PRSS1 purified MaxPab rabbit polyclonal antibody (D01P)
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More Files
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Specification
Product Description
Rabbit polyclonal antibody raised against a full-length human PRSS1 protein.
Immunogen
PRSS1 (NP_002760.1, 1 a.a. ~ 247 a.a) full-length human protein.
Sequence
MNPLLILTFVAAALAAPFDDDDKIVGGYNCEENSVPYQVSLNSGYHFCGGSLINEQWVVSAGHCYKSRIQVRLGEHNIEVLEGNEQFINAAKIIRHPQYDRKTLNNDIMLIKLSSRAVINARVSTISLPTAPPATGTKCLISGWGNTASSGADYPDELQCLDAPVLSQAKCEASYPGKITSNMFCVGFLEGGKDSCQGDSGGPVVCNGQLQGVVSWGDGCAQKNKPGVYTKVYNYVKWIKNTIAANS
Host
Rabbit
Reactivity
Human
Interspecies Antigen Sequence
Mouse (79)
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Tissue lysate)
PRSS1 MaxPab rabbit polyclonal antibody. Western Blot analysis of PRSS1 expression in human pancreas.Western Blot (Transfected lysate)
Western Blot analysis of PRSS1 expression in transfected 293T cell line (H00005644-T02) by PRSS1 MaxPab polyclonal antibody.
Lane 1: PRSS1 transfected lysate(26.60 KDa).
Lane 2: Non-transfected lysate.
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Gene Info — PRSS1
Entrez GeneID
5644GeneBank Accession#
NM_002769.2Protein Accession#
NP_002760.1Gene Name
PRSS1
Gene Alias
MGC120175, MGC149362, TRP1, TRY1, TRY4, TRYP1
Gene Description
protease, serine, 1 (trypsin 1)
Gene Ontology
HyperlinkGene Summary
This gene encodes a trypsinogen, which is a member of the trypsin family of serine proteases. This enzyme is secreted by the pancreas and cleaved to its active form in the small intestine. It is active on peptide linkages involving the carboxyl group of lysine or arginine. Mutations in this gene are associated with hereditary pancreatitis. This gene and several other trypsinogen genes are localized to the T cell receptor beta locus on chromosome 7. [provided by RefSeq
Other Designations
cationic trypsinogen|digestive zymogen|nonfunctional trypsin 1|protease, serine, 1|serine protease 1|trypsin I|trypsinogen 1|trypsinogen A
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Interactome
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Pathway
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Disease
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