CacheBy
Thermo Fisher Scientific Human AIF Synthetic Peptide
원본

Thermo Fisher Scientific Human AIF Synthetic Peptide

상품 한눈에 보기

인간 AIF 단백질의 N-말단 14개 아미노산에 해당하는 합성 펩타이드입니다. 항체 PA5-19947의 차단 펩타이드로 사용 가능합니다. PBS 버퍼에 0.1% BSA 및 0.02% sodium azide 포함. -20°C에서 보관.

카탈로그번호
PEP0072
카테고리
Protein
판매단위
pk
카탈로그 보기

카탈로그

1개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
마지막 업데이트 2025. 07. 03. 오후 07:03
Thermo Fisher Scientific PEP0072 Human AIF Synthetic Peptide 50 ug pk판매 단위 pk ·
재고 확인 필요
200,000원VAT 포함 220,000원

Thermo Fisher Scientific · Thermo Fisher Scientific Human AIF Synthetic Peptide

Applications

Control (Ctrl)

  • Assay-dependent

Blocking Assay (BLOCK)

  • Assay-dependent

Product Specifications

항목 내용
Species Reactivity Human
Class Synthetic
Type Peptide
Conjugate Unconjugated
Form Liquid
Concentration 200 µg/mL
Purification Purified
Storage Buffer PBS, pH 7.2, with 0.1% BSA
Contains 0.02% sodium azide
Storage Conditions -20°C

Product Specific Information

This peptide corresponds to the 14 amino acid N-terminus of human AIF.
PEP-0072 can be used as a blocking peptide with polyclonal antibody PA5-19947.

Target Information

Apoptosis Inducing Factor (AIF) causes chromatin condensation and DNA fragmentation. AIF was recently identified and cloned. Apoptosis is characterized by several morphological nuclear changes including chromatin condensation and nuclear fragmentation. These changes are triggered by the activation of members of the caspase family, caspase-activated DNase, and several novel proteins.

Like the critical molecules cytochrome c and caspase-9 in apoptosis, AIF localizes in mitochondria. AIF translocates to the nucleus when apoptosis is induced and induces mitochondria to release the apoptogenic proteins cytochrome c and caspase-9. AIF induces chromatin condensation and large-scale DNA fragmentation, which are the hallmarks of apoptosis, in both isolated nuclei and live cells under apoptotic stimuli.

AIF is highly conserved between human and mouse and is widely expressed. Mutations in the AIF gene cause combined oxidative phosphorylation deficiency 6, resulting in severe mitochondrial encephalomyopathy. Alternative splicing results in multiple transcript variants of AIF, and a related pseudogene has been identified on chromosome 10.


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.