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Thermo Fisher Scientific MID1 Polyclonal Antibody
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Thermo Fisher Scientific MID1 Polyclonal Antibody

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Human MID1 단백질을 표적으로 하는 Rabbit Polyclonal Antibody로 Western blot 및 Immunoprecipitation에 사용 가능. 항원 친화 크로마토그래피로 정제되었으며 액상 형태, 1 mg/mL 농도. 4°C 보관, 연구용 전용.

카탈로그번호
A302227Ax (2개 옵션)
판매단위
pk
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2개 옵션
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마지막 업데이트 2025. 08. 05. 오전 02:38
Thermo Fisher Scientific A302227A MID1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
658,900원VAT 포함 724,790원
Thermo Fisher Scientific A302227AT MID1 Polyclonal Antibody 10 ul pk판매 단위 pk ·
재고 확인 필요
194,600원VAT 포함 214,060원

Thermo Fisher Scientific · Thermo Fisher Scientific MID1 Polyclonal Antibody

Applications

Application Tested Dilution
Western Blot (WB) 1:2,000–1:10,000
Immunoprecipitation (IP) Assay-dependent

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Region between residue 617 and 667 of human midline 1
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer Tris citrate/phosphate, pH 7–8
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
  • Based on 100% sequence identity, predicted to react with Rat

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.
It 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 that forms 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 (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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