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SCP2 Polyclonal Antibody Reactivity Mouse

SKU: E-AB-52211-200

  • $ 55995
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SCP2 Polyclonal Antibody Reactivity Mouse

 

SKU # E-AB-52211
Reactivity Human, Mouse, Rat
Host Rabbit
Applications WB, IHC

 

Product Details

Isotype IgG
Host Rabbit
Reactivity Human, Mouse, Rat
Applications WB, IHC
Clonality Polyclonal
Immunogen Fusion protein of human SCP2
Abbre SCP2
Synonyms DKFZp686C12188,  DKFZp686D11188,  NLTP,  NSL TP,  NSL-TP,  Non-specific lipid-transfer protein,  Nonspecific lipid transfer protein,  OTTHUMP00000010488,  OTTHUMP000002317,  OTTHUMP00000231766,  OTTHUMP00000231767,  OTTHUMP00000231768,  OTTHUMP00000231769,  OTTHUMP00000231770
Swissprot
Calculated MW 59 kDa
Observed MW Refer to figures
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.
Concentration 0.6 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Purification Method Antigen affinity purification
Research Areas Cancer,  Metabolism,  Signal transduction
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack, upon receipt, store it immediately at the temperature recommended.

 

Related Reagents

Applications Recommended Dilution
WB 1:500-1:2000
IHC 1:25-1:100

 

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.