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AB74142

Anti-RhoGDI (phospho S174) antibody

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(3 Publications)

Rabbit Polyclonal RhoGDI phospho S174 antibody. Suitable for WB, IHC-P and reacts with Human samples. Cited in 3 publications. Immunogen corresponding to Synthetic Peptide within Human ARHGDIA phospho S174.

View Alternative Names

GDIA1, ARHGDIA, Rho GDP-dissociation inhibitor 1, Rho GDI 1, Rho-GDI alpha

2 Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-RhoGDI (phospho S174) antibody (AB74142)
  • IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-RhoGDI (phospho S174) antibody (AB74142)

Human cervix carcinoma tissue stained with ab74142 (1/50 dilution).
1 : No phosphopeptide
2 : Phosphopeptide

Western blot - Anti-RhoGDI (phospho S174) antibody (AB74142)
  • WB

Unknown

Western blot - Anti-RhoGDI (phospho S174) antibody (AB74142)

All lanes:

Western blot - Anti-RhoGDI (phospho S174) antibody (ab74142) at 1/500 dilution

Lane 1:

HUVEC cells treated with EGF (200ng/ml, 30mins) at 30 µg

Lane 2:

HUVEC cells treated with EGF (200ng/ml, 30mins) at 30 µg with phosphopeptide

Predicted band size: 23 kDa

Observed band size: 105 kDa,23 kDa,60 kDa

false

Key facts

Host species

Rabbit

Clonality

Polyclonal

Isotype

IgG

Carrier free

No

Reacts with

Human

Applications

IHC-P, WB

applications

Immunogen

Synthetic Peptide within Human ARHGDIA phospho S174. The exact immunogen used to generate this antibody is proprietary information.

P52565

Reactivity data

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Properties and storage information

Form
Liquid
Purification technique
Affinity purification Immunogen
Purification notes
The antibody was purified by affinity chromatography using epitope specific phosphopeptide. The antibody against non phosphopeptide was removed by chromatography using non phosphopeptide corresponding to the phosphorylation site.
Storage buffer
pH: 7.4 Preservative: 0.02% Sodium azide Constituents: PBS, 50% Glycerol (glycerin, glycerine), 0.87% Sodium chloride
Shipped at conditions
Blue Ice
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.

RhoGDI also known as Rho GDP-dissociation inhibitor 1 is a regulatory protein with a mass of approximately 23 kDa. It primarily inhibits the dissociation of GDP from Rho GTPases such as RhoA Rac1 and Cdc42. This protein plays an important role in controlling the cycling between active GTP-bound and inactive GDP-bound states of small GTPases. RhoGDI shows expression in numerous tissues highlighting its widespread regulatory functions in cell signaling.
Biological function summary

RhoGDI modulates the activity of Rho family GTPases—a group responsible for organizing the actin cytoskeleton which determines cell shape polarity and movement. It does not operate alone; rather it is part of a complex with membrane-bound and cytosolic proteins offering a shuttle service to balance GTPases between cellular locations. By doing so RhoGDI influences processes like cell migration and the cell cycle integral to maintaining proper cellular architecture.

Pathways

Scientists recognize RhoGDI’s participation in key signaling pathways particularly the Rho GTPase cycle and actin cytoskeleton organization. It interacts with proteins like ROCK and PAK within these pathways to achieve precise control of cytoskeletal dynamics. RhoGDI coordinates with these proteins to play a central role in cellular responses to external stimuli impacting processes like wound healing and cellular development.

RhoGDI has associations with cancer and neurodegenerative diseases. Its deregulation can disrupt the Rho GTPase pathways leading to uncontrolled cell proliferation in cancers such as breast and prostate cancer. Additionally altered RhoGDI function affects neuronal growth and survival linking it to neurodegenerative conditions like Alzheimer’s disease. Within these contexts RhoGDI interacts with other proteins such as Rac1 and Cdc42 to influence disease progression and pathology.

Product protocols

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

Target data

Controls Rho proteins homeostasis. Regulates the GDP/GTP exchange reaction of the Rho proteins by inhibiting the dissociation of GDP from them, and the subsequent binding of GTP to them. Retains Rho proteins such as CDC42, RAC1 and RHOA in an inactive cytosolic pool, regulating their stability and protecting them from degradation. Actively involved in the recycling and distribution of activated Rho GTPases in the cell, mediates extraction from membranes of both inactive and activated molecules due its exceptionally high affinity for prenylated forms. Through the modulation of Rho proteins, may play a role in cell motility regulation. In glioma cells, inhibits cell migration and invasion by mediating the signals of SEMA5A and PLXNB3 that lead to inactivation of RAC1.
See full target information ARHGDIA phospho S174

Publications (3)

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

Biomedicines 13: PubMed40149625

2025

Gastrodin Mitigates Ketamine-Induced Inhibition of F-Actin Remodeling and Cell Migration by Regulating the Rho Signaling Pathway.

Applications

Unspecified application

Species

Unspecified reactive species

Ping-Cheng Shih,I-Shiang Tzeng,Yi-Chyan Chen,Mao-Liang Chen

PloS one 12:e0187094 PubMed29121646

2017

The phosphomimetic mutation of syndecan-4 binds and inhibits Tiam1 modulating Rac1 activity in PDZ interaction-dependent manner.

Applications

Unspecified application

Species

Unspecified reactive species

Aniko Keller-Pinter,Bettina Ughy,Monika Domoki,Aladar Pettko-Szandtner,Tamas Letoha,Jozsef Tovari,Jozsef Timar,Laszlo Szilak

The Journal of biological chemistry 287:38705-15 PubMed23012358

2012

Regulation of RhoA signaling by the cAMP-dependent phosphorylation of RhoGDIα.

Applications

WB

Species

Unspecified reactive species

Atsuro Oishi,Noriko Makita,Junichiro Sato,Taroh Iiri
View all publications

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