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Thermo Fisher Scientific QKI Monoclonal Antibody (GT1589)
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Thermo Fisher Scientific QKI Monoclonal Antibody (GT1589)

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QKI 단백질을 검출하기 위한 Thermo Fisher Scientific의 마우스 단클론 항체로, WB, IHC, ICC 등 다양한 응용에 적합합니다. 인간, 마우스, 랫트 반응성이 있으며, 단백질 A로 정제된 액상 형태입니다. 단기 4°C, 장기 -20°C 보관 권장.

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pk
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마지막 업데이트 2025. 08. 05. 오전 12:04
Thermo Fisher Scientific MA527804 QKI Monoclonal Antibody (GT1589) 100 ul pk판매 단위 pk ·
재고 확인 필요
731,200원VAT 포함 804,320원

Thermo Fisher Scientific · Thermo Fisher Scientific QKI Monoclonal Antibody (GT1589)

Thermo Fisher Scientific QKI Monoclonal Antibody (GT1589)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:1,000–1:10,000
Immunohistochemistry (Paraffin) (IHC-P) 1:100–1:1,000
Immunohistochemistry (Frozen) (IHC-F) 1:100–1:1,000
Immunocytochemistry (ICC/IF) 1:100–1:1,000

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone GT1589
Immunogen Recombinant protein encompassing a sequence within the center region of human QKI (exact sequence proprietary)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
Storage Buffer PBS
Contains No preservative
Storage Conditions Store at 4°C short term; for long term, store at -20°C and avoid freeze/thaw cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2735340

Product Specific Information

  • Positive Control: 293T
  • Predicted Reactivity: Xenopus laevis (93%), Dog (100%), Cat (100%), Pig (100%), Chicken (98%), Bovine (100%)
  • Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

Target Information

This gene encodes the sacsin protein, which includes a UbL domain at the N-terminus, a DnaJ domain, and a HEPN domain at the C-terminus. The gene is highly expressed in the central nervous system, also found in skin, skeletal muscles, and at low levels in the pancreas. This gene includes a very large exon spanning more than 12.8 kb. Mutations in this gene result in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS), a neurodegenerative disorder characterized by early-onset cerebellar ataxia with spasticity and peripheral neuropathy. Sacsin has been found to protect against mutant ataxin-1. A pseudogene associated with this gene is located on chromosome 11. Alternative splicing of this gene results in multiple transcript variants.

Usage Note

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

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