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Thermo Fisher Scientific HSP60 (Heat Shock Protein 60) (Mitochondrial Marker) Monoclonal Antibody (HSPD1/780)
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Thermo Fisher Scientific HSP60 (Heat Shock Protein 60) (Mitochondrial Marker) Monoclonal Antibody (HSPD1/780)

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HSP60 단백질을 인식하는 미토콘드리아 마커 단일클론 항체로, WB, IHC, ICC, Flow 등 다양한 응용에 적합. 인간 및 여러 종에서 반응하며, 단백질 접힘 및 면역 신호 연구에 유용. 연구용으로만 사용 가능.

카탈로그번호
3329-MSM4-P1ABX
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 08:04
Thermo Fisher Scientific 3329-MSM4-P1ABX HSP60 (Heat Shock Protein 60) (Mitochondrial Marker) Monoclonal Antibody (HSPD1/780) 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 (HSPD1/780)

Thermo Fisher Scientific HSP60 (Heat Shock Protein 60) (Mitochondrial Marker) Monoclonal Antibody (HSPD1/780)

Applications and Tested Dilution

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) 1–2 µg/mL
Flow Cytometry (Flow) 1–2 µg/10^6 cells
Peptide Array (Array) Assay-dependent

Product Specifications

Property Description
Species Reactivity Bovine, Dog, Chicken, Hamster, Human, Mouse, Non-human primate, Sheep, Pig, Rabbit, Rat
Host / Isotype Mouse / IgG1, kappa
Class Monoclonal
Type Antibody
Clone HSPD1/780
Immunogen Recombinant human HSPD1 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. The gene region between this and a related family member functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Two transcript variants encoding the same protein have been identified. 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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