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Thermo Fisher Scientific PRPF18 Polyclonal Antibody
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Thermo Fisher Scientific PRPF18 Polyclonal Antibody

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PRPF18 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody. Western blot 및 IHC(P)에서 사용 가능. 인간, 마우스, 랫트 반응성. 항원 친화 크로마토그래피로 정제된 액상 항체로, 장기 보관 시 -20°C에서 보관.

카탈로그번호
PA558031
판매단위
pk
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마지막 업데이트 2025. 08. 01. 오후 07:05
Thermo Fisher Scientific PA558031 PRPF18 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific PRPF18 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 0.04–0.4 µg/mL

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1:200–1:500

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human PRPF18. Recombinant protein control fragment (Product #RP-97130)
Conjugate Unconjugated
Form Liquid
Concentration 0.3 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 storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2645968

Product Specific Information

  • Immunogen sequence:
    SNPVLELELA EEKLPMTLSR QEVIRRLRER GEPIRLFGET DYDAFQRLRK IEILTPEVNK GLRNDLKAAL DKIDQQYLNE IVG
  • Highest antigen sequence identity to the following orthologs:
    Mouse – 100%, Rat – 99%.

Target Information

PRPF18 (pre-mRNA-splicing factor 18), also known as HPRP18, is a 342 amino acid protein that localizes to nuclear speckles and plays a role in the second step of pre-mRNA splicing. A member of the PRP18 family, PRPF18 contains seven WD repeats and exists as two alternatively spliced isoforms encoded by a gene located on human chromosome 10p13.

Chromosome 10 contains over 800 genes and 135 million nucleotides. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. Other chromosome 10 associated disorders include Cockayne syndrome, tetrahydrobiopterin deficiency, and trisomy 10.


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

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