Thermo Fisher Scientific GCNT1 Polyclonal Antibody
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Applications
Tested Dilution
Publications
Immunohistochemistry (Paraffin) (IHC (P))
1:50-1:200
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant protein corresponding to Human GCNT1. Recombinant protein control fragment (Product #RP-102176). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
GCNT1,
uniProtId:
Q02742-1,
ncbiNodeId:
9606,
antigenRange:
213-324,
antigenLength:
428,
antigenImageFileName:
PA5-56657_GCNT1_Q02742-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-56657_GCNT1_Q02742-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.05 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
PBS, pH 7.2, with 40% glycerol
Contains
0.02% sodium azide
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Wet ice
RRID
AB_2641918
Product Specific Information
Immunogen sequence: LINLCGMDFP IKTNLEIVRK LKLLMGENNL ETERMPSHKE ERWKKRYEVV NGKLTNTGTV KMLPPLETPL FSGSAYFVVS REYVGYVLQN EKIQKLMEWA QDTYSPDEYL WA
Highest antigen sequence identity to the following orthologs: Mouse - 86%, Rat - 83%.
Target Information
Glycosylation is one of the most universal but at the same time complex protein modifications. Modification with sugar moeties can be both co- translational and post- translational, occurring in the endoplasmatic reticulum and golgi. Three different forms of glycosylation can be distinguished: N-linked oligosaccharides, O-linked oligosaccharides and glycosyl- phosphatidylinositol (GPI-) anchors. Glycosylation results in thousands of distinct, bioactive glycoproteins resident throughout the cell that strongly determine protein-protein, carbohydrate-protein, membrane, and adhesion properties. Diseases associated with glycosylation defects include Congenital disorders of glycosylation, (CDG), also known as carbohydrate deficient glycoprotein syndromes, and diseases associated with advanced aging.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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