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Thermo Fisher Scientific Aldolase A Polyclonal Antibody
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Thermo Fisher Scientific Aldolase A Polyclonal Antibody

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Aldolase A 단백질을 인식하는 Rabbit Polyclonal Antibody로, WB 및 IHC(P)에서 사용 가능. Human, Mouse, Rat에 반응하며 항원 친화 크로마토그래피로 정제됨. Recombinant protein 기반 면역원 사용, 연구용으로 적합.

카탈로그번호
PA577857
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 09:47
Thermo Fisher Scientific PA577857 Aldolase A Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
754,700원VAT 포함 830,170원

Thermo Fisher Scientific · Thermo Fisher Scientific Aldolase A Polyclonal Antibody

Applications

Application Tested Dilution Publications
Western Blot (WB) 1:500–1:3,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:100–1:1,000

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein encompassing a sequence within the center region of human Aldolase A. The exact sequence is proprietary.
Conjugate Unconjugated
Form Liquid
Concentration 0.58 mg/mL
Purification Antigen affinity chromatography
Storage buffer 0.1M Tris glycine, pH 7, with 20% glycerol
Contains 0.01% thimerosal
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_2735444

Product Specific Information

  • Positive Control: 293T, A431, HeLa, HepG2, mouse brain, rat brain
  • Predicted Reactivity: Japanese Medaka (83%), Xenopus laevis (86%), Rabbit (98%), Chimpanzee (100%), Bovine (98%)
  • Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

Target Information

Aldolase encodes a member of the class I fructose-bisphosphate aldolase protein family. The encoded protein is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate.
Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development.
Mutations in this gene have been associated with Glycogen Storage Disease XII, an autosomal recessive disorder associated with hemolytic anemia. Disruption of this gene also plays a role in the progression of multiple types of cancers. Related pseudogenes have been identified on chromosomes 3 and 10.

WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm.
For more information, visit www.P65Warnings.ca.gov.

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

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