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Thermo Fisher Scientific PSMA1 Polyclonal Antibody
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Thermo Fisher Scientific PSMA1 Polyclonal Antibody

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Thermo Fisher Scientific의 PSMA1 Polyclonal Antibody는 인간 PSMA1 단백질을 인식하는 토끼 유래 IgG 항체로, WB, IHC, IP 등 다양한 응용에 적합합니다. 항원 친화 크로마토그래피로 정제되었으며, 4°C에서 보관합니다. 연구용으로만 사용 가능합니다.

카탈로그번호
A303846A
판매단위
pk
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마지막 업데이트 2025. 08. 03. 오후 11:57
Thermo Fisher Scientific A303846A PSMA1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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658,900원VAT 포함 724,790원

Thermo Fisher Scientific · Thermo Fisher Scientific PSMA1 Polyclonal Antibody

Applications

Application Tested Dilution
Western Blot (WB) 1:2,000–1:10,000
Immunohistochemistry (IHC) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:500–1:2,000
Immunoprecipitation (IP) 2–10 µg/mg lysate

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Region between residue 213 and 263 of Human Proteasome (Prosome, Macropain) Subunit, Alpha Type, 1
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer Phosphate/tris citrate, pH 7–8
Contains 0.09% sodium azide
Storage Conditions 4°C
Shipping Conditions Wet ice

Product Specific Information

  • Recommended shelf life: 1 year from date of receipt
  • For IHC: Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections
  • Predicted to react with Bovine and Orangutan based on 100% sequence identity

Target Information

Proteolytic degradation is essential for maintaining appropriate levels of short-lived and regulatory proteins involved in cellular metabolism, stress response, antigen presentation, receptor modulation, cell cycle regulation, transcription, and signaling.
The ubiquitin-proteasome pathway degrades most cytosolic and nuclear proteins, while others are processed via the vacuolar pathway (endosomes, lysosomes, endoplasmic reticulum).
The 26S proteasome is an ATP-dependent, multisubunit (~31), barrel-shaped molecular machine (~2.5 MDa) composed of a 20S core complex capped by one or two 19S regulatory subunits.
The 19S subunits recognize ubiquitinated proteins and facilitate unfolding and translocation into the 20S lumen.
Defects in the ubiquitin-proteasome pathway are linked to genetic diseases such as cystic fibrosis, Angelman’s syndrome, and Liddle syndrome.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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