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Thermo Fisher Scientific PATE3 Polyclonal Antibody
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Thermo Fisher Scientific PATE3 Polyclonal Antibody

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PATE3 단백질을 인식하는 Rabbit Polyclonal 항체로, Western blot과 IHC(Paraffin)에서 검증됨. Human, Mouse, Rat 시료에 반응하며, Affinity chromatography로 정제된 액상 형태. PBS 및 50% glycerol buffer에 보관, -20°C에서 저장.

카탈로그번호
PA5102606
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 10:28
Thermo Fisher Scientific PA5102606 PATE3 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
764,500원VAT 포함 840,950원

Thermo Fisher Scientific · Thermo Fisher Scientific PATE3 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 1:500–1:2,000

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1:50–1:200

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen A synthesized peptide derived from human PATE3 (Accession B3GLJ2), corresponding to amino acid residues Y12–Q62
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C
Shipping Conditions Wet ice
RRID AB_2815924

Product Specific Information

Antibody detects endogenous levels of total PATE3.


Target Information

PATE3 (prostate and testis expressed protein 3), also known as PATE-DJ or HEL-127, is a 98 amino acid protein containing one UPAR/Ly6 domain and belongs to the PATE family. PATE3 is a secreted protein expressed in the prostate and testis. The gene encoding PATE3 spans approximately 3,490 bases and maps to human chromosome 11p15.5.

Chromosome 11 comprises about 4% of the human genome and is rich in genes associated with various diseases. The ATM gene on chromosome 11 regulates cell cycle arrest and apoptosis following DNA double-strand breaks, and its mutation causes ataxia-telangiectasia. Other notable disorders linked to chromosome 11 include sickle cell anemia, thalassemia, Wilms’ tumor, WAGR syndrome, Denys-Drash syndrome, Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema, and Smith-Lemli-Opitz syndrome.


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

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