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Thermo Fisher Scientific ACY1 Polyclonal Antibody, MaxPab
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Thermo Fisher Scientific ACY1 Polyclonal Antibody, MaxPab

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Thermo Fisher Scientific의 ACY1 Polyclonal Antibody는 인간 및 마우스 시료에서 Western blot에 적합한 토끼 유래 다클론 항체입니다. ACY1 전장 단백질(1–408 a.a.)을 면역원으로 사용했으며, PBS(pH 7.4) 용액 형태로 제공됩니다. 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 05. 오후 07:06
Thermo Fisher Scientific H00000095-D01P ACY1 Polyclonal Antibody, MaxPab 100 ug pk판매 단위 pk ·
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582,600원VAT 포함 640,860원

Thermo Fisher Scientific · Thermo Fisher Scientific ACY1 Polyclonal Antibody, MaxPab

Applications

  • Western Blot (WB): 1:500–1:1,000

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen ACY1 (NP_000657.1, 1–408 a.a.) full-length human protein
Conjugate Unconjugated
Form Liquid
Concentration See Label
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4
Contains No preservative
Storage Conditions -20 °C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Sequence of this protein is as follows:
MTSKGPEEEH PSVTLFRQYL RIRTVQPKPD YGAAVAFFEE TARQLGLGCQ KVEVAPGYVV TVLTWPGTNP TLSSILLNSH TDVVPVFKEH WSHDPFEAFK DSEGYIYARG AQDMKCVSIQ YLEAVRRLKV EGHRFPRTIH MTFVPDEEVG GHQGMELFVQ RPEFHALRAG FALDEGIANP TDAFTVFYSE RSPWWVRVTS TGRPGHASRF MEDTAAEKLH KVVNSILAFR EKEWQRLQSN PHLKEGSVTS VNLTKLEGGV AYNVIPATMS ASFDFRVAPD VDFKAFEEQL QSWCQAAGEG VTLEFAQKWM HPQVTPTDDS NPWWAAFSRV CKDMNLTLEP EIMPAATDNR YIRAVGVPAL GFSPMNRTPV LLHDHDERLH EAVFLRGVDI YTRLLPALAS VPALPSDS

Target Information

ACY1 encodes a cytosolic, homodimeric, zinc-binding enzyme that catalyzes the hydrolysis of acylated L-amino acids to L-amino acids and an acyl group. It is implicated in the catabolism and salvage of acylated amino acids. The gene is located on chromosome 3p21.1, a region often reduced to homozygosity in small-cell lung cancer (SCLC), where its expression may be reduced or undetectable. Mutations in this gene cause aminoacylase-1 deficiency, a metabolic disorder characterized by CNS defects and increased urinary excretion of N-acetylated amino acids. Alternative splicing results in multiple transcript variants, and a related pseudogene exists on chromosome 18.


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

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