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Thermo Fisher Scientific Atrophin 1 Polyclonal Antibody
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Thermo Fisher Scientific Atrophin 1 Polyclonal Antibody

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Human, Mouse, Rat 반응성의 Rabbit Polyclonal Atrophin 1 항체로 Western blot, ICC/IF, IP에 적합. 고순도(>95%) 항원 친화 크로마토그래피 정제. PBS/glycerol buffer에 보관하며 DRPLA 연구에 유용.

카탈로그번호
PA536927
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오전 03:43
Thermo Fisher Scientific PA536927 Atrophin 1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
630,500원VAT 포함 693,550원

Thermo Fisher Scientific · Thermo Fisher Scientific Atrophin 1 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 1:500–1:1,000

Immunocytochemistry (ICC/IF)

  • Tested Dilution: 1:50–1:200

Immunoprecipitation (IP)

  • Tested Dilution: 1:50–1:200

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to amino acids 135–180 of human Atrophin-1
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2553820

Product Specific Information

This antibody detects endogenous Atrophin 1 protein at a molecular weight of 150–180 kDa.
Purity is >95% by SDS-PAGE.


Target Information

Dentatorubral pallidoluysian atrophy (DRPLA) is a rare neurodegenerative disorder characterized by cerebellar ataxia, myoclonic epilepsy, choreoathetosis, and dementia.
The disorder is associated with the expansion of a trinucleotide repeat (CAG/CAA) within the Atrophin 1 gene—from 7–35 copies to 49–93 copies.
The encoded protein includes a serine repeat and regions of alternating acidic and basic amino acids, as well as a variable glutamine repeat.
Alternative splicing results in two transcript variants that encode the same protein.


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

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