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Thermo Fisher Scientific ENPP4 Polyclonal Antibody
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Thermo Fisher Scientific ENPP4 Polyclonal Antibody

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Thermo Fisher Scientific의 ENPP4 Polyclonal Antibody는 인간 ENPP4 단백질을 검출하는 토끼 IgG 기반 항체입니다. Western blot과 IHC(P) 실험에 적합하며, 항원 친화 크로마토그래피로 정제되었습니다. 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 05. 오후 12:00
Thermo Fisher Scientific PA550655 ENPP4 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
630,500원VAT 포함 693,550원

Thermo Fisher Scientific · Thermo Fisher Scientific ENPP4 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 1:500–1:2,000

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1:25–1:100

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to a region derived from internal residues of human ectonucleotide pyrophosphatase/phosphodiesterase 4 (putative)
Conjugate Unconjugated
Form Liquid
Concentration 1.5 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.4, with 40% glycerol
Contains 0.05% sodium azide
Storage Conditions -20°C
Shipping Conditions Wet ice
RRID AB_2636107

Product Specific Information

The antibody detects endogenous levels of total ENPP4 protein.

Target Information

NPP4, also known as ENPP4 (ectonucleotide pyrophosphatase/phosphodiesterase family member 4), is a 453 amino acid single-pass type I membrane protein belonging to the nucleotide pyrophosphatase/phosphodiesterase family.
The gene encoding NPP4 spans approximately 16,736 bases and maps to human chromosome 6p21.1. Chromosome 6 comprises about 6% of the human genome, containing roughly 1,200 genes within 170 million base pairs.
Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer, suggesting a cancer susceptibility locus. Porphyria cutanea tarda is linked to chromosome 6 through the HFE gene, and Stickler syndrome, 21-hydroxylase deficiency, and maple syrup urine disease are also associated with genes on this chromosome.
Notably, the PARK2 gene (related to Parkinson’s disease) and genes encoding major histocompatibility complex proteins are located on chromosome 6. A bipolar disorder susceptibility locus has also been identified on the q arm of chromosome 6.


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

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