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Thermo Fisher Scientific Pan Ras Polyclonal Antibody
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Thermo Fisher Scientific Pan Ras Polyclonal Antibody

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Thermo Fisher Scientific의 Pan Ras Polyclonal Antibody는 인간 및 다양한 종에서 Ras 단백질을 검출하기 위한 항체로, WB, IHC, ICC/IF에 적합합니다. 항원 친화 크로마토그래피로 정제되었으며, 고순도 액상 형태로 제공됩니다. 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 05. 오전 12:25
Thermo Fisher Scientific PA578035 Pan Ras Polyclonal Antibody 100 ul pk판매 단위 pk ·
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754,700원VAT 포함 830,170원

Thermo Fisher Scientific · Thermo Fisher Scientific Pan Ras Polyclonal Antibody

Applications

Application Tested Dilution
Western Blot (WB) 1:500–1:10,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:100–1:1,000
Immunocytochemistry (ICC/IF) 5 µg/mL

Product Specifications

항목 내용
Species Reactivity Amphibian, Human, Rodent, Rat, Zebrafish
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Carrier-protein conjugated synthetic peptide encompassing a sequence within the N-terminus region of human KRAS. The exact sequence is proprietary.
Conjugate Unconjugated
Form Liquid
Concentration 0.27 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7, with 20% glycerol, 1% BSA
Contains 0.025% ProClin 300
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_2736317

Product Specific Information

  • Positive Control: A549, H1299, HCT116, KRAS, HRAS, NRAS, zebrafish liver, zebrafish GI, whole zebrafish
  • Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

Target Information

This gene belongs to the Ras oncogene family, whose members are related to the transforming genes of mammalian sarcoma retroviruses. The products encoded by these genes function in signal transduction pathways. These proteins can bind GTP and GDP, and they have intrinsic GTPase activity. This protein undergoes a continuous cycle of de- and re-palmitoylation, which regulates its rapid exchange between the plasma membrane and the Golgi apparatus. Mutations in this gene cause Costello syndrome, characterized by prenatal overgrowth, postnatal growth deficiency, tumor predisposition, mental retardation, and distinctive facial and cardiovascular abnormalities. Defects in this gene are implicated in various cancers, including bladder cancer, follicular thyroid cancer, and oral squamous cell carcinoma. Multiple transcript variants encoding different isoforms have been identified.

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

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