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

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Rabbit polyclonal antibody against human CPSF1. Validated for ICC/IF applications. Antigen affinity purified and supplied in PBS with 40% glycerol. Suitable for research use only. High sequence identity with mouse and rat orthologs.

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마지막 업데이트 2025. 08. 04. 오후 10:05
Thermo Fisher Scientific PA567022 CPSF1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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791,800원VAT 포함 870,980원

Thermo Fisher Scientific · Thermo Fisher Scientific CPSF1 Polyclonal Antibody

Applications

Application Tested Dilution Publications
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL -

Product Specifications

Property Description
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant Human CPSF1. Recombinant protein control fragment (Product #RP-107662)
Conjugate Unconjugated
Form Liquid
Concentration 0.05 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% 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_2663196

Product Specific Information

Immunogen sequence:
AISLNITQKVH PVIWSLTSLP FDCTQALAVP KPIGGVVVFA VNSLLYLNQS VPPYGVALNS LTTGTTAFPL RT

Highest antigen sequence identity to the following orthologs:

  • Mouse: 99%
  • Rat: 99%

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, and one RING-type zinc finger.
It is believed to have E3 ubiquitin ligase activity which targets the catalytic subunit of protein phosphatase 2 for degradation.
This cytoplasmic protein is found as a homodimer or heterodimer with Midline-2 and interacts with IGBP1 (Lymphocyte signaling protein A4).
Defects in MID1 are the cause of Opitz syndrome type I (OS-I), an X-linked recessive disorder characterized by hypertelorism, genitourinary defects, cleft lip/palate, 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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