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Thermo Fisher Scientific HSP27 Recombinant Rabbit Monoclonal Antibody (155), FITC
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Thermo Fisher Scientific HSP27 Recombinant Rabbit Monoclonal Antibody (155), FITC

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FITC로 표지된 재조합 토끼 단일클론 항체로 인간 HSP27 단백질을 검출. 흐름세포분석(Flow Cytometry)에 적합하며, HEK293 세포에서 발현. 단백질 A로 정제된 액상 형태로 제공되며, 4°C 암소 보관. 연구용으로만 사용 가능.

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마지막 업데이트 2025. 08. 05. 오후 10:19
Thermo Fisher Scientific MA540990 HSP27 Recombinant Rabbit Monoclonal Antibody (155), FITC 100 tests pk판매 단위 pk ·
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Thermo Fisher Scientific · Thermo Fisher Scientific HSP27 Recombinant Rabbit Monoclonal Antibody (155), FITC

Thermo Fisher Scientific HSP27 Recombinant Rabbit Monoclonal Antibody (155), FITC

Applications

  • Flow Cytometry (Flow)

Tested Dilution: Assay-Dependent
Publications: -


Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone 155
Immunogen Recombinant Human HSP27 protein
Conjugate FITC
Excitation / Emission Max 498 / 517 nm
Form Liquid
Concentration 0.1 mg/mL
Purification Protein A
Storage Buffer PBS with 0.5% BSA
Contains 0.09% sodium azide
Storage Conditions 4°C, store in dark, DO NOT FREEZE
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2898751

Additional Formats


Product Specific Information

May be stored for twelve months without detectable loss of activity. Protect from prolonged exposure to light and do not freeze. Sodium azide is toxic to cells and should be disposed of properly by flushing with large volumes of water during disposal.


Target Information

In response to adverse changes in their environment, cells from many organisms increase the expression of a class of proteins referred to as heat shock or stress proteins.
HSPB1 (heat shock protein beta-1 or HSP27) is a small heat shock protein which functions as a molecular chaperone that maintains denatured proteins in a folding-competent state.
It plays a role in stress resistance and actin organization. Through its molecular chaperone activity, HSP27 regulates numerous biological processes including the phosphorylation and axonal transport of neurofilament proteins.
Mutations in the gene can result in Charcot-Marie-Tooth disease 2F and Neuronopathy distal hereditary motor 2B.


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


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