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Thermo Fisher Scientific ABHD3 Polyclonal Antibody
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Thermo Fisher Scientific ABHD3 Polyclonal Antibody

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ABHD3 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody. 인간, 마우스, 랫트에 반응하며 IHC, ICC/IF, ELISA 등 다양한 응용 가능. 고순도 Protein A 정제, 안정적인 액상 형태로 연구용에 최적화.

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pk
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Thermo Fisher Scientific BS-7947R ABHD3 Polyclonal Antibody 100 ul pk판매 단위 pk
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531,800원VAT 포함 584,980원

Thermo Fisher Scientific · Thermo Fisher Scientific ABHD3 Polyclonal Antibody

Applications

Application Tested Dilution
Immunohistochemistry (Paraffin) (IHC (P)) Assay-dependent
Immunohistochemistry (Frozen) (IHC (F)) 1:100–1:500
Immunocytochemistry (ICC/IF) 1:50–1:200
ELISA 1:500–1:1,000

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen KLH conjugated synthetic peptide derived from human ABHD3, amino acids 201–285
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
Storage Buffer 0.01M TBS, pH 7.4, with 1% BSA, 50% glycerol
Contains 0.02% ProClin 300
Storage Conditions -20°C
Shipping Conditions Ambient (domestic); Wet ice (international)

Target Information

The α/β hydrolase superfamily comprises diverse members involved in important biochemical processes and various diseases. Despite differing sequences and substrates, they share a canonical α/β hydrolase fold with an eight-stranded parallel α/β structure and a catalytic triad (histidine, acid, nucleophile). Members of this superfamily are often drug targets for diseases such as diabetes, Alzheimer’s disease, obesity, and blood clotting disorders.

The α/β hydrolase domain containing (ABHD) gene subfamily includes 15 mostly uncharacterized members, most of which utilize a serine nucleophile to form the G-X-S-X-G nucleophile elbow.

  • ABHD1 plays a role in metabolizing smoking xenobiotics.
  • ABHD2 participates in the development of atherosclerosis.
  • ABHD3 is a 409 amino acid single-pass type II membrane protein.
  • ABHD4 is involved in an alternative synthesis pathway of NAE (N-acyl ethanolamine).
  • ABHD5 mutations contribute to Chanarin-Dorfman syndrome.
  • ABDH6 may play a role in nervous system metabolism and signaling.

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

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