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Thermo Fisher Scientific SCP2 Polyclonal Antibody
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Thermo Fisher Scientific SCP2 Polyclonal Antibody

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Human SCP2 단백질을 인식하는 Rabbit Polyclonal Antibody로 WB, IHC(P), ICC/IF에 적합. 항원 친화 크로마토그래피로 정제되어 높은 특이성과 재현성을 제공. PBS 기반 용액 형태로 장기 보관 시 -20°C에서 안정적 유지.

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pk
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마지막 업데이트 2025. 08. 04. 오후 01:54
Thermo Fisher Scientific PA555580 SCP2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific SCP2 Polyclonal Antibody

Applications

Application Tested Dilution Publications
Western Blot (WB) 0.04–0.4 µg/mL -
Immunohistochemistry (Paraffin) (IHC (P)) 1:200–1:500 -
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL -

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human SCP2. Recombinant protein control fragment (Product #RP-94063).
Conjugate Unconjugated
Form Liquid
Concentration 0.1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% glycerol
Contains 0.02% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2647026

Product Specific Information

Immunogen sequence:
IKMVGFDMSK EAARKCYEKS GLTPNDIDVI ELHDCFSTNE LLTYEALGLC PEGQGATLVD RGDNTYGGKW VINPSGGLIS KG

Highest antigen sequence identity to the following orthologs:

  • Mouse: 91%
  • Rat: 93%

Target Information

This gene encodes two proteins: sterol carrier protein X (SCPx) and sterol carrier protein 2 (SCP2), resulting from transcription initiation from two independently regulated promoters.

  • The proximal promoter encodes the longer SCPx protein.
  • The distal promoter encodes the shorter SCP2 protein, sharing a common C-terminus.

SCPx is a peroxisome-associated thiolase involved in oxidation of branched-chain fatty acids, while SCP2 functions as an intracellular lipid transfer protein.
This gene is highly expressed in organs related to lipid metabolism and may be implicated in Zellweger syndrome, characterized by peroxisome deficiency and impaired bile acid synthesis.
Alternative splicing generates multiple transcript variants encoding different isoforms.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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