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Thermo Fisher Scientific Ataxin 7 Polyclonal Antibody
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Thermo Fisher Scientific Ataxin 7 Polyclonal Antibody

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Ataxin 7 단백질을 인식하는 Rabbit Polyclonal 항체로, Western blot 및 Immunohistochemistry에 적합합니다. Human 및 Fruit fly 등 다양한 종에 반응하며, 항원 친화 크로마토그래피로 정제되었습니다. -20°C에서 보관하며 연구용으로 사용됩니다.

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마지막 업데이트 2025. 08. 01. 오후 06:37
Thermo Fisher Scientific PA1749 Ataxin 7 Polyclonal Antibody 100 ug pk판매 단위 pk ·
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710,700원VAT 포함 781,770원

Thermo Fisher Scientific · Thermo Fisher Scientific Ataxin 7 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1 µg/mL View 11 publications
Immunohistochemistry (IHC) - View 5 publications
Immunohistochemistry (Frozen) (IHC (F)) Assay-dependent View 2 publications
Immunohistochemistry - Free Floating (IHC (Free)) - View 1 publication
Immunocytochemistry (ICC/IF) 2 µg/mL View 3 publications
Immunoprecipitation (IP) - View 2 publications

Product Specifications

항목 내용
Species Reactivity Fruit fly, Human
Published Species Fruit fly, Human, Mouse, Non-human primate, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic Peptide: M(1) S E R A A D D V R G E P R R A A(17) C
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS with 1 mg/mL BSA
Contains 0.05% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2061308

Product Specific Information

PA1-749 detects ataxin 7 protein from transfected cell lysate.
PA1-749 has been successfully used in immunohistochemistry and Western blot procedures.
By Western blot, this antibody detects an ~96 kDa protein representing human ataxin 7 in transfected COS-1 cells.
The immunizing peptide corresponds to amino acid residues 1–17 from human ataxin 7, which is completely conserved in mouse ataxin 7.
This peptide (Cat. # PEP-217) is available for use in neutralization and control experiments.


Target Information

Spinocerebellar ataxia type 7 (SCA7) is a hereditary neurodegenerative disease caused by expanded polyglutamine (CAG) repeats at the N-terminus.
This autosomal dominant cerebellar ataxia primarily affects the cerebellum, retina, and brain stem, leading to dementia and macular degeneration.
The SCA7 gene encodes an 892-residue protein, ataxin-7, typically located in the cytoplasm and nuclear membrane of normal brain neurons.
Mutations in SCA7 cause ataxin 7 accumulation in intranuclear inclusions, resulting in cell death.


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

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