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SCP2 Polyclonal Antibody

规格: / 20μL / 60μL / 120μL / 200μL
价格: / ¥420 / ¥1010 / ¥1640 / ¥2365

货号:E-AB-52211

宿主: Rabbit

反应性: H,M,R

应用: WB,IHC

  • 详情
  • Overview

    Synonyms DKFZp686C12188,DKFZp686D11188,NLTP,NLTP,Non-specific lipid-transfer protein,Nonspecific lipid transfer protein,NSL TP,NSL-TP,OTTHUMP00000010488,OTTHUMP00000231766,OTTHUMP00000231767,OTTHUMP00000231768,OTTHUMP00000231769,OTTHUMP00000231770,OTTHUMP00000231772,OTTHUMP00000231773,OTTHUMP00000231774,OTTHUMP00000231776,OTTHUMP00000234662,Propanoyl CoA C acyltransferase,Propanoyl-CoA C-acyltransferase,SCP 2,SCP chi ,SCP X,SCP-2,SCP-chi,SCP-X,SCP2,SCPchi ,SCPX,Sterol carrier protein 2,Sterol carrier protein X,SCP2抗体
    Swissprot P22307
    Source Rabbit
    Reactivity Human,Mouse,Rat
    Immunogen Fusion protein of human SCP2
    Application WB(Detection kit: E-IR-R304),IHC(Detection kit: E-IR-R213)
    Recommended dilution WB,,1:500-1:2000;IHC,,1:25-1:100;
    Concentration 0.6mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Mitochondrion; Cytoplasm. Mitochondrion. Cytoplasmic in the liver and also associated with mitochondria especially in steroidogenic tissues and Peroxisome. Interaction with PEX5 is essential for peroxisomal import.
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.05% NaN3 and 40% Glycerol,pH7.4
    Background This gene encodes two proteins: sterol carrier protein X (SCPx) and sterol carrier protein 2 (SCP2), as a result of transcription initiation from 2 independently regulated promoters. The transcript initiated from the proximal promoter encodes the longer SCPx protein, and the transcript initiated from the distal promoter encodes the shorter SCP2 protein, with the 2 proteins sharing a common C-terminus. Evidence suggests that the SCPx protein is a peroxisome-associated thiolase that is involved in the oxidation of branched chain fatty acids, while the SCP2 protein is thought to be an intracellular lipid transfer protein. This gene is highly expressed in organs involved in lipid metabolism, and may play a role in Zellweger syndrome, in which cells are deficient in peroxisomes and have impaired bile acid synthesis. Alternative splicing of this gene produces multiple transcript variants, some encoding different isoforms.
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