PRSS12 Antibody

Code CSB-PA018812LA01HU
Size US$166
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  • Immunohistochemistry of paraffin-embedded human brain tissue using CSB-PA018812LA01HU at dilution of 1:100

  • Immunohistochemistry of paraffin-embedded human lung tissue using CSB-PA018812LA01HU at dilution of 1:100

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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) PRSS12 Polyclonal antibody
Uniprot No.
Target Names
PRSS12
Alternative Names
BSSP 3 antibody; BSSP3 antibody; Leydin antibody; MGC12722 antibody; Motopsin antibody; MRT1 antibody; NETR_HUMAN antibody; Neurotrypsin antibody; protease; serine; 12 (neurotrypsin; motopsin) antibody; Prss12 antibody; Serine protease 12 antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Recombinant Human Neurotrypsin protein (631-874AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated

The PRSS12 Antibody (Product code: CSB-PA018812LA01HU) is Non-conjugated. For PRSS12 Antibody with conjugates, please check the following table.

Available Conjugates
Conjugate Product Code Product Name Application
HRP CSB-PA018812LB01HU PRSS12 Antibody, HRP conjugated ELISA
FITC CSB-PA018812LC01HU PRSS12 Antibody, FITC conjugated
Biotin CSB-PA018812LD01HU PRSS12 Antibody, Biotin conjugated ELISA
Clonality
Polyclonal
Isotype
IgG
Purification Method
>95%, Protein G purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
Form
Liquid
Tested Applications
ELISA, IHC
Recommended Dilution
Application Recommended Dilution
IHC 1:20-1:200
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
Usage
For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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Target Background

Function
Plays a role in neuronal plasticity and the proteolytic action may subserve structural reorganizations associated with learning and memory operations.
Gene References into Functions
  1. 4-base pair deletion in the neurotrypsin gene was associated with autosomal recessive nonsyndromic mental retardation; findings suggest that neurotrypsin-mediated proteolysis is required for normal synaptic function PMID: 12459588
Involvement in disease
Mental retardation, autosomal recessive 1 (MRT1)
Subcellular Location
Secreted.
Protein Families
Peptidase S1 family
Tissue Specificity
Brain and Leydig cells of the testis.
Database Links

HGNC: 9477

OMIM: 249500

KEGG: hsa:8492

STRING: 9606.ENSP00000296498

UniGene: Hs.445857

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7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA
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