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Thermo Fisher Scientific HSP60 (Heat Shock Protein 60) Recombinant Rabbit Monoclonal Antibody (HSPD1, 6496R)
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Thermo Fisher Scientific HSP60 (Heat Shock Protein 60) Recombinant Rabbit Monoclonal Antibody (HSPD1, 6496R)

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HSP60 단백질을 인식하는 재조합 토끼 단클론 항체로, Western blot 및 IHC(P)에서 1–2 µg/mL 농도로 사용 가능. 다양한 종에 반응하며, HEK293 발현 시스템에서 생산된 IgG 형 항체. 단백질 A/G 정제, PBS(pH 7.4) 용액에 보존.

카탈로그번호
3329-RBM13-P1ABX
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 09:35
Thermo Fisher Scientific 3329-RBM13-P1ABX HSP60 (Heat Shock Protein 60) Recombinant Rabbit Monoclonal Antibody (HSPD1, 6496R) 100 ug pk판매 단위 pk ·
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975,200원VAT 포함 1,072,720원

Thermo Fisher Scientific · Thermo Fisher Scientific HSP60 (Heat Shock Protein 60) Recombinant Rabbit Monoclonal Antibody (HSPD1, 6496R)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1–2 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 1–2 µg/mL

Product Specifications

항목 내용
Species Reactivity Bovine, Dog, Chicken, Hamster, Human, Mouse, Non-human primate, Sheep, Pig, Rabbit, Rat
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone HSPD1, 6496R
Immunogen Recombinant human full-length 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 or -80°C if preferred
Shipping conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • Immunohistochemistry (PFA fixed):
    Incubate antibody for 30 minutes at room temperature.
    Staining of formalin-fixed tissues requires heating tissue sections in 10 mM Tris with 1 mM EDTA, pH 9.0, for 45 minutes at 95°C, followed by cooling at room temperature for 20 minutes.

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 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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