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Thermo Fisher Scientific SLC52A2 Polyclonal Antibody
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Thermo Fisher Scientific SLC52A2 Polyclonal Antibody

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Human SLC52A2 단백질에 특이적인 Rabbit polyclonal antibody로, IHC(P) 등 다양한 연구용 응용에 적합. 항원 친화 크로마토그래피로 정제되었으며, 액상 형태로 제공. 뇌 조직에서 높은 발현을 보이는 리보플라빈 수송체 연구에 활용 가능.

카탈로그번호
PA564086
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 11:37
Thermo Fisher Scientific PA564086 SLC52A2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific SLC52A2 Polyclonal Antibody

Applications

  • Immunohistochemistry (Paraffin) (IHC (P)): 1:50–1:200

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human SLC52A2. Recombinant protein control fragment (Product #RP-104034).
Conjugate Unconjugated
Form Liquid
Concentration 0.2 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% 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_2647536

Product Specific Information

  • Immunogen sequence: ELGSGLQVGA PGAEEEVEES SPL
  • Highest antigen sequence identity to orthologs:
    • Mouse: 57%
    • Rat: 56%

Target Information

This gene encodes a membrane protein belonging to the riboflavin transporter family. Riboflavin must be obtained by intestinal absorption as it cannot be synthesized by the body. The water-soluble vitamin riboflavin is processed into coenzymes FMN and FAD, which act as intermediaries in many cellular metabolic reactions.
Paralogous members of this gene family are located on chromosomes 17 and 20. This gene shows higher expression in brain tissue than in the small intestine.
Alternative splicing results in multiple transcript variants encoding the same protein. Mutations in this gene have been associated with Brown-Vialetto-Van Laere syndrome 2, an autosomal recessive progressive neurologic disorder characterized by deafness, bulbar dysfunction, and axial and limb hypotonia.
[provided by RefSeq, Jul 2012]


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

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