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Thermo Fisher Scientific CPSF160 Polyclonal Antibody
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Thermo Fisher Scientific CPSF160 Polyclonal Antibody

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CPSF160 단백질을 인식하는 Rabbit Polyclonal 항체로 Western blot, IHC, IP에 적합합니다. 4°C에서 보관하며, 1년의 권장 유효기간을 가집니다. 인간 CPSF1 단백질의 1392-1442번 잔기 영역을 면역원으로 사용했습니다.

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마지막 업데이트 2025. 08. 03. 오후 02:28
Thermo Fisher Scientific A301580AM CPSF160 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
477,300원VAT 포함 525,030원
Thermo Fisher Scientific A301580AT CPSF160 Polyclonal Antibody 10 ul pk판매 단위 pk ·
재고 확인 필요
194,600원VAT 포함 214,060원

Thermo Fisher Scientific · Thermo Fisher Scientific CPSF160 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:2,000–1:10,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:100–1:500
Immunoprecipitation (IP) 2–10 µg/mg lysate

Product Specifications

항목 내용
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Region between residue 1392 and 1442 of human cleavage and polyadenylation specific factor 1, 160kD subunit
Conjugate Unconjugated
Form Liquid
Concentration 0.20 mg/mL
Storage conditions 4°C
Shipping conditions Wet ice

Product Specific Information

  • Recommended shelf life: 1 year from date of receipt
  • Application Note: For IHC, epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.
  • Based on 100% sequence identity, this antibody is predicted to react with Bovine.

Target Information

Midline-1 (Tripartite motif-containing protein 18, Putative transcription factor XPRF, RING finger protein 59) is a 667 amino acid protein encoded by the human gene MID1.
Midline-1 belongs to the TRIM/RBCC family and contains two B box-type zinc fingers, one B30.2/SPRY domain, one COS domain, one fibronectin type-III domain, and one RING-type zinc finger.
It is believed to have E3 ubiquitin ligase activity that targets the catalytic subunit of protein phosphatase 2 for degradation.
This cytoplasmic protein can form homodimers or heterodimers with Midline-2 and interacts with IGBP1 (Lymphocyte signaling protein A4).
Defects in MID1 cause Opitz syndrome type I (OS-I), an X-linked recessive disorder characterized by hypertelorism, genital-urinary defects, cleft lip/palate, imperforate anus, developmental delay, and congenital heart defects.


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

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