CacheBy
Thermo Fisher Scientific Huntingtin Polyclonal Antibody
원본

Thermo Fisher Scientific Huntingtin Polyclonal Antibody

상품 한눈에 보기

Huntingtin 단백질을 인식하는 Rabbit Polyclonal Antibody로, 인간 및 생쥐 시료의 WB, IHC, ICC, ELISA에 사용 가능. Caspase 절단 부위(513 aa) 특이적 인식. 액상 형태로 -20°C 보관. 연구용으로만 사용.

카탈로그번호
PA1002
판매단위
pk
카탈로그 보기

카탈로그

1개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
마지막 업데이트 2025. 08. 04. 오후 05:55
Thermo Fisher Scientific PA1002 Huntingtin Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
586,500원VAT 포함 645,150원

Thermo Fisher Scientific · Thermo Fisher Scientific Huntingtin Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution Publications
Western Blot (WB) 1:500–1:1,000 View 1 publication
Immunohistochemistry (IHC) 1:50–1:200 -
Immunocytochemistry (ICC/IF) 1:50–1:200 -
ELISA 1:20–1:100 -

Product Specifications

Specification Description
Published species Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide conjugated to KLH via cysteine corresponding to residues HTLQADSVD (505–513) of Human HTT
Conjugate Unconjugated
Form Liquid
Concentration 0.13 mg/mL
Storage conditions -20°C
Shipping conditions Ambient (domestic); Wet ice (international)
RRID AB_2539849

Product Specific Information

PA1-002 antibody has been validated for use in ELISA, Western Blot, immunofluorescence, and immunohistochemistry with human and mouse samples.

Neoepitope antibodies distinguish cleaved or processed protein fragments from full-length proteins by targeting specific cleavage sites.
Human HTT caspase cleavage sites generate fragment-specific forms of the protein. Caspase-3/7 cleaves at amino acids 513 and 552, caspase-2 at 552, and caspase-6 at 586.
Neo-specific antibody PA1-002 recognizes the 513-cleaved fragment of Huntingtin without detecting the full-length form.


Target Information

Huntingtin is a disease gene associated with Huntington’s disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons.
HD results from expanded, unstable trinucleotide repeats in the huntingtin gene, producing a polyglutamine stretch in the protein.
It is an autosomal dominant disorder with mid-life onset, presenting with psychiatric symptoms, dementia, and involuntary movements (chorea), leading to death within 10–20 years.

The huntingtin locus spans approximately 180 kb with 67 exons. It is expressed as two alternatively polyadenylated transcripts (~13.7 kb and ~10.3 kb) with tissue-specific abundance.
The gene is essential for normal development and widely expressed in fetal and adult tissues.


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

Thermo Fisher Scientific 상품 둘러보기

전체보기

문의

0

아직 등록된 문의가 없어요.