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  • KD/KO Validated

GPSM2 Polyclonal antibody

GPSM2 Polyclonal Antibody for ELISA
Cat No. 11608-2-AP

Host / Isotype

Rabbit / IgG

Reactivity

human and More (1)

Applications

WB, IHC, IF, IP, ELISA

GPSM2, LGN, Mosaic protein LGN, Pins

Formulation:  PBS and Azide
PBS and Azide
Conjugate:  Unconjugated
Size/Concentration: 

-/ -


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国内在庫・納期について

約2万点のプロテインテック製品をコスモバイオ社物流センター(国内)に在庫しています。国内在庫の有無はコスモバイオ社ホームページの「品番検索」でカタログ番号を検索して確認できます。


保証・サポートについて

テクニカルサポートまたはご購入後1年間の交換/補填対応を承ります。詳細はこちらをご覧ください。


Tested Applications

Recommended dilution

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.

Product Information

11608-2-AP targets GPSM2 in WB, IHC, IF, IP, ELISA applications and shows reactivity with human samples.

Tested Reactivity human
Cited Reactivityhuman, mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen GPSM2 fusion protein Ag2167 相同性解析による交差性が予測される生物種
Full Name G-protein signaling modulator 2 (AGS3-like, C. elegans)
Calculated molecular weight 75 kDa
GenBank accession numberBC027732
Gene Symbol GPSM2
Gene ID (NCBI) 29899
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
UNIPROT IDP81274
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol , pH 7.3
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

Background Information

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
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