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Thermo Fisher Scientific QKI Recombinant Rabbit Monoclonal Antibody (1D1N6)
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Thermo Fisher Scientific QKI Recombinant Rabbit Monoclonal Antibody (1D1N6)

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QKI 단백질을 인식하는 토끼 유래 재조합 단클론 항체로, Western blot, IHC, ICC, ELISA, IP에 적합합니다. 인간, 생쥐, 랫트 시료에 반응하며, HEK293 세포에서 발현되었습니다. 액상 형태로 제공되며 -20°C에서 보관합니다.

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마지막 업데이트 2025. 08. 04. 오후 02:39
Thermo Fisher Scientific MA542589 QKI Recombinant Rabbit Monoclonal Antibody (1D1N6) 100 ul pk판매 단위 pk ·
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714,600원VAT 포함 786,060원

Thermo Fisher Scientific · Thermo Fisher Scientific QKI Recombinant Rabbit Monoclonal Antibody (1D1N6)

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:1,000
Immunohistochemistry (Paraffin) (IHC-P) 1:50–1:200
Immunocytochemistry (ICC/IF) 1:50–1:200
ELISA 1 µg/mL
Immunoprecipitation (IP) 0.5–4 µg antibody for 200–400 µg extracts

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone 1D1N6
Immunogen Synthetic peptide corresponding to amino acids 242–341 of human QKI (UniProt ID: Q96PU8)
Conjugate Unconjugated
Form Liquid
Concentration 0.8 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol, 0.05% BSA
Contains 0.02% sodium azide
Storage Conditions -20°C; avoid freeze/thaw cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2911730

Product Specific Information

  • Positive test controls: SKOV3, NIH/3T3, U-251MG, Neuro-2a, Mouse brain, Rat brain, Rat heart
  • Subcellular localization: Cytoplasm, Nucleus

Immunogen sequence:
RTPTPAGPTI MPLIRQIQTA VMPNGTPHPT AAIVPPGPEA GLIYTPYEYP YTLAPATSIL EYPIEPSGVL GAVATKVRRH DMRVHPYQRI VTADRAATGN

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. It is highly expressed in the central nervous system, and also found in skin, skeletal muscles, and at low levels in the pancreas. The gene includes a large exon spanning more than 12.8 kb. Mutations in this gene cause autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS), a neurodegenerative disorder characterized by early-onset cerebellar ataxia with spasticity and peripheral neuropathy. Sacsin protects against mutant ataxin-1. A pseudogene is located on chromosome 11, and 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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