Thermo Fisher Scientific GPSM2 Polyclonal Antibody
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA5115322 | - | Thermo Fisher Scientific PA5115322 GPSM2 Polyclonal Antibody 100 ul pk | 재고문의 | pk | 657,000원 | - | 722,700원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1:1,000-1:3,000
Immunocytochemistry (ICC/IF)
1:100-1:500
Inhibition Assays (IA)
-
View 1 publication 1 publication
Product Specifications
Species Reactivity
Human, Mouse, Rat
Published species
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
A synthesized peptide derived from human GPSM2(Accession P81274), corresponding to amino acid residues M586-L636. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
GPSM2,
uniProtId:
P81274-1,
ncbiNodeId:
9606,
antigenRange:
586-636,
antigenLength:
684,
antigenImageFileName:
PA5-115322_GPSM2_P81274-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-115322_GPSM2_P81274-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
Purification
Affinity chromatography
Storage buffer
PBS with 50% glycerol
Contains
0.02% sodium azide
Storage conditions
-20°C
Shipping conditions
Wet ice
RRID
AB_2899958
Product Specific Information
Antibody detects endogenous levels of total GPSM2.
Target Information
The protein encoded by this gene belongs to a family of proteins that modulate activation of G proteins, which transduce extracellular signals received by cell surface receptors into integrated cellular responses. The N-terminal half of this protein contains 10 copies of leu-gly-asn repeat, and the C-terminal half contains 4 GoLoco motifs, which are involved in guanine nucleotide exchange. This protein may play a role in neuroblast division and in the development of normal hearing. Mutations in this gene are associated with autosomal recessive nonsyndromic deafness.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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