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Anti-C4.4A / LYPD3 Antibody LS-C122774


Wt. Vol. Conc. Price
100 µg - - Unavailable

Most Popular C4.4A / LYPD3 Antibodies

Anti-C4.4A / LYPD3 Antibody (C-Terminus) IHC-plus™ LS-A9856
Rabbit Polyclonal to Human C4.4A / LYPD3
IHC - Paraffin
Immunohistochemistry Image
Anti-C4.4A / LYPD3 Antibody (C-Terminus) IHC-plus™ LS-A9857
Rabbit Polyclonal to Human C4.4A / LYPD3
IHC - Paraffin
Immunohistochemistry Image
Anti-C4.4A / LYPD3 Antibody (N-Terminus) IHC-plus™ LS-A8939
Rabbit Polyclonal to Human C4.4A / LYPD3
Human, Dog, Horse, Rabbit
IHC - Paraffin
Immunohistochemistry Image

100% Guaranteed 100% Guaranteed
Goat Polyclonal (IgG) to Mouse C4.4A / LYPD3
IHC, Western blot, ELISA


Mouse C4.4A / LYPD3
Mouse (tested or 100% immunogen sequence identity)
IgG Polyclonal
Affinity purified


  • IHC (2 - 15 µg/ml)
  • Western blot (1 µg/ml)
  • ELISA (0.5 - 1 µg/ml)

Specificity and Use

C4.4A / LYPD3 antibody was raised against purified, NS0-derived, recombinant mouse C4.4A (rmC4.4A).
Recognizes mouse C4.4A. In direct ELISA, this antibody shows approximately 40% cross-reactivity with rhC4.4A/LYPD3.
Suitable for Western Blot, Immunohistochemistry and ELISA. Western Blot: 1 ug/ml. Tissue lysates were resolved by SDS-PAGE, transferred to an Immobilon-P membrane and immunoblotted. Immunohistochemistry: 2-15 ug/ml will detect C4.4A in cells and tissues. Direct ELISA: 0.5-1 ug/ml. The detection limit is ~0.3 ng/well.


Lyophilized from PBS, 5% trehalose
Sterile PBS
Lyophilized powder may be stored at -20°C. Stable for 12 months at -20°C. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Reconstituted product is stable for 12 months at -20°C.
For research use only.

About C4.4A / LYPD3

O95274 NM_014400 NP_055215.2

LYPD3 Antibody, C4.4A Antibody, MIG-C4 Antibody, LY6/PLAUR domain containing 3 Antibody

C4.4A is a structural homolog of the urokinase-type plasminogen activator receptor (uPAR). It was originally identified as a metastasis-associated membrane protein in malignant urothelium. In literature IHC studies, staining has been observed in suprabasal keratinocytes of chronic wounds and the amniotic membrane of placenta. ISH analysis demonstrated expression in urothelium of the ureter.

Requested From: 
Date Requested: 3/28/2017

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