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Thermo Fisher Scientific HSP60 Monoclonal Antibody (3G8)
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Thermo Fisher Scientific HSP60 Monoclonal Antibody (3G8)

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HSP60 단백질을 검출하기 위한 Thermo Fisher Scientific의 단클론 항체. Western blot, IHC, ICC/IF, Flow cytometry, ELISA 등 다양한 응용에 적합. 사람, 마우스, 비인간 영장류, 랫트 시료에 반응. 비결합(Unconjugated) 형태로 제공되며, 냉장 또는 냉동 보관 권장.

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마지막 업데이트 2025. 08. 03. 오후 04:24
Thermo Fisher Scientific MA515836 HSP60 Monoclonal Antibody (3G8) 100 ul pk판매 단위 pk ·
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760,500원VAT 포함 836,550원

Thermo Fisher Scientific · Thermo Fisher Scientific HSP60 Monoclonal Antibody (3G8)

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:200–1:1,000
Immunocytochemistry (ICC/IF) 1:100–1:1,000
Flow Cytometry (Flow) 1:200–1:400
ELISA 1:10,000

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Non-human primate, Rat
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone 3G8
Immunogen Purified recombinant fragment of human HSP60 expressed in E. coli
Conjugate Unconjugated
Form Liquid
Concentration Not determined
Storage Buffer Ascites
Contains 0.03% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_11155172

Product Specific Information

MA5-15836 targets HSP60 in indirect ELISA, FACS, IF, IHC, and WB applications and shows reactivity with human, mouse, non-human primate, and rat samples.
The immunogen is a purified recombinant fragment of human HSP60 expressed in E. coli.
MA5-15836 detects HSP60 with a predicted molecular weight of approximately 61 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 and is essential for the folding and assembly of newly imported proteins in mitochondria.
The 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.
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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