Lipoamide Dehydrogenase (DLD) Mouse Monoclonal Antibody [Clone ID: OTI6D5]

CAT#: TA503387

DLD (Lipoamide Dehydrogenase) mouse monoclonal antibody, clone OTI6D5 (formerly 6D5)

Size: 30 ul 100 ul

Formulation: Standard Carrier-Free

Conjugation: Unconjugated Biotin HRP



  View other "OTI6D5" antibodies (4)

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参与“2024逐梦开学季·科研添动力”活动,可提供10 µL试用规格

CNY 1,999.00

CNY 2,700.00


货期*
现货

规格
    • 100 ul

经常一起买 (4)
Transient overexpression lysate of dihydrolipoamide dehydrogenase (DLD)
    • 100 ug

CNY 3,080.00


beta Actin Mouse Monoclonal Antibody, Clone OTI1, Loading Control
    • 30 ul

CNY 300.00
CNY 1,430.00


Recombinant protein of human dihydrolipoamide dehydrogenase (DLD), 20 µg
    • 20 ug

CNY 2,900.00
CNY 6,650.00


Recombinant protein of human dihydrolipoamide dehydrogenase (DLD), 100 µg
    • 100 ug

CNY 9,998.00

Specifications

Product Data
Clone Name OTI6D5
Applications FC, IF, IHC, WB
Recommend Dilution WB 1:2000, IHC 1:150, IF 1:100, FLOW 1:100
Reactivity Human, Mouse, Rat
Host Mouse
Clonality Monoclonal
Immunogen Full length human recombinant protein of human DLD(NP_000099) produced in HEK293T cell.
Formulation PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Concentration 0.82 mg/ml
Purification Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
Conjugation Unconjugated
Storage Condition Store at -20°C as received.
Predicted Protein Size 50.1 kDa
Gene Name dihydrolipoamide dehydrogenase
Background This gene encodes the L protein of the mitochondrial glycine cleavage system. The L protein, also named dihydrolipoamide dehydrogenase, is also a component of the pyruvate dehydrogenase complex, the alpha-ketoglutarate dehydrogenase complex, and the branched-chain alpha-keto acide dehydrogenase complex. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency. [provided by RefSeq]
Synonyms DLDD; DLDH; E3; GCSL; LAD; PHE3
Reference Data
Protein Families Druggable Genome
Protein Pathways Citrate cycle (TCA cycle), Glycine, serine and threonine metabolism, Glycolysis / Gluconeogenesis, Metabolic pathways, Pyruvate metabolism, Valine, leucine and isoleucine degradation
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

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