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Anti-G-protein coupled receptor 56 (GPR56) Antibody, clone H11

clone H11, from mouse

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Synonym(s):
G protein-coupled receptor 56, 7-transmembrane protein with no EGF-like N-terminal domains-1, Protein TM7XN1, G-protein coupled receptor 56
eCl@ss:
32160702
NACRES:
NA.41

biological source

mouse

Quality Level

antibody form

purified antibody

antibody product type

primary antibodies

clone

H11, monoclonal

species reactivity

mouse

species reactivity (predicted by homology)

human (based on 100% sequence homology)

technique(s)

immunocytochemistry: suitable
immunohistochemistry: suitable
western blot: suitable

isotype

IgG1κ

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Gene Information

human ... GPR56(9289)

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This Item
ABS1028SAB1401465SAB4503610
antibody form

purified antibody

antibody form

affinity isolated antibody

antibody form

purified immunoglobulin

antibody form

affinity isolated antibody

clone

H11, monoclonal

clone

polyclonal

clone

polyclonal

clone

polyclonal

species reactivity

mouse

species reactivity

rat, human

species reactivity

human

species reactivity

human

technique(s)

immunocytochemistry: suitable, immunohistochemistry: suitable, western blot: suitable

technique(s)

immunocytochemistry: suitable, immunoprecipitation (IP): suitable, western blot: suitable

technique(s)

western blot: 1 μg/mL

technique(s)

ELISA: 1:20000, immunofluorescence: 1:100-1:500, western blot: 1:500-1:1000

isotype

IgG1κ

isotype

-

isotype

-

isotype

-

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General description

G-protein coupled receptor 56 (GPR56) is a ubiquitous adhesion receptor, which belongs to the G-protein coupled receptor 2 family and LN-TM7 subfamily. It is abundantly expressed in the in thyroid gland, brain, heart, and various tumor cells. Previous studies have suggested that GPR56 may inhibit the progression and metastasis of melanomas by interaction with extracellular-matrix proteins, such as Tissue Transglutaminase. GPR56 also plays a role in regulating VEGF production and angiogenesis via a PKCα-mediated pathway. GPR56 also plays a critical role in the development of the frontal cortex; previous studies have reported that mutations in GPR56 result in disorganized cortical lamination, which is most pronounced in the frontal cortex. This condition is known as bilateral frontoparietal polymicrogyria or BFPP.

Immunogen

N-terminal fragment of mouse GPR56

Application

Immunohistochemistry Analysis: A representative lot was used by an independent laboratory in E14.5 mouse brain tissue. (Luo, R., et al. (2011). Proc Natl Acad Sci U S A. 108(31):12925-12930.)

Immunocytochemistry Analysis: A representative lot was used by an independent laboratory in meningeal fibroblasts (MFs). (Luo, R., et al. (2011). Proc Natl Acad Sci U S A. 108(31):12925-12930.)
Research Category
Neuroscience
Research Sub Category
Adhesion (CAMs)
This Anti-G-protein coupled receptor 56 (GPR56) Antibody, clone H11 is validated for use in Western Blotting, ICC, IHC for the detection of G-protein coupled receptor 56 (GPR56).

Quality

Evaluated by Western Blot in brain tissue lysate from E13-E14 mouse.

Western Blot Analysis: 0.5 μg/mL of this antibody detected G-protein coupled receptor 56 in 10 µg of brain tissue lysate from E13-E14 mouse.

Target description

~62 kDa observed. Full-length GPR56 (GPR56FL) migrates at 75 kDa and the cleaved extracellular domain of GPR56 (GPR56ECD) migrates at 62 kDa (J Biol Chem. 2008 May 23;283(21):14469-78).

Physical form

Format: Purified
Protein G Purified
Purified mouse monoclonal IgG1κ in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Storage and Stability

Stable for 1 year at 2-8°C from date of receipt.

Analysis Note

Control
Brain tissue lysate from E13-E14 mouse

Other Notes

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Oladapo E Olaniru et al.
Molecular metabolism, 53, 101285-101285 (2021-07-06)
Members of the adhesion G protein-coupled receptor (aGPCR) subfamily are important actors in metabolic processes, with GPR56 (ADGRG1) emerging as a possible target for type 2 diabetes therapy. GPR56 can be activated by collagen III, its endogenous ligand, and by
D Daria et al.
Leukemia, 30(8), 1734-1741 (2016-04-12)
The G protein-coupled receptor 56 (GPR56) was identified as part of the molecular signature of functionally validated leukemic stem cells isolated from patients with acute myeloid leukemia (AML). This report now demonstrates particularly high expression of GPR56 in patients with
Gabriel S Salzman et al.
Proceedings of the National Academy of Sciences of the United States of America, 114(38), 10095-10100 (2017-09-07)
Adhesion G protein-coupled receptors (aGPCRs) play critical roles in diverse biological processes, including neurodevelopment and cancer progression. aGPCRs are characterized by large and diverse extracellular regions (ECRs) that are autoproteolytically cleaved from their membrane-embedded signaling domains. Although ECRs regulate receptor
Ayako Y Murayama et al.
Scientific reports, 10(1), 21516-21516 (2020-12-11)
GPR56, a member of the adhesion G protein-coupled receptor family, is abundantly expressed in cells of the developing cerebral cortex, including neural progenitor cells and developing neurons. The human GPR56 gene has multiple presumptive promoters that drive the expression of
Shih-Chia Huang et al.
EMBO molecular medicine, 9(12), 1660-1680 (2017-10-11)
Lymph node (LN) metastasis is commonly associated with systemic distant organ metastasis in human breast cancer and is an important prognostic predictor for survival of breast cancer patients. However, whether tumor-draining LNs (TDLNs) play a significant role in modulating the

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