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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 및 생쥐 시료에서 PPOX 단백질 검출에 적합한 토끼 폴리클로날 항체입니다. Western blot, IHC, ELISA 등 다양한 응용에 사용 가능하며, 고순도 친화 크로마토그래피 정제 및 안정한 PBS/glycerol 보존액 형태로 제공됩니다.

카탈로그번호
PA5117044
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 08:33
Thermo Fisher Scientific PA5117044 PPOX Polyclonal Antibody 100 ul pk판매 단위 pk ·
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655,000원VAT 포함 720,500원

Thermo Fisher Scientific · Thermo Fisher Scientific PPOX Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
ELISA 1 µg/mL

Product Specifications

항목 내용
Species Reactivity Mouse, Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fusion protein containing a sequence corresponding to amino acids 1–280 of human PPOX (NP_001116236.1)
Conjugate Unconjugated
Form Liquid
Concentration 0.47 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions –20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2901674

Product Specific Information

  • Positive Samples: HepG2, Mouse spleen, Mouse liver, Mouse kidney
  • Immunogen sequence:
    MGRTVVVLGG GISGLAASYH LSRAPCPPKV VLVESSERLG GWIRSVRGPN GAIFELGPRG IRPAGALGAR TLLLVSELGL DSEVLPVRGD HPAAQNRFLY VGGALHALPT GLRGLLRPSP PFSKPLFWAG LRELTKPRGK EPDETVHSFA QRRLGPEVAS LAMDSLCRGV FAGNSRELSI RSCFPSLFQA EQTHRSILLG LLLGAGRTPQ PDSALIRQAL AERWSQWSLR GGLEMLPQAL ETHLTSRGVS VLRGQPVCGL SLQAEGRWKV SLRDSSLEAD

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. PPOX is localized to the inner mitochondrial membrane in tissues such as heart, brain, placenta, lung, liver, skeletal muscle, kidney, and pancreas.
Genetic deficiency of PPOX results in variegate porphyria (VP), an autosomal dominant disorder characterized by cutaneous photosensitivity and neurological manifestations. The rare homozygous variant of VP leads to severe PPOX deficiency, early-onset photosensitization, skeletal abnormalities, 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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