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Thermo Fisher Scientific PPOX Polyclonal Antibody
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Thermo Fisher Scientific PPOX Polyclonal Antibody

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Thermo Fisher Scientific의 PPOX Polyclonal Antibody는 인간 PPOX 단백질을 인식하는 토끼 유래 다클론 항체입니다. IHC(P) 및 ICC/IF에 적합하며, 항원 친화 크로마토그래피로 정제되었습니다. PBS 기반 완충액에 보관되며 연구용으로 사용됩니다.

카탈로그번호
PA556353
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오전 04:20
Thermo Fisher Scientific PA556353 PPOX Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific PPOX Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human PPOX (Product # RP-94274)
Conjugate Unconjugated
Form Liquid
Concentration 0.2 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, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2645847

Product Specific Information

Immunogen sequence:
ETHLTSRGVS VLRGQPVCGL SLQAEGRWKV SLRDSSLEAD HVISAIPASV LSELLPAEAA PLARALSAIT AVSVAVVNLQ YQGAH

Highest antigen sequence identity to the following orthologs:

  • Mouse: 81%
  • Rat: 76%

Target Information

Protoporphyrinogen oxidase (PPOX) is the penultimate enzyme in the heme biosynthetic pathway, catalyzing the 6-electron oxidation of protoporphyrinogen IX to form protoporphyrin IX. The PPOX protein localizes to the inner mitochondrial membrane in various tissues including heart, brain, placenta, lung, liver, skeletal muscle, kidney, and pancreas. Genetic deficiency of PPOX results in variegate porphyria, an autosomal dominant disorder characterized by cutaneous photosensitivity and/or neurological manifestations. The rare homozygous variant causes severe PPOX deficiency, leading to early-onset photosensitization, skeletal abnormalities of the hand, short stature, mental retardation, and convulsions.


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

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