
IHC-P analysis of human liver- using GTX88705 SCP2 antibody, Internal. Antigen retrieval : citrate buffer pH 6 Dilution : 3.8microg/ml
SCP2 antibody, Internal
GTX88705
ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetSCP2
Overview
- SupplierGeneTex
- Product NameSCP2 antibody, Internal
- Delivery Days Customer7
- Antibody SpecificityThis antibody is expected to recognize isoform 1, 2, 6, 7 and 8 (NP_002970.2; NP_001007099.1; NP_001180529.1; NP_001180528.1; NP_001180546.1 respectively)
- Application Supplier NoteIHC-P: 3-6microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
- ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
- CertificationResearch Use Only
- ClonalityPolyclonal
- Concentration0.50 mg/ml
- ConjugateUnconjugated
- Gene ID6342
- Target nameSCP2
- Target descriptionsterol carrier protein 2
- Target synonymsacetyl-CoA C-myristoyltransferase; epididymis secretory sperm binding protein; NLTP; non-specific lipid-transfer protein; NSL-TP; propanoyl-CoA C-acyltransferase; SCOX; SCP-2; SCP-2/3-oxoacyl-CoA thiolase; SCP-2/thiolase; SCP-CHI; SCPX; SCP-X; sterol carrier protein 2; sterol carrier protein X; straight-chain acyl-CoA oxidase
- HostGoat
- IsotypeIgG
- Protein IDP22307
- Protein NameNon-specific lipid-transfer protein
- Scientific DescriptionThis 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.[provided by RefSeq, Aug 2010]
- ReactivityHuman
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203