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

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MID1 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody로, WB, ICC/IF, ELISA에 적합합니다. 인간 및 생쥐 반응성을 가지며, 고순도 친화 크로마토그래피 정제 제품입니다. 연구용으로만 사용됩니다.

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마지막 업데이트 2025. 08. 04. 오전 03:48
Thermo Fisher Scientific PA5109957 MID1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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627,600원VAT 포함 690,360원

Thermo Fisher Scientific · Thermo Fisher Scientific MID1 Polyclonal Antibody

Thermo Fisher Scientific MID1 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunocytochemistry (ICC/IF) 1:50–1:100
ELISA 1 µg/mL

Product Specifications

Specification Description
Species Reactivity Human, Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fusion protein containing amino acids 478–667 of human MID1 (NP_000372.1)
Conjugate Unconjugated
Form Liquid
Concentration 0.54 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2855368

Product Specific Information

Immunogen sequence:
KLKTNSQPFK LDPKSAHRKL KVSHDNLTVE RDESSSKKSH TPERFTSQGS YGVAGNVFID SGRHYWEVVI SGSTWYAIGL AYKSAPKHEW IGKNSASWAL CRCNNNWVVR HNSKEIPIEP APHLRRVGIL LDYDNGSIAF YDALNSIHLY TFDVAFAQPV CPTFTVWNKC LTIITGLPIP DHLDCTEQLP

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, lip-palate-laryngotracheal clefts, 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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