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Thermo Fisher Scientific CPSF1 Polyclonal Antibody
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Thermo Fisher Scientific CPSF1 Polyclonal Antibody

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CPSF1 단백질을 인식하는 Rabbit Polyclonal 항체로, Human 및 Mouse 시료에 반응합니다. Western blot과 ELISA에 적합하며, 고순도의 Affinity chromatography로 정제되었습니다. PBS/glycerol buffer에 보존되며 연구용으로 사용됩니다.

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마지막 업데이트 2025. 08. 05. 오전 03:30
Thermo Fisher Scientific PA5116722 CPSF1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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655,000원VAT 포함 720,500원

Thermo Fisher Scientific · Thermo Fisher Scientific CPSF1 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
ELISA 1 µg/mL

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fusion protein containing amino acids 700–950 of human CPSF1 (NP_0374232)
Conjugate Unconjugated
Form Liquid
Concentration 1.65 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol
Contains 0.01% thimerosal
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2901353

Product Specific Information

  • Positive Samples: 293T, NIH/3T3, Mouse liver
  • Immunogen sequence:
    LYRDLSGMFT TESRLGGARD ELGGRSGPEA EGLGSETSPT VDDEEEMLYG DSGSLFSPSK EEARRSSQPP ADRDPAPFRA EPTHWCLLVR ENGTMEIYQL PDWRLVFLVK NFPVGQRVLV DSSFGQPTTQ GEARREEATR QGELPLVKEV LLVALGSRQS RPYLLVHVDQ ELLIYEAFPH DSQLGQGNLK VRFKKVPHNI NFREKKPKPS KKKAEGGGAE EGAGARGRVA RFRYFEDIYG YSGVFICGPS P

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 exhibits E3 ubiquitin ligase activity, targeting the catalytic subunit of protein phosphatase 2 for degradation. It forms homo- 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.

Safety Information

WARNING: This product can expose you to chemicals including mercury, known to the State of California to cause birth defects or other reproductive harm.
For more information, visit www.P65Warnings.ca.gov.

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

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