Cat. Number |
1536
|
Chemical Name |
N-ʮ-D3-֬뮴 N-Octadecanoyl-D3-sulfatide, deuterated, 1mg
|
Mol. Formula |
C42H78D3NO11S
|
Mol. Weight |
811
|
Qty 1 |
1mg
|
Appearance |
solid
|
Application Notes |
98+%,TLC; identity confirmed by MS
|
Synonym |
N-C18:0-CD3-Sulfatide; N-Stearoyl-CD3-sulfatide
|
Solubility |
chloroform/methanol/DI water, 2:1:0.1
|
Storage condition |
-20
|
References |
Application Notes:
This high purity deuterated product is ideal for the identification of sulfatides in samples and biological systems.1 Sulfatide is a type of sulfolipid that is found primarily in the central nervous system and is a myelin-specific sphingolipid. A deficiency of sulfatide in white and gray matter has been associated with Alzheimer’s disease and other types of dementia. Apoliprotein E plays an important regulating role in the metabolism of sulfatides.2 A production of anti-sulfatide antibodies in the cerebrospinal fluid, leading to a deficiency in sulfatides, may be a cause of degeneration of the myelin sheath, leading to multiple sclerosis.3 Metachromatic leukodystrophy is an inherited disorder characterized by a deficiency of the lysosomal enzyme arylsulfatase A and the subsequent accumulation of sulfatide in neural and visceral tissues.4 An immunomodulatory role for sulfatides has been suggested in the pathogenesis of tuberculosis. Sulfatides decrease the in vitro production of proinflammatory cytokines.
References:
1. M. Tan et al. “Biochemical profiling to predict disease severity in metachromatic leukodystrophy” Molecular Genetics and Metabolism, Vol. 99(2) pp. 142-148, 2010
2. H. Cheng, Y. Zhou, D. M. Holtzman, X. Han “Apolipoprotein E mediates sulfatide depletion in animal models of Alzheimer's disease.” Neurobiology of Aging August 2008
3. Ramesh C. Halder, A. Jahng, I. Maricic and Vipin Kumar “Mini Review: Immune Response to Myelin-Derived Sulfatide and CNS-Demyelination” Neurochemical Research, February, Vol. 32(2): 257, 2007
4. Phillip D. Whitfield, Peter C. Sharp, David W. Johnson, Paul Nelson and Peter J. Meikle “Characterization of Urinary Sulfatides in Metachromatic Leukodystrophy Using Electrospray Ionization-Tandem Mass Spectrometry” Molecular Genetics and Metabolism, May Vol. 73(1): 30, 2001
|
Shanghai HuicH Biotech Co., Ltd
Ϻ\(chng)ԁ(li)(zhun)עʳƷzy(c)Ę(bio)(zhn)Ʒ ,(yu)(sh)Ʒϵ:
ˎ: TRC, LGC, USP LKT
ֲ(bio)(zhn)ƷCaroteNature , PhytoLabChromadex,Extrasynthese
(li): Elicityl, TDB, LUDGER Megazyme
֬(li): NU-CHEK Larodan, Avanti Matreya
: ABCAM TCI, ERM, WAKO Jackson Cayman laysan
Ϻ\(chng) ɫa(chn)Ʒ(li)(bio)(zhn)Ʒ֬(bio)(zhn)Ʒؘ(bio)(zhn)Ʒ(li)},ǵʳƷ(bio)(zhn)ƷԃԒ 021-60498804 13917250134 QQ:1715451510
bio-equip.com
Ϻ\(chng)Ƽ˾2010꣬I(y)ּ“|(zh)a(chn)Ʒ\(chng)(w)”\(chng)Գԁ(li)һֱڞ͑ṩһվʽƌW(xu)(w)a(chn)ƷwO(sh)Ӌ(j)_(ki)l(f)ȫ^(gu)ṩ(sh)(yn)O(sh)Ӌ(j)(sh)(yn)ҽO(sh)xO(sh)IJԇg(sh)(w)Ȍ(zhun)(xing)(w)Ϻ\(chng)ﰴտ͑аl(f)a(chn)|(zh)ƭh(hun)(ji)ϸN(yu)|(zh)YԴ(yu)YԴM͑ṩwQ
Ϻ\(chng)Ϻаl(f)ںͽKa(chn)ڏVݺڽӹ˾ϺN(xio)۾W(wng)j(lu)鲼ȫ(gu)͑ṩȫλľCϷ(w)
“ģƵZǰ” Ϻ\(chng){(jng)^(gu)겻иŬĿǰa(chn)ƷƌW(xu)W(xu)ԇ̓xIJ͑鲼t(y)ˎw\ʳƷИI(y)ʯͻԺУоI(lng)
ɫa(chn)Ʒ
ƌW(xu)CrisprϵЮa(chn)ƷMӾA(y)zɹȾ̽ᘣb¹ڿԭwI(y)ø
W(xu)ǻW(xu)о֬(li)ֲۺt(y)ˎԇ
ԇPEGbzwobt(y)ˎoϣͨԇ
xIJģιˇιˇ(x)ίO(jin)y(c)ϵy(tng)
ƷƷ(w)
ƌW(xu)
AbcamAdooQALPCOBiolegendCytivaCaymanDojindoImmunostarInvitrogenJacksonMiltenyiNovoproteinProzymeR&DSinoBiologicalxNStratageneSYSYThermo FisherWakoTopoen
W(xu)
AOCSCarotenatureCILDRElicitylEPGlycarboLarodanMatreyaMegazymeNu-ChekOlchemimPhytolabQCCReageconTLCTRCUSP
ԇ
AladdinAvantiBroadpharmFocusLaysanLKTMacklinSigmaTCIThermo Fishervivitide
xIJģ
xUCorningEppordorf㽭RɡMettler ToledoMilliporeNESTPallRaininWhatmanϺһ