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Thermo Fisher Scientific HSP27 Monoclonal Antibody (5D12-A12), PerCP
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Thermo Fisher Scientific HSP27 Monoclonal Antibody (5D12-A12), PerCP

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HSP27 단백질을 인식하는 PerCP 결합 단클론 항체로, WB, IHC, ICC, ELISA, IP 등 다양한 응용에 적합. 사람 시료 반응성, 단클론(Mouse IgG2b) 형식. 27kDa 단백질 검출에 특이적이며 Alpha B crystallin과 교차반응 없음. 연구용으로만 사용 가능.

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마지막 업데이트 2025. 08. 04. 오전 06:28
Thermo Fisher Scientific MA545207 HSP27 Monoclonal Antibody (5D12-A12), PerCP 200 ug pk판매 단위 pk ·
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663,800원VAT 포함 730,180원

Thermo Fisher Scientific · Thermo Fisher Scientific HSP27 Monoclonal Antibody (5D12-A12), PerCP

Applications and Tested Dilutions

Application Tested Dilution Notes
Western Blot (WB) 1:2,000
Immunohistochemistry (IHC) Assay-dependent
Immunocytochemistry (ICC/IF) 1:100
ELISA Assay-dependent
Immunoprecipitation (IP) Assay-dependent

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Mouse / IgG2b, kappa
Class Monoclonal
Type Antibody
Clone 5D12-A12
Immunogen Full length human HSP27 (UniProt ID: P04792-1, antigen range: 1–205)
Conjugate PerCP
Excitation / Emission Max 482 / 675 nm
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer 95.64 mM phosphate / 2.48 mM MES, pH 7.2, with 0.5 M EDTA
Contains No preservative
Storage Conditions 4°C
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2931661

Available Formats


Product Specific Information

  • 0.5 µg/mL of MA5-45207 was sufficient for detection of HSP27 in 10 µg of HeLa lysate by colorimetric immunoblot using Goat anti-mouse IgG:HRP as the secondary antibody.
  • Detects approximately 27 kDa.
  • No cross-reactivity to Alpha B crystallin.
  • Very limited cross-reactivity to other species.

Target Information

HSPB1 (heat shock protein beta-1 or HSP27) is a small heat shock protein acting as a molecular chaperone that maintains denatured proteins in a folding-competent state. It plays roles in stress resistance and actin organization. Through its chaperone activity, HSP27 regulates biological processes including phosphorylation and axonal transport of neurofilament proteins.
Mutations in the HSPB1 gene can cause Charcot-Marie-Tooth disease type 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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