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Thermo Fisher Scientific HSP60 (Heat Shock Protein 60) (Mitochondrial Marker) Monoclonal Antibody (LK2)
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Thermo Fisher Scientific HSP60 (Heat Shock Protein 60) (Mitochondrial Marker) Monoclonal Antibody (LK2)

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HSP60 미토콘드리아 마커 단클론 항체(LK2)는 다양한 종에 반응하며, Western blot, IHC, ICC 등 다중 응용에 적합합니다. 단일클론 Mouse IgG1 항체로, 단백질 접힘 연구 및 세포 내 단백질 표지에 유용합니다. 연구용으로만 사용 가능합니다.

카탈로그번호
3329-MSM2-P1ABX
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 04:26
Thermo Fisher Scientific 3329-MSM2-P1ABX HSP60 (Heat Shock Protein 60) (Mitochondrial Marker) Monoclonal Antibody (LK2) 100 ug pk판매 단위 pk ·
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900,300원VAT 포함 990,330원

Thermo Fisher Scientific · Thermo Fisher Scientific HSP60 (Heat Shock Protein 60) (Mitochondrial Marker) Monoclonal Antibody (LK2)

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1–2 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) Assay-dependent
Immunohistochemistry (PFA fixed) (IHC (PFA)) 1–2 µg/mL
Immunocytochemistry (ICC/IF) 2–4 µg/mL

Product Specifications

Specification Description
Species Reactivity Bacteria, Chicken, Guinea pig, Hamster, Human, Mouse, Non-human primate, Nematode, Plant, Rat, Yeast
Host / Isotype Mouse / IgG1, kappa
Class Monoclonal
Type Antibody
Clone LK2
Immunogen Recombinant human HSP60 protein
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A/G
Storage Buffer PBS, pH 7.4
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

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. This protein is essential for the folding and assembly of newly imported proteins in the mitochondria. This gene is adjacent to a related family member, and the region between the two genes functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Two transcript variants encoding the same protein have been identified for this gene. Mutations associated with 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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