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Thermo Fisher Scientific QKI Monoclonal Antibody (N147/6), APC
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Thermo Fisher Scientific QKI Monoclonal Antibody (N147/6), APC

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Thermo Fisher QKI Monoclonal Antibody (N147/6), APC은 인간, 마우스, 랫트 QKI 단백질을 검출하는 고특이적 항체입니다. Western blot, IHC, ICC/IF에 사용 가능하며 APC 형광 표지로 651/660 nm 파장에서 검출됩니다. 단백질 G 정제, 무보존제, 4°C 보관.

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마지막 업데이트 2025. 08. 05. 오후 02:44
Thermo Fisher Scientific MA545689 QKI Monoclonal Antibody (N147/6), APC 100 ug pk판매 단위 pk ·
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663,800원VAT 포함 730,180원

Thermo Fisher Scientific · Thermo Fisher Scientific QKI Monoclonal Antibody (N147/6), APC

Applications

  • Western Blot (WB): 1:1,000
  • Immunohistochemistry (IHC): Assay-dependent
  • Immunocytochemistry (ICC/IF): Assay-dependent

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Clone N147/6
Immunogen Fusion protein amino acids 1–341 (full-length) of human QKI-5
Conjugate APC
Excitation / Emission Max 651 / 660 nm
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer 95.64 mM phosphate / 2.48 mM MES, pH 7.4, with 0.5 M EDTA
Contains No preservative
Storage Conditions 4°C
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2932143

Additional Formats

  • Unconjugated (MA5-27651)
  • FITC (MA5-45690)
  • PE (MA5-45692)
  • PerCP (MA5-45691)
  • Request custom conjugation

Product Specific Information

  • Mouse: 100% identity (341/341 amino acids identical)
  • Rat: 99% identity (339/341 amino acids identical)
  • 90% identity with QKI-6, QKI-7, and QKI-7b

  • 1 µg/mL of MA5-45689 detects Pan-QKI in 20 µg of rat brain lysate by colorimetric immunoblot using Goat anti-mouse IgG:HRP as secondary antibody
  • Detects approximately 36–38 kDa
  • Formerly sold as clone S147-6

Target Information

This gene encodes the sacsin protein, containing UbL, DnaJ, and HEPN domains. It is highly expressed in the central nervous system, also found in skin, skeletal muscle, and pancreas. Mutations cause autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS), a neurodegenerative disorder with cerebellar ataxia and spasticity. Sacsin protects against mutant ataxin-1. A pseudogene exists on chromosome 11. Alternative splicing results in multiple transcript variants.


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


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