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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 Thermo Fisher Scientific의 토끼 폴리클로날 항체. Western blot, IHC, IP 등 다양한 응용에 적합하며, 항원 친화 크로마토그래피로 정제됨. 인간 및 생쥐 시료 반응성. 4°C에서 보관.

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마지막 업데이트 2025. 08. 03. 오후 02:26
Thermo Fisher Scientific A301580A CPSF160 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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658,900원VAT 포함 724,790원

Thermo Fisher Scientific · Thermo Fisher Scientific CPSF160 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution / Amount
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
Species Reactivity Human, Mouse
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
Purification Antigen affinity chromatography
Storage Buffer TBS, pH 7.0–8.0, with 0.1% BSA
Contains 0.09% sodium azide
Storage Conditions 4°C
Shipping Conditions Wet ice

Product Specific Information

  • Recommended shelf life: 1 year from date of receipt
  • 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
  • One RING-type zinc finger

Midline-1 is believed to have E3 ubiquitin ligase activity, targeting the catalytic subunit of protein phosphatase 2 for degradation.
It is a cytoplasmic protein found as a homodimer or heterodimer 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 (e.g., hypospadias in males, splayed labia in females)
  • Lip-palate-laryngotracheal clefts
  • Imperforate anus
  • Developmental delay
  • Congenital heart defects

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

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