ODAPH Antibody

Code CSB-PA613780LA01HU
Size US$166
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  • Immunohistochemistry of paraffin-embedded human placenta tissue using CSB-PA613780LA01HU at dilution of 1:100

  • Immunohistochemistry of paraffin-embedded human bladder cancer using CSB-PA613780LA01HU at dilution of 1:100

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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) ODAPH Polyclonal antibody
Uniprot No.
Target Names
ODAPH
Alternative Names
ODAPH antibody; C4orf26 antibody; Odontogenesis associated phosphoprotein antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Recombinant Human Odontogenesis associated phosphoprotein protein (24-130AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated

The ODAPH Antibody (Product code: CSB-PA613780LA01HU) is Non-conjugated. For ODAPH Antibody with conjugates, please check the following table.

Available Conjugates
Conjugate Product Code Product Name Application
HRP CSB-PA613780LB01HU ODAPH Antibody, HRP conjugated ELISA
FITC CSB-PA613780LC01HU ODAPH Antibody, FITC conjugated
Biotin CSB-PA613780LD01HU ODAPH 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.

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Target Background

Function
May promote nucleation of hydroxyapatite.
Gene References into Functions
  1. Autozygosity mapping and clonal sequencing of an Omani family identified mutations in the uncharacterized gene, C4orf26, as a cause of recessive hypomineralized amelogenesis imperfecta PMID: 22901946
Involvement in disease
Amelogenesis imperfecta, hypomaturation type, 2A4 (AI2A4)
Subcellular Location
Secreted.
Tissue Specificity
Highly expressed in placenta.
Database Links

HGNC: 26300

OMIM: 614829

KEGG: hsa:152816

STRING: 9606.ENSP00000406925

UniGene: Hs.24510

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