PIMA526336

SCP2 Monoclonal Antibody (OTI1D2), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIMA526336-Each-of-1 In Stock ₹ 52,198.50

PIMA526336 - Each of 1

₹ 52,198.50

In Stock

Quantity

1

Base Price: ₹ 52,198.50

GST (18%): ₹ 9,395.73

Total Price: ₹ 61,594.23

Antigen

SCP2

Classification

Monoclonal

Concentration

1 mg/mL

Formulation

PBS with 1% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3

Gene Accession No.

P22307

Gene Symbols

SCP2

Immunogen

Full length human recombinant protein of SCP2 produced in HEK293T cell

Quantity

100μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG1

Applications

Immunohistochemistry (Paraffin), Western Blot

Clone

OTI1D2

Conjugate

Unconjugated

Gene

SCP2

Gene Alias

AA409774; AA409893; C76618; C79031; NLTP; nonspecific lipid transfer protein; Non-specific lipid-transfer protein; NSLIPTR; ns-LTP; NSL-TP; propanoyl-CoA C-acyltransferase; SCP2; SCP-2; SCP-CHI; SCPX; SCP-X; Sterol carrier protein 2; sterol carrier protein 2, liver; sterol carrier protein X

Host Species

Mouse

Purification Method

Affinity Chromatography

Regulatory Status

RUO

Gene ID (Entrez)

6342

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

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Description

  • 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.