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Thermo Fisher Scientific HSP27 Monoclonal Antibody (G3.1)
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Thermo Fisher Scientific HSP27 Monoclonal Antibody (G3.1)

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HSP27 단백질을 특이적으로 인식하는 Mouse IgG1 단일클론 항체. Western blot, ELISA, IP 등 다양한 응용에 적합. Human 시료에 반응하며, 단백질 A로 정제된 액상 형태로 제공. -20°C에서 안정적으로 보관 가능.

카탈로그번호
200-301-243
판매단위
pk
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마지막 업데이트 2025. 07. 29. 오후 06:46
Thermo Fisher Scientific 200-301-243 HSP27 Monoclonal Antibody (G3.1) 100 ug pk판매 단위 pk ·
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683,300원VAT 포함 751,630원

Thermo Fisher Scientific · Thermo Fisher Scientific HSP27 Monoclonal Antibody (G3.1)

Applications

Western Blot (WB)

  • Tested Dilution: 1:500–1:1,000

ELISA

  • Tested Dilution: 1:10,000–1:50,000

Immunoprecipitation (IP)

  • Tested Dilution: 1:500–1:1,000

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG1, kappa
Class Monoclonal
Type Antibody
Clone G3.1
Immunogen Produced by repeated immunizations with a prokaryotic recombinant protein corresponding to the full-length human HSP27 protein
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
Storage Buffer 0.02M potassium phosphate, pH 7.2, with 0.5M NaCl
Contains 0.01% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • Store vial at -20°C prior to opening.
  • Aliquot contents and freeze at -20°C or below for extended storage.
  • Avoid cycles of freezing and thawing.
  • Centrifuge product if not completely clear after standing at room temperature.
  • Stable for several weeks at 4°C as an undiluted liquid.
  • Dilute only prior to immediate use.

Reacts specifically with HSP27 in human tissues and cell lines. MCF-7 cells are recommended as a positive control.
Cross-reactivity with HSP27 from other mammalian sources is likely.
No cross-reactivity occurs with HSP70, HSP90, or HSP104.


Target Information

In response to environmental stress, cells increase expression of heat shock proteins.
HSPB1 (heat shock protein beta-1 or HSP27) is a small molecular chaperone that maintains denatured proteins in a folding-competent state.
It contributes to stress resistance and actin organization, and regulates phosphorylation and axonal transport of neurofilament proteins.
Mutations in the HSPB1 gene can result in Charcot-Marie-Tooth disease 2F and distal hereditary motor neuronopathy type 2B.


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

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