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CPS1/Carbamoyl-Phosphate Synthetase (Hepatocellular Marker) Monoclonal Antibody (SPM615)

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Datasheet
Protocols
Questions & Answers

Cite CPS1/Carbamoyl-Phosphate Synthetase (Hepatocellular Marker) Monoclonal Antibody (SPM615)

  • Antibody Testing Data (1)
CPS1/Carbamoyl-Phosphate Synthetase (Hepatocellular Marker) Antibody in Immunohistochemistry (Paraffin) (IHC (P))
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CPS1/Carbamoyl-Phosphate Synthetase (Hepatocellular Marker) Antibody in Immunohistochemistry (Paraffin) (IHC (P))
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CPS1/Carbamoyl-Phosphate Synthetase (Hepatocellular Marker) Antibody (1373-MSM1X-P0) in IHC (P)

Formalin-fixed, paraffin-embedded human Hepatocellular Ca stained with CPS1 Monoclonal Antibody (SPM615). {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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CPS1/Carbamoyl-Phosphate Synthetase (Hepatocellular Marker) Antibody in Immunohistochemistry (Paraffin) (IHC (P))

Product Details

1373-MSM1X-P0

Applications
Tested Dilution
Publications

Immunohistochemistry (Paraffin) (IHC (P))

Assay-dependent
-

Immunohistochemistry (PFA fixed) (IHC (PFA))

1-2 µg/mL
-

Immunocytochemistry (ICC/IF)

2-4 µg/mL
-
Product Specifications

Species Reactivity

Dog, Human

Host/Isotype

Mouse / IgG1, kappa

Class

Monoclonal

Type

Antibody

Clone

SPM615

Immunogen

Recombinant human CPS1 protein

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

200 µg/mL

Purification

Protein A/G

Storage buffer

PBS, pH 7.4, with 0.05% BSA

Contains

0.05% sodium azide

Storage conditions

4°C, do not freeze

Shipping conditions

Wet ice

Target Information

The mitochondrial enzyme encoded by this gene catalyzes synthesis of carbamoyl phosphate from ammonia and bicarbonate. This reaction is the first committed step of the urea cycle, which is important in the removal of excess urea from cells. The encoded protein may also represent a core mitochondrial nucleoid protein. Three transcript variants encoding different isoforms have been found for this gene. The shortest isoform may not be localized to the mitochondrion. Mutations in this gene have been associated with carbamoyl phosphate synthetase deficiency, susceptibility to persistent pulmonary hypertension, and susceptibility to venoocclusive disease after bone marrow transplantation.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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Bioinformatics

Protein Aliases: carbamoyl-phosphate synthase (ammonia); carbamoyl-phosphate synthase 1, mitochondrial; Carbamoyl-phosphate synthase [ammonia], mitochondrial; carbamoyl-phosphate synthetase 1, mitochondrial; Carbamoyl-phosphate synthetase I; carbamoylphosphate synthetase I; CPSase I

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Gene Aliases: CPS1; CPSASE1; PHN

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UniProt ID: (Human) P31327

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Entrez Gene ID: (Human) 1373, (Dog) 488506

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Function(s)
aspartate carbamoyltransferase activity carbamoyl-phosphate synthase (ammonia) activity carbamoyl-phosphate synthase (glutamine-hydrolyzing) activity dihydroorotase activity endopeptidase activity calcium ion binding protein binding ATP binding phospholipid binding glutamate binding protein complex binding modified amino acid binding
Process(es)
urea cycle glycogen catabolic process 'de novo' pyrimidine nucleobase biosynthetic process proteolysis arginine biosynthetic process glutamine metabolic process midgut development response to toxic substance response to zinc ion response to amine citrulline biosynthetic process triglyceride catabolic process response to food response to lipopolysaccharide response to drug response to starvation response to amino acid cellular response to fibroblast growth factor stimulus positive regulation of vasodilation nitric oxide metabolic process homocysteine metabolic process anion homeostasis response to growth hormone hepatocyte differentiation carbamoyl phosphate biosynthetic process cellular response to cAMP cellular response to glucagon stimulus cellular response to oleic acid response to dexamethasone
It has to be done as per old AB suggested Products section.
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