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Thermo Fisher Scientific ALDOA Monoclonal Antibody (3D9-6F3)
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Thermo Fisher Scientific ALDOA Monoclonal Antibody (3D9-6F3)

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ALDOA 단백질을 인식하는 Thermo Fisher Scientific의 Mouse Monoclonal Antibody (Clone 3D9-6F3)로, Human 시료에 반응합니다. WB, ICC/IF, ELISA에 적합하며, 액상 형태로 제공됩니다. Affinity chromatography로 정제된 고품질 연구용 항체입니다.

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pk
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마지막 업데이트 2025. 08. 05. 오후 03:43
Thermo Fisher Scientific H00000226-M01 ALDOA Monoclonal Antibody (3D9-6F3) 100 ug pk판매 단위 pk ·
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518,100원VAT 포함 569,910원

Thermo Fisher Scientific · Thermo Fisher Scientific ALDOA Monoclonal Antibody (3D9-6F3)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1–5 µg/mL
Immunocytochemistry (ICC/IF) 10 µg/mL
ELISA 10 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2b, kappa
Class Monoclonal
Type Antibody
Clone 3D9-6F3
Immunogen ALDOA (AAH10660.1, 1–364 a.a.) full-length recombinant protein with GST tag (MW of GST tag: 26 kDa)
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:
MPYQYPALTP EQKKELSDIA HRIVAPGKGI LAADESTGSI AKRLQSIGTE NTEENRRFYR QLLLTADDRV NPCIGGVILF HETLYQKADD GRPFPQVIKS KGGVVGIKVD KGVVPLAGTN GETTTQGLDG LSERCAQYKK DGADFAKWRC VLKIGEHTPS ALAIMENANV LARYASICQQ NGIVPIVEPE ILPDGDHDLK RCQYVTEKVL AAVYKALSDH HIYLEGTLLK PNMVTPGHAC TQKFSHEEIA MATVTALRRT VPPAVTGITF LSGGQSEEEA SINLNAINKC PLLKPWALTF SYGRALQASA LKAWGGKKEN LKAAQEEYVK RALANSLACQ GKYTPSGQAG AAASESLFVS NHAY


Target Information

Aldolase encodes a member of the class I fructose-bisphosphate aldolase protein family. The encoded protein is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate.
Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development.
Mutations in this gene have been associated with Glycogen Storage Disease XII, an autosomal recessive disorder associated with hemolytic anemia.
Disruption of this gene also plays a role in the progression of multiple types of cancers. Related pseudogenes have been identified on chromosomes 3 and 10.


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

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