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Thermo Fisher Scientific Human Lass5 Synthetic Peptide
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Thermo Fisher Scientific Human Lass5 Synthetic Peptide

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인간 LASS5 단백질의 카복시 말단 17개 아미노산 서열을 기반으로 한 합성 펩타이드입니다. PA5-20569 폴리클로날 항체의 블로킹 펩타이드로 사용 가능합니다. 세라마이드 합성 연구 및 LASS5 관련 세포 성장 조절 실험에 적합합니다. 연구용으로만 사용됩니다.

판매단위
pk
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Thermo Fisher Scientific PEP0689 Human Lass5 Synthetic Peptide 50 ug pk판매 단위 pk
재고 확인 필요
195,500원VAT 포함 215,050원

Thermo Fisher Scientific · Thermo Fisher Scientific Human Lass5 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 17 amino acids near the carboxy terminus of human LASS5.
PEP-0689 can be used as a blocking peptide with polyclonal antibody PA5-20569.

Target Information

The LASS (longevity assurance homolog) family members represent a subgroup of the homeobox gene family and are highly conserved from yeasts to mammals. Six members of this family of proteins have been characterized (LASS1-6), and all are involved in ceramide synthesis during cell growth regulation and cancer differentiation.
LASS5, also called Trh4, is a 392-amino-acid endoplasmic reticulum multi-pass membrane protein. Functioning as a dihydro-ceramide synthase, LASS5 is involved in the production of sphingolipids containing mainly one fatty acid donor (N-linked palmitoyl-ceramide) in a fumonisin B1-independent manner. It uses palmitoyl-CoA as an acyl donor and is involved in the synthesis of C14, C16, and C18-ceramide.
LASS5 is the most abundantly expressed and predominant ceramide synthase isoform in lung epithelia. Recent studies show that LASS5 partially corrects growth and apoptosis.


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

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