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Thermo Fisher Scientific ARPP21 Polyclonal Antibody
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Thermo Fisher Scientific ARPP21 Polyclonal Antibody

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ARPP21 단백질을 인식하는 Thermo Fisher Scientific의 폴리클로날 항체로, Western blot에 최적화되어 있습니다. 인간 시료에 반응하며, 항원 친화 크로마토그래피로 정제되었습니다. 액상 형태로 4°C에서 보관하며 연구용으로 사용됩니다.

카탈로그번호
A305-677A
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오전 11:39
Thermo Fisher Scientific A305-677A ARPP21 Polyclonal Antibody 100 uL pk판매 단위 pk ·
재고 확인 필요
889,600원VAT 포함 978,560원

Thermo Fisher Scientific · Thermo Fisher Scientific ARPP21 Polyclonal Antibody

Thermo Fisher Scientific ARPP21 Polyclonal Antibody

Applications

  • Western Blot (WB)

Tested Dilution: 1:2,000–1:10,000
Publications: -


Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen A region between residue 1 to 50 of human cAMP-regulated phosphoprotein 21
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer Phosphate/Tris citrate, pH 7.0–8.0
Contains 0.09% sodium azide
Storage Conditions 4°C
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Predicted reactivity by homology: Orangutan.


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. Clinically, ADCA has been divided into three groups: ADCA types I–III.
ADCAI is genetically heterogeneous, with five genetic loci—spinocerebellar ataxia (SCA) 1, 2, 3, 4, and 6—assigned to different chromosomes.
ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII, often referred to as the ‘pure’ cerebellar syndrome (SCA5), are most likely homogeneous disorders.
Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by expansion of these repeats, producing an elongated polyglutamine tract in the corresponding protein.
The expanded repeats are variable in size and unstable, usually increasing when transmitted to successive generations. The function of the ataxins is not known.
This locus has been mapped to chromosome 6, and the diseased allele contains 41–81 CAG repeats compared to 6–39 in the normal allele, associated with spinocerebellar ataxia type 1 (SCA1).
At least two transcript variants encoding the same protein have been found for this gene.


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


제품 이미지

(이미지 파일: A305-677A_ARPP21_Q9UBL0-1_Rabbit.svg, A305-677A_ARPP21_Q9UBL0-1_Rabbit_PDP.jpeg)

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