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

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Rabbit polyclonal antibody against human PATE3 protein. Validated for WB and IHC (Paraffin). High purity (>95%) via antigen affinity chromatography. Supplied as liquid in PBS with 50% glycerol. For research use only.

판매단위
pk
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마지막 업데이트 2025. 08. 04. 오전 07:15
Thermo Fisher Scientific PA576081 PATE3 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
731,200원VAT 포함 804,320원

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 Recombinant full length Human PATE3
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage buffer PBS, pH 7.2, with 50% 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_2719808

Product Specific Information

The antibody was affinity-purified from rabbit antiserum using an epitope-specific immunogen. The purity is greater than 95% as determined by SDS-PAGE.


Target Information

PATE3 (prostate and testis expressed protein 3), also known as PATE-DJ or HEL-127, is a 98 amino acid secreted protein containing one UPAR/Ly6 domain and belonging to the PATE family. It is expressed in prostate and testis.
The PATE3 gene spans approximately 3,490 bases and is located on human chromosome 11p15.5. Chromosome 11 contains about 4% of the human genome and is rich in genes associated with various diseases.
Mutations in genes located on chromosome 11 are linked to several disorders, including ataxia-telangiectasia (Atm gene), sickle cell anemia, thalassemia (HBB gene), Wilms’ tumor, WAGR syndrome, Denys-Drash syndrome (WT1 gene), 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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