AQPEP (C-Term) RB52724 polyclonal, anti-human
€144.00
In stock
SKU
AC-AP21461b
Catalog Number: AC-AP21461b
Size: 80 µl
Other Size: 80 µl
Host: Rabbit Ig
Applications: WB
Datasheet
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Size: 80 µl
Other Size: 80 µl
Host: Rabbit Ig
Applications: WB
Datasheet
Request Information
Background:
Metalloprotease which may be important for placentation by regulating biological activity of key peptides at the embryo- maternal interface. On synthetic substrates it shows a marked preference for Leu-4-methylcoumaryl-7-amide (Leu-MCA) over Met- MCA, Arg-LCA and Lys-LCA. Cleaves the N-terminal amino acid of several peptides such as angiotensin-3, kisspeptin-10 and endokinin C.
Other Names: Aminopeptidase Q, AP-Q, 3411-, CHL2 antigen, Laeverin, AQPEP, LVRN
Target/Specificity:
This AQPEP antibody is generated from a rabbit immunized with a KLH conjugated synthetic peptide between 844-877 amino acids from human AQPEP.
Dilution: 1:2000
Calculated MW: 113283
Gene Name: LVRN (HGNC:26904)
Gene ID: 206338
Primary Accession: Q6Q4G3
Format: Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
Metalloprotease which may be important for placentation by regulating biological activity of key peptides at the embryo- maternal interface. On synthetic substrates it shows a marked preference for Leu-4-methylcoumaryl-7-amide (Leu-MCA) over Met- MCA, Arg-LCA and Lys-LCA. Cleaves the N-terminal amino acid of several peptides such as angiotensin-3, kisspeptin-10 and endokinin C.
Other Names: Aminopeptidase Q, AP-Q, 3411-, CHL2 antigen, Laeverin, AQPEP, LVRN
Target/Specificity:
This AQPEP antibody is generated from a rabbit immunized with a KLH conjugated synthetic peptide between 844-877 amino acids from human AQPEP.
Dilution: 1:2000
Calculated MW: 113283
Gene Name: LVRN (HGNC:26904)
Gene ID: 206338
Primary Accession: Q6Q4G3
Format: Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
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