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Mouse Monoclonal PEPCK antibody (STJ98530)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB
Recommended dilution: WB 1:1000-1:2000
Recommended protocols: check protocols
Click or hover above images to see image description for PEPCK Monoclonal Antibody.
Check alternative names for the antibodyExpand
PCK2 antibody, PEPCK2 antibody,|EC 126.96.36.199 antibody|GTP mitochondrial precursor antibody|HGNC:8725 antibody|mitochondrial antibody|Mitochondrial phosphoenolpyruvate carboxykinase 2 antibody|OTTHUMP00000164700 antibody|PCK2 antibody|PCKGM_HUMAN antibody|PE antibody|PEP carboxykinase antibody|PEPCK antibody|PEPCK deficiency mitochondrial antibody|PEPCK M antibody|PEPCK-M antibody|PEPCK2 antibody|Phosphoenolpyruvate carboxykinase [GTP] antibody|Phosphoenolpyruvate carboxykinase 2 (mitochondrial) antibody|Phosphoenolpyruvate carboxykinase 2 mitochondrial antibody|Phosphoenolpyruvate carboxylase antibody|Phosphopyruvate carboxylase antibody|Anti-PCK2 antibody (ab70359)
SCBT cat No: sc-271204|sc-166778|sc-271029|sc-32879|sc-28477|sc-373972|
PEPCK Monoclonal Antibody
|Catalogue No.|| |
Human, Mouse, Rat, Cow, Dog, Pig
PEPCK Monoclonal Antibody detects endogenous levels of PEPCK protein.
Purified recombinant human PEPCK (C-terminus) protein fragments expressed in Ecoli
|Recommended dilution|| |
PEPCK Antibody was tube-contained. Purified in buffer containing 0.1M Tris-Glycine (pH 7.4, 150 mM NaCl) with 0.2% sodium azide, 50% glycerol.
PEPCK Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Phosphoenolpyruvate carboxykinase , mitochondrial antibody, PEPCK-M antibody,
|Protein names|| |
Phosphoenolpyruvate carboxykinase , mitochondrial , PEPCK-M ,
|Protein function|| |
Catalyzes the conversion of oxaloacetate (OAA) to phosphoenolpyruvate (PEP), the rate-limiting step in the metabolic pathway that produces glucose from lactate and other precursors derived from the citric acid cycle. / GTP + oxaloacetate = GDP + phosphoenolpyruvate + CO2. / Mn2+ /
|Involvement in disease|| |
Mitochondrial phosphoenolpyruvate carboxykinase deficiency (M-PEPCKD) [MIM:261650]: Metabolic disorder resulting from impaired gluconeogenesis. It is a rare disease with less than 10 cases reported in the literature. Clinical characteristics include hypotonia, hepatomegaly, failure to thrive, lactic acidosis and hypoglycemia. Autopsy reveals fatty infiltration of both the liver and kidneys. The disorder is transmitted as an autosomal recessive trait. Note: The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the phosphoenolpyruvate carboxykinase [GTP] family.
|Protein cellular localization|| |
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St John’s Laboratory Ltd.
|Product type|| |
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