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Anti-D2HGDH Antibody (aa332-381) LS-C169795

Ordering

Wt. Vol. Conc. Price
50 µg 50 µl 1 mg/ml $365
Inquire for larger quantities

LSBio (Direct) LSBio (Direct)
206-374-1102
866-206-6909
Orders@LSBio.com
 

Most Popular D2HGDH Antibodies

Anti-D2HGDH Antibody (aa332-381) LS-C169795
Rabbit Polyclonal to Human D2HGDH
Human, Mouse, Rabbit
Western blot
Unconjugated
Western blot Image
Anti-D2HGDH Antibody (aa69-118) LS-C186811
Rabbit Polyclonal to Human D2HGDH
Human
Western blot
Unconjugated
Western blot Image
Anti-D2HGDH Antibody LS-C333943
Rabbit Polyclonal (IgG) to Human D2HGDH
Human, Mouse, Rat
Western blot
Unconjugated

100% Guaranteed 100% Guaranteed
Rabbit Polyclonal to Human D2HGDH
Human, Mouse, Rabbit
Western blot (applications tested for the base form of this product only)
Unconjugated

Details

Human D2HGDH
Rabbit
Human, Mouse, Rabbit (tested or 100% immunogen sequence identity)
Monkey, Rat (at least 90% immunogen sequence identity)
Polyclonal
Unconjugated. Also available conjugated with Biotin, FITC, HRP.
Immunoaffinity purified
Unmodified

Applications

  • Western blot
  • (applications tested for the base form of this product only)

Specificity and Use

D2HGDH antibody was raised against synthetic peptide located between aa332-381 of human D2HGDH (Q8N465, NP_689996). Percent identity by BLAST analysis: Human, Chimpanzee, Gorilla, Gibbon, Marmoset, Mouse, Rabbit (100%); Orangutan, Monkey, Rat (92%); Horse (85%).
LS-E24160 - Lyophilized - 100 µg - $145.00
aa332-381
Human D2HGDH

Packaging

Lyophilized from PBS
50 µl Distilled water
Long term: -20°C, the use of 50% glycerol is recommended if storing aliquots in -20°C for long term use (up to 1 year); Short term (less than one week): +4°C. Avoid repeat freeze-thaw cycles.
For research use only.

About D2HGDH

Q8N465 Q8N465

D2HGDH Antibody, D2HGD Antibody

D2HGDH is D-2hydroxyglutarate dehydrogenase, a mitochondrial enzyme belonging to the FAD-binding oxidoreductase/transferase type 4 family. This enzyme, which is most active in liver and kidney but also active in heart and brain, converts D-2-hydroxyglutarate to 2-ketoglutarate. Mutations in this gene are present in D-2-hydroxyglutaric aciduria, a rare recessive neurometabolic disorder causing developmental delay, epilepsy, hypotonia, and dysmorphic features.

Western blot

Western blot
This image was taken for the unconjugated form of this product. Other forms have not been tested.
 

Requested From: United States
Date Requested: 12/10/2016

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