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

Ordering

Wt. Vol. Conc. Price
100 µg - - $635
Inquire for larger quantities

LSBio (Direct) LSBio (Direct)
206-374-1102
866-206-6909
Orders@LSBio.com
 

Most Popular C4.4A / LYPD3 Antibodies

Anti-C4.4A / LYPD3 Antibody (C-Terminus) IHC-plus™ LS-A9856
Rabbit Polyclonal to Human C4.4A / LYPD3
Human
IHC - Paraffin
Unconjugated
Immunohistochemistry Image
Anti-C4.4A / LYPD3 Antibody (aa262-311) LS-C186776
Rabbit Polyclonal to Human C4.4A / LYPD3
Human
Western blot
Unconjugated
Western blot Image

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

Details

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

Applications

  • 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.

Packaging

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: United States
Date Requested: 12/7/2016

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