SCP2 Protein (Transcript Variant 4) (Myc-DYKDDDDK Tag)

Catalog No. ABIN2731506

This Recombinant SCP2 protein is produced in HEK-293 Cells.

Quick Overview for SCP2 Protein (Transcript Variant 4) (Myc-DYKDDDDK Tag) (ABIN2731506)

Target: SCP2 (Sterol Carrier Protein 2 (SCP2))

Protein Type: Recombinant

Origin: Human

Source: HEK-293 Cells

Application: Antibody Production (AbP), Standard (STD)

Purity: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Product Details

Protein Characteristics: Transcript Variant 4

Purification tag / Conjugate: This SCP2 protein is labelled with Myc-DYKDDDDK Tag.

Characteristics:

• Recombinant human SCP2 / SCPX (transcript variant 4) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Application Details

Application Notes: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Comment:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Handling

Concentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Storage: -80 °C

Storage Comment: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Target Details

Target: SCP2 (Sterol Carrier Protein 2 (SCP2))

Alternative Name: Scp2,scpx

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.[provided by RefSeq, Aug 2010].

Molecular Weight: 13.2 kDa

NCBI Accession: NP_001007101

Pathways: C21-Steroid Hormone Metabolic Process, Monocarboxylic Acid Catabolic Process