ARG56303

anti-Lipoamide Dehydrogenase antibody

anti-Lipoamide Dehydrogenase antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Mouse

Overview

Product Description Rabbit Polyclonal antibody recognizes Lipoamide Dehydrogenase
Tested Reactivity Hu, Ms
Tested Application IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name Lipoamide Dehydrogenase
Antigen Species Human
Immunogen Recombinant protein of Human Lipoamide Dehydrogenase
Conjugation Un-conjugated
Alternate Names DLDH; LAD; Dihydrolipoamide dehydrogenase; DLDD; PHE3; EC 1.8.1.4; Glycine cleavage system L protein; Dihydrolipoyl dehydrogenase, mitochondrial; GCSL; E3

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P1:50 - 1:200
WB1:500 - 1:2000
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Positive Control BT474

Properties

Form Liquid
Purification Affinity purification with immunogen.
Buffer PBS (pH 7.3), 0.02% Sodium azide and 50% Glycerol.
Preservative 0.02% Sodium azide
Stabilizer 50% Glycerol
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 13382 Mouse DLD

GeneID: 1738 Human DLD

Swiss-port # O08749 Mouse Dihydrolipoyl dehydrogenase, mitochondrial

Swiss-port # P09622 Human Dihydrolipoyl dehydrogenase, mitochondrial

Gene Symbol DLD
Gene Full Name dihydrolipoamide dehydrogenase
Background This gene encodes a member of the class-I pyridine nucleotide-disulfide oxidoreductase family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. In homodimeric form, the encoded protein functions as a dehydrogenase and is found in several multi-enzyme complexes that regulate energy metabolism. However, as a monomer, this protein can function as a protease. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]
Function Lipoamide dehydrogenase is a component of the glycine cleavage system as well as of the alpha-ketoacid dehydrogenase complexes. Involved in the hyperactivation of spermatazoa during capacitation and in the spermatazoal acrosome reaction. [UniProt]
Calculated MW 54 kDa
PTM Tyrosine phosphorylated.

Images (2) Click the Picture to Zoom In

  • ARG56303 anti-Lipoamide Dehydrogenase antibody IHC-P image

    Immunohistochemistry: Paraffin-embedded Human liver injury stained with ARG56303 anti-Lipoamide Dehydrogenase antibody at 1:100 dilution.

  • ARG56303 anti-Lipoamide Dehydrogenase antibody WB image

    Western blot: BT474 cell lysate stained with ARG56303 anti-Lipoamide Dehydrogenase antibody.