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Thermo Fisher Scientific A20A3 Polyclonal Antibody
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Thermo Fisher Scientific A20A3 Polyclonal Antibody

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ANKRD20A3 단백질을 인식하는 Rabbit Polyclonal Antibody로, WB, IHC, ICC 등 다양한 응용에 사용 가능. Human, Mouse, Rat 반응성. Affinity chromatography로 정제된 1 mg/mL 액상 형태. PBS buffer(50% glycerol) 보존, -20°C 보관.

카탈로그번호
PA599583
판매단위
pk
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마지막 업데이트 2025. 08. 03. 오전 04:44
Thermo Fisher Scientific PA599583 A20A3 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
764,500원VAT 포함 840,950원

Thermo Fisher Scientific · Thermo Fisher Scientific A20A3 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:1,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
Immunocytochemistry (ICC/IF) 1:100–1:500

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen A synthesized peptide derived from human ANKRD20A3 (Accession Q5VUR7), corresponding to amino acid residues A554–A604
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Affinity chromatography
Storage buffer PBS, pH 7.4, with 50% glycerol
Contains 0.02% sodium azide
Storage conditions -20°C
Shipping conditions Wet ice
RRID AB_2818516

Product Specific Information

Antibody detects endogenous levels of total ANKRD20.

Target Information

Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis.
ANKRD20A (ankyrin repeat domain-containing protein 20A) is an 823 amino acid protein that contains five ANK repeats. The gene encoding ANKRD20A maps to chromosome 9, which consists of about 145 million bases and encodes nearly 900 genes.
Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype.
Hereditary hemorrhagic telangiectasia, characterized by harmful vascular defects, and familial dysautonomia are associated with chromosome 9. Also, chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.


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

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