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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(Recombinant Rabbit Monoclonal Antibody)은 다양한 종에 반응하는 고특이성 항체로 Western blot 및 IHC(P) 실험에 적합합니다. HEK293 발현 시스템에서 생산된 재조합 항체로 안정적인 액상 형태이며, 단백질 접힘 연구 및 미토콘드리아 단백질 분석에 활용됩니다.

카탈로그번호
3329-RBM13-P1
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 09:35
Thermo Fisher Scientific 3329-RBM13-P1 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 200 µg/mL
Purification Protein A/G
Storage Buffer PBS, pH 7.4, with 0.05% BSA
Contains 0.05% sodium azide
Storage Conditions 4°C
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 and is essential for the folding and assembly of newly imported proteins in the mitochondria. The gene region functions as a bidirectional promoter between two related family members. Several pseudogenes are associated with this gene, and 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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