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Thermo Fisher Scientific beta Galactosidase Polyclonal Antibody
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Thermo Fisher Scientific beta Galactosidase Polyclonal Antibody

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Beta Galactosidase 단백질을 인식하는 Rabbit Polyclonal 항체로, WB, IHC, ELISA, IP에 사용 가능. E.coli 유래 항원으로 제작되었으며, 비결합형(Unconjugated) 상태. 단기 보관은 4°C, 장기 보관은 -20°C 권장. 연구용 전용 제품.

카탈로그번호
100-4136
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 12:52
Thermo Fisher Scientific 100-4136 beta Galactosidase Polyclonal Antibody 2 mL pk판매 단위 pk ·
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420,400원VAT 포함 462,440원

Thermo Fisher Scientific · Thermo Fisher Scientific beta Galactosidase Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (IHC) 1:500
ELISA 1:65,000
Immunoprecipitation (IP) 1:500–1:2,000

Product Specifications

Specification Description
Species Reactivity Bacteria
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Beta Galactosidase (E. coli)
Conjugate Unconjugated
Form Lyophilized
Concentration 85 mg/mL
Storage Buffer 0.02 M potassium phosphate/whole serum, pH 7.2, with 0.15 M NaCl
Contains 0.01% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Store vial at 4°C prior to restoration. For extended storage, aliquot contents and freeze at -20°C or below. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4°C as an undiluted liquid. Dilute only prior to immediate use.

Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-rabbit serum, purified and partially purified Beta Galactosidase (E. coli). Cross-reactivity against Beta Galactosidase from other sources may occur but has not been specifically determined.

Target Information

Beta Galactosidase encodes a member of the glycosyl hydrolase 35 family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature lysosomal enzyme. This enzyme catalyzes the hydrolysis of a terminal beta-linked galactose residue from ganglioside substrates and other glycoconjugates. Mutations in this gene have been associated with GM1-gangliosidosis and Morquio B syndrome. Diseases associated with GLB1 include GM1-Gangliosidosis, Type I and Type II.


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

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