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Thermo Fisher Scientific Ataxin 1 Monoclonal Antibody (N76/8)
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Thermo Fisher Scientific Ataxin 1 Monoclonal Antibody (N76/8)

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Ataxin 1 단백질 검출용 Thermo Fisher Scientific의 Mouse Monoclonal Antibody (Clone N76/8). Western blot, IHC, ICC, IP에 적합하며 Human, Mouse, Rat 반응성. Protein G 정제, 1 mg/mL 농도, -20°C 보관.

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마지막 업데이트 2025. 08. 03. 오후 10:58
Thermo Fisher Scientific MA527666 Ataxin 1 Monoclonal Antibody (N76/8) 100 ug pk판매 단위 pk ·
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775,200원VAT 포함 852,720원

Thermo Fisher Scientific · Thermo Fisher Scientific Ataxin 1 Monoclonal Antibody (N76/8)

Thermo Fisher Scientific Ataxin 1 Monoclonal Antibody (N76/8)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:1,000
Immunohistochemistry (PFA fixed) (IHC (PFA)) 1:100
Immunocytochemistry (ICC/IF) 1:100
Immunoprecipitation (IP) Assay-Dependent

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Clone N76/8
Immunogen Synthetic peptide amino acids 164–197 (ATTPSQRSQLEAYSTLLANMGSLSQAPGHKVEPP) of mouse Ataxin-1. Rat: 100% identity (34/34 amino acids identical). Human: 88% identity (30/34 amino acids identical).
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer PBS, pH 7.4, with 50% glycerol
Contains 0.1% sodium azide
Storage Conditions -20°C
Shipping Conditions Wet ice
RRID AB_2735120

Additional Formats

Product Specific Information

  • 1 µg/mL of MA5-27666 detects Ataxin-1 in 20 µg of rat brain lysate by colorimetric immunoblot using Goat anti-mouse IgG:HRP as secondary antibody.
  • Detects approximately 85 kDa.
  • Formerly sold as clone S76-8.

Target Information

The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem, and spinal cord.
ADCA is divided into three groups (types I–III). ADCAI is genetically heterogeneous, with loci SCA1, 2, 3, 4, and 6 on different chromosomes. ADCAII (SCA7) presents with retinal degeneration, and ADCAIII (SCA5) is a pure cerebellar syndrome.
These diseases are caused by expansion of CAG repeats, resulting in elongated polyglutamine tracts. The function of ataxins is not fully known. The SCA1 locus is mapped to chromosome 6, with diseased alleles containing 41–81 CAG repeats versus 6–39 in normal alleles.
At least two transcript variants encoding the same protein have been identified.

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

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