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

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Thermo Fisher Scientific의 MID1 Polyclonal Antibody는 인간, 마우스, 랫트 시료에서 MID1 단백질을 검출하는 토끼 유래 IgG 항체입니다. Western blot, IHC, IP에 사용 가능하며, 고순도(>95%) 항원 친화 크로마토그래피 정제 제품입니다. 연구용으로만 사용됩니다.

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마지막 업데이트 2025. 08. 04. 오후 11:02
Thermo Fisher Scientific PA536305 MID1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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630,500원VAT 포함 693,550원

Thermo Fisher Scientific · Thermo Fisher Scientific MID1 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1:500–1:1,000 -
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200 -
Immunoprecipitation (IP) - 1 publication

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Published Species Not Applicable
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to amino acids 71–120 of human Midline-1
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_2553463

Product Specific Information

  • Detects endogenous protein at approximately 75 kDa.
  • Purity >95% by SDS-PAGE.

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 functions as an E3 ubiquitin ligase, targeting the catalytic subunit of protein phosphatase 2 for degradation.
It is a cytoplasmic protein forming 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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