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Thermo Fisher Scientific Spectrin alpha-1 Monoclonal Antibody (17C7)
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Thermo Fisher Scientific Spectrin alpha-1 Monoclonal Antibody (17C7)

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Spectrin alpha-1 단백질을 검출하는 Thermo Fisher Scientific의 17C7 모노클로날 항체입니다. Western blot, IHC, ICC/IF, ELISA 등 다양한 응용에 적합하며, 마우스 IgG1 형식의 액상 비결합 항체입니다. 연구용으로만 사용됩니다.

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마지막 업데이트 2025. 08. 01. 오후 12:08
Thermo Fisher Scientific MA191738 Spectrin alpha-1 Monoclonal Antibody (17C7) 100 ul pk판매 단위 pk ·
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834,900원VAT 포함 918,390원

Thermo Fisher Scientific · Thermo Fisher Scientific Spectrin alpha-1 Monoclonal Antibody (17C7)

Thermo Fisher Scientific Spectrin alpha-1 Monoclonal Antibody (17C7)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:100–1:1,000
Immunohistochemistry (Frozen) (IHC (F)) 1:10–1:50
Immunocytochemistry (ICC/IF) 1:100–1:500
ELISA 1:100,000–1:1,000,000

Product Specifications

Specification Description
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone 17C7
Immunogen Recombinant alpha I spectrin (erythroid spectrin) SH3 domain
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2194331

Product Specific Information

MA1-91738 detects alpha 1 Spectrin from mouse, rat, and human samples.
It has been successfully used in immunofluorescence, immunohistochemistry (frozen tissue), and Western blot applications.
The immunogen is recombinant alpha I spectrin (erythroid spectrin) SH3 domain.

Target Information

Spectrin is an actin crosslinking and molecular scaffold protein that links the plasma membrane to the actin cytoskeleton. It functions in determining cell shape, arrangement of transmembrane proteins, and organization of organelles.
Spectrin is a tetramer made up of alpha-beta dimers linked in a head-to-head arrangement. The encoded protein contains 22 spectrin repeats involved in dimer formation and forms weaker tetramer interactions than non-erythrocytic alpha spectrin, increasing plasma membrane elasticity and deformability of red blood cells.
Mutations in this gene are associated with hereditary red blood cell disorders such as elliptocytosis type 2, pyropoikilocytosis, and spherocytic hemolytic anemia.
(Information provided by RefSeq, Jul 2008)

Notice

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

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