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Thermo Fisher Scientific A20A1 Polyclonal Antibody
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Thermo Fisher Scientific A20A1 Polyclonal Antibody

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Rabbit polyclonal antibody against Human A20A1, validated for Western blot. Affinity-purified with >95% purity. Supplied as liquid in PBS with 50% glycerol. Suitable for Human, Mouse, Rat samples. For research use only.

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pk
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마지막 업데이트 2025. 08. 05. 오전 10:23
Thermo Fisher Scientific PA575795 A20A1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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642,300원VAT 포함 706,530원

Thermo Fisher Scientific · Thermo Fisher Scientific A20A1 Polyclonal Antibody

Applications

  • Western Blot (WB): 1:500–1:1,000

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to residues in Human A20A1
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 50% glycerol
Contains 0.02% sodium azide
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_2719523

Product Specific Information

The antibody was affinity-purified from rabbit antiserum by affinity chromatography using an epitope-specific immunogen. The purity is greater than 95% as determined by SDS-PAGE.

Target Information

Ankyrins are membrane adaptor molecules that play key roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations in ankyrin genes can cause severe genetic disorders such as fatal cardiac arrhythmias and hereditary spherocytosis.

ANKRD20A (ankyrin repeat domain-containing protein 20A) is an 823 amino acid protein containing five ANK repeats. The gene encoding ANKRD20A is located on chromosome 9, which spans approximately 145 million bases and encodes nearly 900 genes. This gene may be involved in gender determination, as deletion of the distal portion of 9p can lead to male-to-female sex reversal in individuals with an X,Y genotype.

Additionally, chromosome 9 is associated with disorders such as hereditary hemorrhagic telangiectasia and familial dysautonomia, and participates in the translocation with chromosome 22 that produces the BCR-ABL fusion protein found in certain leukemias.


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

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