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Anti-Acid sphingomyelinase/SMPD1 Polyclonal Antibody

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Anti-Acid sphingomyelinase/SMPD1 Polyclonal Antibody
产品编号 TMAB-00037

Anti-Acid sphingomyelinase/SMPD1 Polyclonal Antibody 是一种 Rabbit 抗体,靶向 Acid sphingomyelinase/SMPD1。Anti-Acid sphingomyelinase/SMPD1 Polyclonal Antibody 可用于 WB,IHC-P,IHC-Fr,IF,FCM。

Anti-Acid sphingomyelinase/SMPD1 Polyclonal Antibody

Anti-Acid sphingomyelinase/SMPD1 Polyclonal Antibody

Rating icon 还可以
Anti-Acid sphingomyelinase/SMPD1 Polyclonal Antibody
产品编号 TMAB-00037

Anti-Acid sphingomyelinase/SMPD1 Polyclonal Antibody 是一种 Rabbit 抗体,靶向 Acid sphingomyelinase/SMPD1。Anti-Acid sphingomyelinase/SMPD1 Polyclonal Antibody 可用于 WB,IHC-P,IHC-Fr,IF,FCM。

规格价格库存数量
50 μL
¥ 1,165
5日内发货
100 μL
¥ 1,970
5日内发货
200 μL
¥ 2,795
5日内发货
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产品介绍

生物活性
产品描述
Anti-Acid sphingomyelinase/SMPD1 Polyclonal Antibody is a Rabbit antibody targeting Acid sphingomyelinase/SMPD1. Anti-Acid sphingomyelinase/SMPD1 Polyclonal Antibody can be used in WB,IHC-P,IHC-Fr,IF,FCM.
Ig Type
IgG
交叉反应
Human,Mouse,Rat (predicted:Dog,Pig,Cow,Rabbit)
验证活性
1. Paraformaldehyde-fixed, paraffin embedded (Rat brain); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 min; Blocking buffer (normal goat serum) at 37°C for 30 min; Antibody incubation with (Acid sphingomyelinase) Polyclonal Antibody, Unconjugated (TMAB-00037) at 1:400 overnight at 4°C, followed by operating according to SP Kit (Rabbit) instructionsand DAB staining.
2. Sample:
HepG2 (human) cell Lysate at 30 μg
MCF-7 (human) cell Lysate at 30 μg
A431 (human) cell Lysate at 30 μg
Hale (human) cell Lysate at 30 μg
Primary: Anti-Acid sphingomyelinase (TMAB-00037) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 64 kDa
Observed band size: 69 kDa
3. Blank control: A431. Primary Antibody (green line): Rabbit Anti-Acid sphingomyelinase antibody (TMAB-00037)
Dilution: 2 μg/10^6 cells;
Isotype Control Antibody (orange line): Rabbit IgG.
Secondary Antibody: Goat anti-rabbit IgG-PE
Dilution: 1 μg/test.
Protocol
The cells were fixed with 4% PFA (10 min at room temperature) and then permeabilized with 0.1% PBST for 20 min at room temperature. The cells were then incubated in 5% BSA to block non-specific protein-protein interactions for 30 min at room temperature. Cells stained with Primary Antibody for 30 min at room temperature. The secondary antibody used for 40 min at room temperature.
应用
推荐剂量
WB: 1:500-2000; IHC-P: 1:100-500; IHC-Fr: 1:100-500; IF: 1:100-500; FCM: 2ug/Test
抗体种类
Polyclonal
宿主来源Rabbit
亚细胞定位Lysosome.
构建方式Hybridoma Polyclonal Antibody
纯化方式Protein A purified
性状Liquid
缓冲液0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
研究背景Converts sphingomyelin to ceramide. Also has phospholipase C activities toward 1,2-diacylglycerolphosphocholine and 1,2-diacylglycerolphosphoglycerol. Isoform 2 and isoform 3 have lost catalytic activity. Involvement in disease: Defects in SMPD1 are the cause of Niemann-Pick disease type A (NPDA) ; also known as Niemann-Pick disease classical infantile form. It is an early-onset lysosomal storage disorder caused by failure to hydrolyze sphingomyelin to ceramide. It results in the accumulation of sphingomyelin and other metabolically related lipids in reticuloendothelial and other cell types throughout the body, leading to cell death. Niemann-Pick disease type A is a primarily neurodegenerative disorder characterized by onset within the first year of life, mental retardation, digestive disorders, failure to thrive, major hepatosplenomegaly, and severe neurologic symptoms. The severe neurological disorders and pulmonary infections lead to an early death, often around the age of four. Clinical features are variable. A phenotypic continuum exists between type A (basic neurovisceral) and type B (purely visceral) forms of Niemann-Pick disease, and the intermediate types encompass a cluster of variants combining clinical features of both types A and B.
抗原信息
免疫原
KLH conjugated synthetic peptide: human Acid sphingomyelinase
抗原种属
Human
基因ID
Uniprot ID
研究领域
Associated Proteins,Neurodegenerative disease,Lipid metabolism
存储&运输
储存方式Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles.
运输方式Shipping with blue ice.

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