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Merck
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MABF270

Sigma-Aldrich

Anti-STING Antibody, clone S17G2C4B7

clone S17G2C4B7, from mouse

Szinonimák:

Stimulator of interferon genes protein, Endoplasmic reticulum interferon stimulator, ERIS, hMITA, hSTING, Mediator of IRF3 activation, Transmembrane protein 173

Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez


About This Item

UNSPSC kód:
12352203
eCl@ss:
32160702
NACRES:
NA.41
klón:
S17G2C4B7, monoclonal
application:
ICC
WB
faj reaktivitás:
mouse, human
technika/technikák:
immunocytochemistry: suitable
western blot: suitable
citations:
4

biológiai forrás

mouse

Minőségi szint

antitest forma

purified antibody

antitest terméktípus

primary antibodies

klón

S17G2C4B7, monoclonal

faj reaktivitás

mouse, human

technika/technikák

immunocytochemistry: suitable
western blot: suitable

izotípus

IgG1κ

NCBI elérési szám

UniProt elérési szám

kiszállítva

wet ice

célzott transzláció utáni módosítás

unmodified

Géninformáció

Általános leírás

Stimulator of interferon genes protein (UniProt Q86WV6; also known as Endoplasmic reticulum interferon stimulator, ERIS, hMITA, hSTING, Mediator of IRF3 activation, Transmembrane protein 173) is encoded by the TMEM173 (also known as ERIS, MITA, MPYS, SAVI, STING) gene (Gene ID 340061) in human. STING is an adaptor protein activated by cytosolic dsDNA or cyclic dinucleotides and plays a critical role in initiating innate responses to infection by various pathogens, including Herpes simplex virus (HSV). Once activated, STING translocates to the endoplasmic reticulum and activates the TBK1/IRF3 pathway that in turn mediates the upregulation of interferon (IFN) β. In addition, the DNA sensor IFI16 is also known to function as a STING ligand and potentiates STING-dependent sensing of viral infection by presenting cellular viral DNA to STING. STING is a four transmembrane (a.a. 21-41, 47-67, 87-106, 116-136) protein with both its N- and C-terminal ends exposed intracellularly (a.a. 1-20 and 137-379).The C-terminal cytoplasmic tail contains the c-di-GMP-binding domain (CBD; a.a. 153-340) with two c-di-GMP-binding regions (a.a. 162-167 & 238-241).

Egyediség

Clone S17G2C4B7 recognizes an epitope in the C-terminal cytoplasmic domain of human and murine STING.

Immunogén

Epitope: Amino acids 301-315.
His-tagged recombinant human STING C-terminal cytoplasmic domain fragment.

Alkalmazás

Anti-STING Antibody, clone S17G2C4B7 is an antibody against STING for use in Western Blotting, Immunocytochemistry.
Research Category
Inflammation & Immunology
Research Sub Category
Infectious Diseases - Viral
Western Blotting Analysis: A 1:200 dilution from a representative lot detected the expression of exogenously transfected human and murine STING in HEK293T cells, as well as the endogenous STING in telomerase-immortalized human foreskin fibroblasts hTERT-BJ1 (Courtesy of Dr. Glen N. Barber, University of Miami School of Medicine, FL, U.S.A.).
Immunocytochemistry Analysis: A 1:50 dilution from a representative lot detected the expression of exogenously transfected human and murine STING in HEK293T cells, as well as the endogenous STING in telomerase-immortalized human foreskin fibroblasts hTERT-BJ1 (Courtesy of Dr. Glen N. Barber, University of Miami School of Medicine, FL, U.S.A.).

Minőség

Evaluated by Western Blotting in HEK293T cell lysate.

Western Blotting Analysis: 1.0 µg/mL of this antibody detected STING in 50 µg of HEK293T cell lysate.

Cél megnevezése

~38 kDa observed. 42.19 kDa calculated.

Fizikai forma

Format: Purified
Protein G Purified
Purified mouse monoclonal IgG1κ antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Tárolás és stabilitás

Stable for 1 year at 2-8°C from date of receipt.

Egyéb megjegyzések

Concentration: Please refer to lot specific datasheet.

Jogi nyilatkozat

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Tárolási osztály kódja

12 - Non Combustible Liquids

WGK

WGK 1

Lobbanási pont (F)

Not applicable

Lobbanási pont (C)

Not applicable


Analitikai tanúsítványok (COA)

Analitikai tanúsítványok (COA) keresése a termék sarzs-/tételszámának megadásával. A sarzs- és tételszámok a termék címkéjén találhatók, a „Lot” vagy „Batch” szavak után.

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Az Ön által nemrégiben megvásárolt termékekre vonatkozó dokumentumokat a Dokumentumtárban találja.

Dokumentumtár megtekintése

Guoqiang Zhu et al.
Journal of virology, 97(5), e0022823-e0022823 (2023-05-10)
African swine fever (ASF), caused by the African swine fever virus (ASFV), is a transboundary infectious disease of domestic pigs and wild boars, resulting in significant swine production losses. Currently, no effective commercial ASF vaccines or therapeutic options are available.
Tanusree Sen et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 40(2), 424-446 (2019-11-07)
Persistent endoplasmic reticulum (ER) stress in neurons is associated with activation of inflammatory cells and subsequent neuroinflammation following traumatic brain injury (TBI); however, the underlying mechanism remains elusive. We found that induction of neuronal-ER stress, which was mostly characterized by
Dapei Li et al.
The Journal of biological chemistry, 297(2), 100930-100930 (2021-07-04)
Interferon-γ-inducible factor 16 (IFI16) triggers stimulator of interferon (IFN) genes (STING)-dependent type I IFN production during host antiviral immunity and facilitates p53-dependent apoptosis during suppressing tumorigenesis. We have previously reported that STING-mediated IFI16 degradation negatively regulates type I IFN production.
Liyong Zhang et al.
Nature cardiovascular research, 1(12), 1195-1214 (2022-12-01)
Heart failure (HF) is a rising global cardiovascular epidemic driven by aging and chronic inflammation. As elderly populations continue to increase, precision treatments for age-related cardiac decline are urgently needed. Here we report that cardiac and blood expression of IGFBP7

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