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L2HGDH antibody (Middle Region)
L2HGDH
Reactivity: Human, Mouse
WB, EIA
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-L2HGDH Antibody
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Target
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L2HGDH
(L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))
Binding Specificity
All epitopes for L2HGDH antibodies
AA 139-167, Middle Region
Reactivity
All reactivities for L2HGDH antibodies
Human, Mouse
Host
All hosts for L2HGDH antibodies
Rabbit
Clonality
All clonalities for L2HGDH antibodies
Polyclonal
Conjugate
All conjugates for L2HGDH antibodies
This L2HGDH antibody is un-conjugated
Application
All applications for L2HGDH antibodies
Western Blotting (WB), Enzyme Immunoassay (EIA)
Specificity
This antibody detects L2HGDH/ Duranin.
Cross-Reactivity (Details)
Species reactivity (tested):Human, Mouse
Purification
Purified through a protein A column; followed by peptide affinity purification.
Immunogen
Synthetic peptide - KLH conjugated - corresponding to the central region (between 139-167aa) of human L2HGDH/Duranin.
Isotype
Ig Fraction
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Discover our top product L2HGDH Primary Antibody
Alternatives
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Application Details
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Application Notes
Optimal working dilution should be determined by the investigator.
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.25 mg/mL
Buffer
PBS with 0.09 % (W/V) Sodium Azide.
Preservative
Sodium azide
Precaution of Use
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Handling Advice
Avoid repeated freezing and thawing.
Storage
4 °C/-20 °C
Storage Comment
Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
Target Details for L2HGDH
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Target
L2HGDH
(L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))
Alternative Name
Duranin (L2HGDH Products )
Synonyms
RGD1306250 antibody, C14orf160 antibody, BC016226 antibody, L-2-hydroxyglutarate dehydrogenase antibody, L2hgdh antibody, L2HGDH antibody
Background
The L2HGDH gene encodes L-2-hydroxyglutarate dehydrogenase, a FAD-dependent enzyme that oxidizes L-2-hydroxyglutarate to alpha-ketoglutarate in a variety of mammalian tissues. Mutations in this gene cause L-2-hydroxyglutaric aciduria, a rare autosomal recessive neurometabolic disorder resulting in moderate to severe mental retardation.Synonyms: C14orf160, L-2-hydroxyglutarate dehydrogenase, L2HGDH, hydroxyglutarate dehydrogenase
Gene ID
79944
NCBI Accession
NP_079160
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