Rabbit Anti-GLUD1 Recombinant Antibody (G3910) (V2LY-1225-LY1545)

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Basic Information

Host Animal
Rabbit
Clone
G3910
Application
WB, IHC, IF, FC
Immunogen
Human GLUD1.
Host Species
Rabbit
Specificity
Human, Mouse, Rat
Antibody Isotype
IgG
Clonality
Monoclonal
Application Notes
ApplicationNote
WB1:1,000-1:2,000
IF(ICC)1:50-1:200
IHC1:100-1:200
FC1:20-1:100

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
PBS, BSA, glycerol
Preservative
Sodium azide
Concentration
1 mg/ml
Purity
> 95% Purity determined by SDS-PAGE.
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.
More Infomation

Target

Full Name
Glutamate Dehydrogenase 1
Entrez Gene ID
Human2746
Mouse14661
Rat24399
UniProt ID
HumanP00367
MouseP26443
RatP10860
Function
Mitochondrial glutamate dehydrogenase that catalyzes the conversion of L-glutamate into alpha-ketoglutarate. Plays a key role in glutamine anaplerosis by producing alpha-ketoglutarate, an important intermediate in the tricarboxylic acid cycle (PubMed:11032875, PubMed:16959573, PubMed:11254391, PubMed:16023112).

Plays a role in insulin homeostasis (PubMed:9571255, PubMed:11297618).

May be involved in learning and memory reactions by increasing the turnover of the excitatory neurotransmitter glutamate (By similarity).
Biological Process
Glutamate biosynthetic process Source: BHF-UCL
Glutamate catabolic process Source: UniProtKB
Glutamine metabolic process Source: UniProtKB
Positive regulation of insulin secretion Source: BHF-UCL
Substantia nigra development Source: UniProtKB
Tricarboxylic acid metabolic process Source: UniProtKB
Cellular Location
Endoplasmic reticulum; Mitochondrion. Mostly translocates into the mitochondria, only a small amount of the protein localizes to the endoplasmic reticulum.
Involvement in disease
Familial hyperinsulinemic hypoglycemia 6 (HHF6):
Familial hyperinsulinemic hypoglycemia [MIM:256450], also referred to as congenital hyperinsulinism, nesidioblastosis, or persistent hyperinsulinemic hypoglycemia of infancy (PPHI), is the most common cause of persistent hypoglycemia in infancy and is due to defective negative feedback regulation of insulin secretion by low glucose levels. In HHF6 elevated oxidation rate of glutamate to alpha-ketoglutarate stimulates insulin secretion in the pancreatic beta cells, while they impair detoxification of ammonium in the liver.
PTM
ADP-ribosylated by SIRT4, leading to inactivate glutamate dehydrogenase activity (PubMed:16959573). Stoichiometry shows that ADP-ribosylation occurs in one subunit per catalytically active homohexamer (PubMed:16023112).
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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