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Thermo Fisher Scientific HADH Polyclonal Antibody
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Thermo Fisher Scientific HADH Polyclonal Antibody

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Thermo Fisher Scientific HADH Polyclonal Antibody는 인간, 마우스, 랫트에서 반응하는 Rabbit IgG 기반 항체입니다. Western blot, IHC, ICC/IF에 사용 가능하며, 항원 친화 크로마토그래피로 정제되었습니다. PBS/glycerol buffer에 보관하며 연구용으로 적합합니다.

카탈로그번호
PA531157
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 02:47
Thermo Fisher Scientific PA531157 HADH Polyclonal Antibody 100 ul pk판매 단위 pk ·
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657,900원VAT 포함 723,690원

Thermo Fisher Scientific · Thermo Fisher Scientific HADH Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution Publications
Western Blot (WB) 1:500–1:3,000 View 1 publication
Immunohistochemistry (Paraffin) (IHC (P)) 1:100–1:1,000 -
Immunocytochemistry (ICC/IF) 1:100–1:1,000 -

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Published Species Not Applicable
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fragment corresponding to a region within amino acids 92–314 of Human HADH (UniProt ID: Q16836-1)
Conjugate Unconjugated
Form Liquid
Concentration 0.49 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7, with 20% glycerol
Contains 0.025% ProClin 300
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_2548631

Product Specific Information

  • Recommended positive controls: 293T, A431, HeLa, HepG2, mouse liver, rat heart, rat liver
  • Predicted reactivity: Mouse (90%), Rat (91%), Xenopus laevis (85%), Pig (92%), Chicken (81%), Rhesus Monkey (96%), Bovine (90%)
  • Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

Target Information

This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene of this gene on chromosome 15.

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

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