VWA3B Antibody

Code CSB-PA681377LA01HU
Size US$166
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  • Immunohistochemistry of paraffin-embedded human skin tissue using CSB-PA681377LA01HU at dilution of 1:100

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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) VWA3B Polyclonal antibody
Uniprot No.
Target Names
VWA3B
Alternative Names
VWA3B antibody; von Willebrand factor A domain-containing protein 3B antibody; VWA domain-containing protein 3B antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Recombinant Human von Willebrand factor A domain-containing protein 3B protein (1-160AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated

The VWA3B Antibody (Product code: CSB-PA681377LA01HU) is Non-conjugated. For VWA3B Antibody with conjugates, please check the following table.

Available Conjugates
Conjugate Product Code Product Name Application
HRP CSB-PA681377LB01HU VWA3B Antibody, HRP conjugated ELISA
FITC CSB-PA681377LC01HU VWA3B Antibody, FITC conjugated
Biotin CSB-PA681377LD01HU VWA3B 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

Gene References into Functions
  1. Mutated VWA3B was found to be likely associated with cerebellar degeneration with intellectual disability. Although a rare cause of cerebellar degeneration, these findings indicate a critical role for VWA3B in the apoptosis pathway in neuronal tissues. PMID: 26157035
Involvement in disease
Spinocerebellar ataxia, autosomal recessive, 22 (SCAR22)
Subcellular Location
Cytoplasm.
Database Links

HGNC: 28385

OMIM: 614884

KEGG: hsa:200403

STRING: 9606.ENSP00000417955

UniGene: Hs.269977

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