosis for uveal melanoma patients., PMID:38644411

Gα11 deficiency increases fibroblast growth factor 23 levels in a mouse model of familial hypocalciuric hypercalcemia., PMID:38530370

Double somatic mutations in CTNNB1 and GNA11 in an aldosterone-producing adenoma., PMID:38505749

Identification and characterization of a novel CASR mutation causing familial hypocalciuric hypercalcemia., PMID:38487341

EHMT2 promotes tumorigenesis in GNAQ/11-mutant uveal melanoma via ARHGAP29-mediated RhoA pathway., PMID:38486999

Molecular Frontiers in Melanoma: Pathogenesis, Diagnosis, and Therapeutic Advances., PMID:38474231

Somatic Loss-of-Function PIK3R1 and Activating Non-hotspot PIK3CA Mutations Associated with Capillary Malformation with Dilated Veins (CMDV)., PMID:38431221

PKC-independent PI3K signalling diminishes PKC inhibitor sensitivity in uveal melanoma., PMID:38418838

Emerging therapeutic strategies for metastatic uveal melanoma: Targeting driver mutations., PMID:38411373

Mass Spectrometry-Based Profiling of Histone Post-Translational Modifications in Uveal Melanoma Tissues, Human Melanocytes, and Uveal Melanoma Cell Lines - A Pilot Study., PMID:38349785

Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants., PMID:38321651

Clinical and Genomic Predictors of Adverse Events in Newly Diagnosed Glioblastoma., PMID:38252427

Cooperative function of oncogenic MAPK signaling and the loss of Pten for melanoma migration through the formation of lamellipodia., PMID:38233537

INPP5A phosphatase is a synthetic lethal target in GNAQ and GNA11-mutant melanomas., PMID:38233483

Discovery of Darovasertib (NVP-LXS196), a Pan-PKC Inhibitor for the Treatment of Metastatic Uveal Melanoma., PMID:38198520

Datasheet
$ 313
Product specifications
100 μg 313 1 mg 1629

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For research use only. Not for human or drug use.

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Recombinant Human GNA11 Protein, N-His [YHD85801]
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