PGD anticorps (AA 184-483)
Aperçu rapide pour PGD anticorps (AA 184-483) (ABIN6145502)
Antigène
Voir toutes PGD AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 184-483
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Séquence
- KMVHNGIEYG DMQLICEAYH LMKDVLGMAQ DEMAQAFEDW NKTELDSFLI EITANILKFQ DTDGKHLLPK IRDSAGQKGT GKWTAISALE YGVPVTLIGE AVFARCLSSL KDERIQASKK LKGPQKFQFD GDKKSFLEDI RKALYASKII SYAQGFMLLR QAATEFGWTL NYGGIALMWR GGCIIRSVFL GKIKDAFDRN PELQNLLLDD FFKSAVENCQ DSWRRAVSTG VQAGIPMPCF TTALSFYDGY RHEMLPASLI QAQRDYFGAH TYELLAKPGQ FIHTNWTGHG GTVSSSSYNA
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Réactivité croisée
- Humain, Souris, Rat
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Attributs du produit
- Polyclonal Antibodies
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Immunogène
- Recombinant fusion protein containing a sequence corresponding to amino acids 184-483 of human PGD (NP_002622.2).
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Isotype
- IgG
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Indications d'application
- WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200
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Commentaires
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HIGH QUALITY
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Restrictions
- For Research Use only
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Format
- Liquid
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Buffer
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- -20 °C
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Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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- PGD (Phosphogluconate Dehydrogenase (PGD))
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Autre désignation
- PGD
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Sujet
- 6-phosphogluconate dehydrogenase is the second dehydrogenase in the pentose phosphate shunt. Deficiency of this enzyme is generally asymptomatic, and the inheritance of this disorder is autosomal dominant. Hemolysis results from combined deficiency of 6-phosphogluconate dehydrogenase and 6-phosphogluconolactonase suggesting a synergism of the two enzymopathies. Several transcript variants encoding different isoforms have been found for this gene.,PGD,6PGD,Signal Transduction,Endocrine & Metabolism,PGD
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Poids moléculaire
- 51 kDa/53 kDa
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ID gène
- 5226
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UniProt
- P52209
Antigène
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