×
我们推荐在您的浏览器上开启Javascript,以获得最佳效果。
HSD17B4 抗体 (AA 18-231)
HSD17B4
适用: 人
WB, IHC
宿主: 兔
Polyclonal
unconjugated
HSD17B4抗体详情
(hide)
抗原
See all HSD17B4 抗体
HSD17B4
(Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4))
抗原表位
All epitopes for HSD17B4 抗体
AA 18-231
适用
All reactivities for HSD17B4 抗体
人
宿主
All hosts for HSD17B4 抗体
兔
克隆类型
All clonalities for HSD17B4 抗体
多克隆
标记
All conjugates for HSD17B4 抗体
This HSD17B4 antibody is un-conjugated
应用范围
All applications for HSD17B4 抗体
Western Blotting (WB), Immunohistochemistry (IHC)
纯化方法
Purified by antigen-affinity chromatography.
免疫原
Recombinant protein fragment contain a sequence corresponding to a region within amino acids 18 and 231 of MFE-2
Top Product
Discover our top product HSD17B4 Primary Antibody
Alternatives
(show)
使用细节
(hide)
应用备注
Suggested dilutions: Western blotting: 1.500-1.3000 Immunohistochemistry: 1.100-1.500
限制
仅限研究用
贮存及处理
(hide)
状态
Liquid
缓冲液
0.1 M Tris-buffered saline with 20 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
储存液
Thimerosal (Merthiolate)
注意事项
Biohazard Informations: This product contains thimerosal which is hazardous.
储存条件
4 °C/-20 °C
储存方法
Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
HSD17B4目标详情
(hide)
抗原
HSD17B4
(Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4))
别名
MFE-2 (HSD17B4 产品 )
别名
zgc:55545 antibody, zgc:77300 antibody, CG3415 antibody, DmMFE-2 antibody, Dmel\\CG3415 antibody, MFE-2 antibody, DBP antibody, MPF-2 antibody, PRLTS1 antibody, SDR8C1 antibody, 17-beta-HSD antibody, 17[b]-HSD antibody, 4 antibody, MFP2 antibody, Mfp-2 antibody, perMFE-2 antibody, hydroxysteroid (17-beta) dehydrogenase 4 antibody, hydroxysteroid 17-beta dehydrogenase 4 antibody, peroxisomal Multifunctional enzyme type 2 antibody, hsd17b4 antibody, HSD17B4 antibody, Mfe2 antibody, Hsd17b4 antibody
背景
The protein encoded by this gene is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids.It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids.Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD).An apparent pseudogene of this gene is present on chromosome 8.[provided by RefSeq]
分子量
80 kDa
基因ID
3295
途径
Monocarboxylic Acid Catabolic Process
Recently viewed
(hide)