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Thermo Fisher Scientific HSP60 Monoclonal Antibody (LK2), PerCP
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Thermo Fisher Scientific HSP60 Monoclonal Antibody (LK2), PerCP

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HSP60 단백질을 검출하기 위한 PerCP 결합 단클론 항체. Western blot, IHC, Flow cytometry 등 다양한 응용 가능. 광범위한 종 반응성과 높은 특이성 제공. 연구용으로만 사용.

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마지막 업데이트 2025. 08. 04. 오후 11:36
Thermo Fisher Scientific MA545114 HSP60 Monoclonal Antibody (LK2), PerCP 200 ug pk판매 단위 pk ·
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Thermo Fisher Scientific · Thermo Fisher Scientific HSP60 Monoclonal Antibody (LK2), PerCP

Thermo Fisher Scientific HSP60 Monoclonal Antibody (LK2), PerCP

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:4,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:100
Immunohistochemistry (PFA fixed) (IHC (PFA)) 1:100
Flow Cytometry (Flow) Assay-dependent

Product Specifications

Property Description
Species Reactivity Bacteria, Bovine, Dog, Chicken, Fish, Guinea pig, Hamster, Human, Insect, Mouse, Non-human primate, Nematode, Plant, Pig, Rabbit, Rat, Yeast
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone LK2
Immunogen Recombinant human HSP60 (UniProt ID: P10809-1, antigen range: 383–419, antigen length: 573)
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 with 0.5 M EDTA
Contains No preservative
Storage Conditions 4°C
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2931568

Additional Formats

Product Specific Information

0.25 µg/mL of MA5-45114 was sufficient for detection of HSP60 in 10 µg of heat-shocked HeLa cell lysate by colorimetric immunoblot analysis using goat anti-mouse IgG as the secondary antibody. Detects approximately 60 kDa.

Target Information

This gene encodes a member of the chaperonin family. The encoded mitochondrial protein may function as a signaling molecule in the innate immune system. It is essential for the folding and assembly of newly imported proteins in mitochondria. The gene region acts as a bidirectional promoter between two related family members. Several pseudogenes have been identified, and two transcript variants encoding the same protein are known. Mutations in this gene cause autosomal recessive spastic paraplegia 13.

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

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