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Thermo Fisher Scientific ASAH1 Polyclonal Antibody
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Thermo Fisher Scientific ASAH1 Polyclonal Antibody

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Human ASAH1 단백질에 특이적인 Rabbit Polyclonal Antibody로, WB 및 IHC(P)에서 검증됨. 항원 친화 크로마토그래피로 정제된 액상 형태이며, 장기 보관 시 -20°C에서 안정적. 암 연구 및 리소좀 대사 관련 연구에 적합.

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마지막 업데이트 2025. 08. 04. 오후 02:20
Thermo Fisher Scientific PA552150 ASAH1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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754,700원VAT 포함 830,170원

Thermo Fisher Scientific · Thermo Fisher Scientific ASAH1 Polyclonal Antibody

Thermo Fisher Scientific ASAH1 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution Publications
Western Blot (WB) 0.04–0.4 µg/mL View 1 publication
Immunohistochemistry (Paraffin) (IHC (P)) 1:500–1:1,000 View 1 publication

Product Specifications

항목 내용
Species Reactivity Human
Published Species Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human ASAH1 (Product #RP-88819)
Conjugate Unconjugated
Form Liquid
Concentration 0.1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% 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_2638263

Product Specific Information

Immunogen sequence:
ENSTSYEEAK NLLTKTKILA PAYFILGGNQ SGEGCVITRD RKESLDVYEL DAKQGRWYVV QTNYDRWKHP FFLDDRRTPA KMCLNRTSQE NISFETMYDV LSTKPVLNKL TVYTTLIDVT KGQF

Highest antigen sequence identity to orthologs:

  • Mouse: 82%
  • Rat: 86%

Target Information

ASAH1 encodes a member of the acid ceramidase family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. The processing of this preproprotein generates alpha and beta subunits that heterodimerize to form the mature lysosomal enzyme, which catalyzes the degradation of ceramide into sphingosine and free fatty acid.

This enzyme is overexpressed in multiple human cancers and may play a role in cancer progression. Mutations in ASAH1 are associated with lysosomal storage disorder Farber lipogranulomatosis and neuromuscular disorder spinal muscular atrophy with progressive myoclonic epilepsy.

Related Pathways:

  • Innate Immune System
  • Sphingolipid Metabolism

Associated Diseases:

  • Farber Lipogranulomatosis
  • Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy

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

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