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当前位置: 首页 > 产品中心 > Recombinant_antibodies > Prosci/ABHD5抗体/29-752/100微克
商品详细Prosci/ABHD5抗体/29-752/100微克
Prosci/ABHD5抗体/29-752/100微克
Prosci/ABHD5抗体/29-752/100微克
商品编号: 29-752
品牌: prosci-inc
市场价: ¥6500.00
美元价: 3900.00
产地: 美国(厂家直采)
公司:
产品分类: 重组抗体
公司分类: Recombinant_antibodies
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

Specifications

SPECIES REACTIVITY:Human, Mouse, Rat
TESTED APPLICATIONS:ELISA, WB
APPLICATIONS:ABHD5 antibody can be used for detection of ABHD5 by ELISA at 1:312500. ABHD5 antibody can be used for detection of ABHD5 by western blot at 5.0 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
USER NOTE:Optimal dilutions for each application to be determined by the researcher.
POSITIVE CONTROL:1) Tranfected 293T Cell Lysate
PREDICTED MOLECULAR WEIGHT:39 kDa
IMMUNOGEN:Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ABHD5.
HOST SPECIES:Rabbit

Properties

PURIFICATION:Antibody is purified by protein A chromatography method.
PHYSICAL STATE:Lyophilized
BUFFER:Antibody is lyophilized in PBS buffer with 2% sucrose. Add 100 μL of distilled water. Final antibody concentration is 1 mg/mL.
CONCENTRATION:1 mg/ml
STORAGE CONDITIONS:For short periods of storage (days) store at 4˚C. For longer periods of storage, store ABHD5 antibody at -20˚C. As with any antibody avoid repeat freeze-thaw cycles.
CLONALITY:Polyclonal
CONJUGATE:Unconjugated

Additional Info

ALTERNATE NAMES:ABHD5, CDS, CGI58, IECN2, MGC8731, NCIE2
ACCESSION NO.:NP_057090
PROTEIN GI NO.:31542303
OFFICIAL SYMBOL:ABHD5
GENE ID:51099

Background

BACKGROUND:ABHD5 belongs to a large family of proteins defined by an alpha/beta hydrolase fold, and contains three sequence motifs that correspond to a catalytic triad found in the esterase/lipase/thioesterase subfamily. It differs from other members of this subfamily in that its putative catalytic triad contains an asparagine instead of the serine residue. Mutations in ABHD5 gene have been associated with Chanarin-Dorfman syndrome, a triglyceride storage disease with impaired long-chain fatty acid oxidation.The protein encoded by this gene belongs to a large family of proteins defined by an alpha/beta hydrolase fold, and contains three sequence motifs that correspond to a catalytic triad found in the esterase/lipase/thioesterase subfamily. It differs from other members of this subfamily in that its putative catalytic triad contains an asparagine instead of the serine residue. Mutations in this gene have been associated with Chanarin-Dorfman syndrome, a triglyceride storage disease with impaired long-chain fatty acid oxidation.
REFERENCES: 1) Bruno, C., (2008) Biochem. Biophys. Res. Commun. 369 (4), 1125-1128.
品牌介绍
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