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Thermo Fisher Scientific RFTN1 Polyclonal Antibody
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Thermo Fisher Scientific RFTN1 Polyclonal Antibody

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RFTN1 단백질을 인식하는 Rabbit Polyclonal Antibody로 Western blot 및 ELISA에 적합. Human, Mouse, Rat 시료에 반응하며, 세포막 단백질 Raftlin 연구에 활용 가능. PBS/glycerol buffer로 안정화되어 -20°C 보관.

카탈로그번호
PA587893
판매단위
pk
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마지막 업데이트 2025. 08. 02. 오전 06:12
Thermo Fisher Scientific PA587893 RFTN1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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618,800원VAT 포함 680,680원

Thermo Fisher Scientific · Thermo Fisher Scientific RFTN1 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
ELISA 1 µg/mL

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fusion protein containing a sequence corresponding to amino acids 1–260 of human RFTN1 (NP_055965.1)
Conjugate Unconjugated
Form Liquid
Concentration 1.83 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2804485

Product Specific Information

Immunogen sequence:
MGCGLNKLEK RDEKRPGNIY STLKRPQVET KIDVSYEYRF LEFTTLSAAE LPGSSAVRLA SLRDLPAQLL ELYQQGFSLA ALHPFVQPTH EREKTPLEHI FRAILIKKTD RSQKTDLHNE GYILELDCCS SLDHPTDQKL IPEFIKKIQE AASQGLKFVG VIPQYHSSVN SAGSSAPVST ANSTEDARDA KNARGDHASL ENEKPGTGDV CSAPAGRNQS PEPSSGPRGE VPLAKQPSSP SGEGDGGELS PQGVSKTLDG

Positive Samples: A-549, Mouse liver
Cellular Location: Cell membrane, Lipid-anchor


Target Information

Raftlin (RFTN1, raftlin lipid raft linker 1) is a 578 amino acid cell membrane lipid-anchored protein essential for raft cell assembly and maintenance. It modulates B-cell antigen receptor-mediated signaling, TCR signals, and participates in T cell-mediated immune responses.
The RFTN1 gene is located on human chromosome 3, which contains over 1,100 genes including chemokine receptor clusters and tumor suppressor loci such as RASSF1, HYAL1, and SEMA3B.
Mutations in genes on chromosome 3 are associated with genetic diseases such as Marfan Syndrome, Porphyria, von Hippel-Lindau Syndrome, Osteogenesis Imperfecta, and Charcot-Marie-Tooth Disease.


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

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