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Thermo Fisher Scientific C2 Monoclonal Antibody (269716)
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Thermo Fisher Scientific C2 Monoclonal Antibody (269716)

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인간 C2 단백질을 인식하는 Mouse IgG2a 단클론 항체입니다. Western blot 및 Immunoprecipitation에 적합하며 비특이적 반응이 없습니다. 동결건조 형태로 제공되며 -20°C에서 보관합니다. 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 07. 27. 오전 03:28
Thermo Fisher Scientific MA523970 C2 Monoclonal Antibody (269716) 100 ug pk판매 단위 pk
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644,200원VAT 포함 708,620원

Thermo Fisher Scientific · Thermo Fisher Scientific C2 Monoclonal Antibody (269716)

Applications

Western Blot (WB)

  • Tested Dilution: 1 µg/mL

Immunoprecipitation (IP)

  • Tested Dilution: 25 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Clone 269716
Immunogen Mouse myeloma cell line NS0-derived recombinant human Complement Component C2 (Ala21–Leu752)
Conjugate Unconjugated
Form Lyophilized
Concentration 0.5 mg/mL
Purification Protein A/G
Storage Buffer PBS with 5% trehalose
Contains No Preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2609687

Product Specific Information

  • In direct ELISAs, no cross-reactivity with recombinant human C1r, C1s, C3r, C5a, Factor B, or Factor I is observed.
  • In Western blots, this antibody recognizes rhC2 and rhC2B.
  • Reconstitute at 0.5 mg/mL in sterile PBS.

Target Information

Component C2 is a serum glycoprotein that functions as part of the classical pathway of the complement system. Activated C1 cleaves C2 into C2a and C2b. The serine proteinase C2a combines with complement factor 4b to form the C3 or C5 convertase.
Deficiency of C2 is associated with certain autoimmune diseases, and SNPs in this gene correlate with altered susceptibility to age-related macular degeneration.
This gene is located within the class III region of the MHC on chromosome 6. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

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

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