Thermo Fisher Scientific STX19 Polyclonal Antibody

Applications

Tested Dilution

Publications

Western Blot (WB)

0.04-0.4 µg/mL

-

Immunohistochemistry (Paraffin) (IHC (P))

1:50-1:200

-

Immunocytochemistry (ICC/IF)

0.25-2 µg/mL

-

Product Specifications

Species Reactivity

Human

Host/Isotype

Rabbit / IgG

Class

Polyclonal

Type

Antibody

Immunogen

Recombinant protein corresponding to Human STX19. Recombinant protein control fragment (Product #RP-95940). if (typeof window.$mangular === undefined || !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{targetFamily:STX19,uniProtId:Q8N4C7-1,ncbiNodeId:9606,antigenRange:13-153,antigenLength:294,antigenImageFileName:PA5-56519_STX19_Q8N4C7-1_Rabbit.svg,antigenImageFileNamePDP:PA5-56519_STX19_Q8N4C7-1_Rabbit_PDP.jpeg,sortOrder:1}\]; $mangular.isB2BCMGT = false; $mangular.isEpitopesModalImageMultiSizeEnabled = true;

View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

0.1 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_2648057

Product Specific Information

Immunogen sequence: KEIELSRDSH VSTTETEEQG VFLQQAVIYE REPVAERHLH EIQKLQESIN NLADNVQKFG QQQKSLVASM RRFSLLKRES TITKEIKIQA EYINRSLNDL VKEVKKSEVE NGPSSVVTRI LKSQHAAMFR HFQQIMFIYN D

Highest antigen sequence identity to the following orthologs: Mouse - 82%, Rat - 30%.

Target Information

Syntaxin 19, also known as STX19, is a 294 amino acid peripheral membrane protein that contains one t-SNARE coiled-coil homology domain and belongs to the syntaxin family, suggesting a role in synaptic vesicle fusion. The gene encoding Syntaxin 19 maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.