• Phare
  • Validé par KD/KO

Anticorps Polyclonal de lapin anti-GPSM2

GPSM2 Polyclonal Antibody for ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain et plus (1)

Applications

WB, IHC, IF,ELISA

Conjugaison

Non conjugué

N° de cat : 11608-2-AP

Synonymes

GPSM2, LGN, Mosaic protein LGN, Pins



Applications testées

Dilution recommandée

ApplicationDilution
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, check data in validation data gallery

Informations sur le produit

11608-2-AP cible GPSM2 dans les applications de WB, IHC, IF,ELISA et montre une réactivité avec des échantillons Humain

Réactivité Humain
Réactivité citéeHumain, souris
Hôte / Isotype Lapin / IgG
Clonalité Polyclonal
Type Anticorps
Immunogène GPSM2 Protéine recombinante Ag2167
Nom complet G-protein signaling modulator 2 (AGS3-like, C. elegans)
Masse moléculaire calculée 75 kDa
Numéro d’acquisition GenBankBC027732
Symbole du gène GPSM2
Identification du gène (NCBI) 29899
Conjugaison Non conjugué
Forme Liquide
Méthode de purification Purification par affinité contre l'antigène
Tampon de stockage PBS avec azoture de sodium à 0,02 % et glycérol à 50 % pH 7,3
Conditions de stockageStocker à -20°C. Stable pendant un an après l'expédition. L'aliquotage n'est pas nécessaire pour le stockage à -20oC Les 20ul contiennent 0,1% de BSA.

Informations générales

GPSM2 belongs to a family of proteins that modulate activation of G proteins. GPSM2 assists in the exchange of guanine nucleotides, and allows extracellular signals to be transmitted to cells via cell surface, and ultimately plays a key role in the activation of G-proteins. Therefore, GPSM2 is a critical factor for the stability of cell division. Some recent studies have shown that GPSM2 messenger RNA (mRNA) is overexpressed and plays a positive role in the development of certain tumors, such as liver cancer, pancreatic cancer, breast cancer. It also plays a role in neuroblast division and in the development of normal hearing. Mutations in GPSM2 are associated with autosomal recessive nonsyndromic deafness (DFNB82), which is a form of non-syndromic deafness characterized by prelingual, bilateral, severe, sensorineural hearing loss.

Publications

SpeciesApplicationTitle
mouseIHC,IF

Am J Hum Genet

Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82.

Authors - Walsh Tom T
mouseWB

Cell Res

Pins homolog LGN regulates meiotic spindle organization in mouse oocytes.

Authors - Guo Xinzheng X
mouseIF

Sci Rep

Deletion of Brg1 causes abnormal hair cell planer polarity, hair cell anchorage, and scar formation in mouse cochlea.

Authors - Yecheng Jin
mouseWB

Mol Biol Cell

NuMA localization, stability, and function in spindle orientation involve 4.1 and Cdk1 interactions.

Authors - Seldin Lindsey L
humanWB

Genes Chromosomes Cancer

Critical roles of LGN/GPSM2 phosphorylation by PBK/TOPK in cell division of breast cancer cells.

Authors - Fukukawa Chikako C
  • KD Validated
mouseIF

Mamm Genome

The GPSM2/LGN GoLoco motifs are essential for hearing.

Authors - Yoni Bhonker