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Thermo Fisher Scientific FOLH1 Monoclonal Antibody (UMAB25), UltraMAB
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Thermo Fisher Scientific FOLH1 Monoclonal Antibody (UMAB25), UltraMAB

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FOLH1(PSMA) 단백질을 인식하는 UMAB25 단클론 항체로 Western blot, ICC/IF, ChIP assay에 사용 가능. 인간, 마우스, 랫, 개 시료 반응성. HEK293T 세포에서 발현된 전체 길이 인간 FOLH1 항원을 면역원으로 사용. 액상 형태로 제공되며 -20°C에서 보관.

카탈로그번호
UM570025
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오전 03:04
Thermo Fisher Scientific UM570025 FOLH1 Monoclonal Antibody (UMAB25), UltraMAB 30 ul pk판매 단위 pk ·
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301,100원VAT 포함 331,210원

Thermo Fisher Scientific · Thermo Fisher Scientific FOLH1 Monoclonal Antibody (UMAB25), UltraMAB

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunocytochemistry (ICC/IF) 1:100
ChIP assay (ChIP) Assay-dependent

Product Specifications

항목 내용
Species Reactivity Dog, Human, Mouse, Rat
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Clone UMAB25
Immunogen Full length human recombinant protein of human FOLH1 produced in HEK293T cell
Conjugate Unconjugated
Form Liquid
Concentration 0.5–1.0 mg/mL
Purification Affinity chromatography
Storage buffer PBS with 1% BSA, 50% glycerol
Contains 0.02% sodium azide
Storage conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping conditions Ambient (domestic); Wet ice (international)

Target Information

This gene encodes a type II transmembrane glycoprotein belonging to the M28 peptidase family. The protein acts as a glutamate carboxypeptidase on different alternative substrates, including the nutrient folate and the neuropeptide N-acetyl-L-aspartyl-L-glutamate. It is expressed in tissues such as the prostate, central and peripheral nervous system, and kidney. Mutations in this gene may lead to impaired intestinal absorption of dietary folates, resulting in low blood folate and hyperhomocysteinemia. Expression in the brain may be associated with pathological conditions linked to glutamate excitotoxicity. In the prostate, the protein is up-regulated in cancerous cells and serves as an effective diagnostic and prognostic indicator of prostate cancer. This gene likely arose from a duplication event of a nearby chromosomal region, and alternative splicing gives rise to multiple transcript variants encoding several isoforms.


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

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