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Thermo Fisher Scientific Ferritin Light Chain Recombinant Rabbit Monoclonal Antibody (4T7Z7)
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Thermo Fisher Scientific Ferritin Light Chain Recombinant Rabbit Monoclonal Antibody (4T7Z7)

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Ferritin Light Chain을 인식하는 재조합 토끼 단클론 항체(4T7Z7). WB, IHC, ELISA에 사용 가능하며 인간, 마우스, 랫트 반응성. HEK293 세포에서 발현된 IgG 형식, 액상 형태로 제공. -20°C 보관, 연구용 전용.

카탈로그번호
MA535088
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 02:42
Thermo Fisher Scientific MA535088 Ferritin Light Chain Recombinant Rabbit Monoclonal Antibody (4T7Z7) 100 ul pk판매 단위 pk ·
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598,300원VAT 포함 658,130원

Thermo Fisher Scientific · Thermo Fisher Scientific Ferritin Light Chain Recombinant Rabbit Monoclonal Antibody (4T7Z7)

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:2,000–1:9,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:400–1:2,000
ELISA 1 µg/mL

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone 4T7Z7
Immunogen Recombinant fusion protein containing a sequence corresponding to amino acids 1–175 of human Ferritin Light Chain (NP_0001372)
Conjugate Unconjugated
Form Liquid
Concentration 0.55 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol, 0.05% BSA
Contains 0.05% ProClin 300
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2848993

Product Specific Information

Immunogen sequence:

MSSQIRQNYS TDVEAAVNSL VNLYLQASYT YLSLGFYFDR DDVALEGVSH FFRELAEEKR 
EGYERLLKMQ NQRGGRALFQ DIKKPAEDEW GKTPDAMKAA MALEKKLNQA LLDLHALGSA 
RTDPHLCDFL ETHFLDEEVK LIKKMGDHLT NLHRLGGPEA GLGEYLFERL TLKHD

Target Information

This gene encodes the light subunit of the ferritin protein. Ferritin is the major intracellular iron storage protein in prokaryotes and eukaryotes, composed of 24 subunits of heavy and light ferritin chains. Variation in subunit composition may affect iron uptake and release rates in tissues. A major function of ferritin is to store iron in a soluble and non-toxic form. Defects in this gene are associated with neurodegenerative diseases and hyperferritinemia-cataract syndrome. This gene has multiple pseudogenes.


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

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