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Thermo Fisher Scientific FOLH1/PSMA (Prostate Epithelial Marker) Monoclonal Antibody (FOLH1/2121)
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Thermo Fisher Scientific FOLH1/PSMA (Prostate Epithelial Marker) Monoclonal Antibody (FOLH1/2121)

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인체 PSMA(FOLH1) 단백질을 인식하는 Mouse monoclonal 항체로, ELISA 등 연구용에 적합합니다. Protein A/G로 정제된 액상 형태이며, 보존제 없이 PBS(pH 7.4)에 용해되어 있습니다. 전립선암 관련 연구 및 표지자 분석에 유용합니다.

카탈로그번호
2346-MSM1-P1ABX
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 05:02
Thermo Fisher Scientific 2346-MSM1-P1ABX FOLH1/PSMA (Prostate Epithelial Marker) Monoclonal Antibody (FOLH1/2121) 100 ug pk판매 단위 pk ·
재고 확인 필요
900,300원VAT 포함 990,330원

Thermo Fisher Scientific · Thermo Fisher Scientific FOLH1/PSMA (Prostate Epithelial Marker) Monoclonal Antibody (FOLH1/2121)

Applications

  • ELISA (ELISA): Assay-dependent

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2b, kappa
Class Monoclonal
Type Antibody
Clone FOLH1/2121
Immunogen Recombinant human FOLH1 protein fragment (around aa 232–433)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A/G
Storage Buffer PBS, pH 7.4
Contains No preservative
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, and is expressed in several tissues such as prostate, central and peripheral nervous system, and kidney.
A mutation in this gene may be associated with impaired intestinal absorption of dietary folates, resulting in low blood folate levels and consequent hyperhomocysteinemia. Expression in the brain may be involved in pathological conditions associated with glutamate excitotoxicity. In the prostate, the protein is upregulated 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. Alternative splicing gives rise to multiple transcript variants encoding several different isoforms.


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

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