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Merck
모든 사진(2)

주요 문서

810206P

Avanti

NBD Sphinganine

omega(7-nitro-2-1,3-benzoxadiazol-4-yl)(2S,3R)-2-aminooctadecane-1,3-diol, powder

동의어(들):

D-erythro-sphinganine-N-NBD; NBD-dihydrosphingosine

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모든 사진(2)

About This Item

실험식(Hill 표기법):
C24H41N5O5
CAS Number:
1246303-03-6
Molecular Weight:
479.61
UNSPSC 코드:
12352211
NACRES:
NA.25

분석

>99% (TLC)

형태

powder

포장

pkg of 1 × 100 μg ((810206P-100UG))
pkg of 1 × 250 μg (810206P-250ug)
pkg of 1 × 50 μg (810206P-50UG)

제조업체/상표

Avanti Research™ - A Croda Brand 810206P

배송 상태

dry ice

저장 온도

−20°C

일반 설명

Sphinganine, also called as dihydrosphingosine is a common sphingoid base in phospholipids.

애플리케이션

NBD Sphinganine or omega (7-nitro-2-1,3-benzoxadiazol-4-yl)(2S,3R)-2-aminooctadecane-1,3-diol is suitable for the analysis of the dihydrosphingosine (DHS) localization to endoplasmic reticulum for the activation of activating transcription factor 6 (ATF6) protein.
NBD Sphinganine or omega(7-nitro-2-1,3-benzoxadiazol-4-yl)(2S,3R)-2-aminooctadecane-1,3-diol is suitable for the analysis of the dihydrosphingosine (DHS) localization to endoplasmic reticulum for the activation of activating transcription factor 6 (ATF6) protein.

포장

5 mL Amber Glass Screw Cap Vial (810206P-100UG)
5 mL Amber Glass Screw Cap Vial (810206P-250UG)
5ML Glass Amber Screw Cap Vial (810206P-50UG)

법적 정보

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

No data available

Flash Point (°C)

No data available

시험 성적서(COA)

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문서 라이브러리 방문

Arvin B Tam et al.
Developmental cell, 46(3), 327-343 (2018-08-08)
The unfolded protein response (UPR) is induced by proteotoxic stress of the endoplasmic reticulum (ER). Here we report that ATF6, a major mammalian UPR sensor, is also activated by specific sphingolipids, dihydrosphingosine (DHS) and dihydroceramide (DHC). Single mutations in a previously
Junliang Wan et al.
Journal of agricultural and food chemistry, 67(46), 12953-12961 (2019-10-23)
Most common sphingolipids are comprised of "typical" sphingoid bases (sphinganine, sphingosine, and structurally related compounds) and are produced via the condensation of l-serine with a fatty acyl-CoA by serine palmitoyltransferase. Some organisms, including mammals, also produce "atypical" sphingoid bases that

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