LAMB3 Antibody (OAGA00253)

Catalog No: OAGA00253

Size:100 ul

Sample (30 ug of whole cell lysate)
A: A431
7.5% SDS PAGE
Laminin beta-3 antibody
OAGA00253 diluted at 1:1000

Sample (30 ug of whole cell lysate)
A:NIH-3T3
7.5% SDS PAGE
OAGA00253 diluted at 1:1000

Immunohistochemical analysis of paraffin-embedded Lung ca, using Laminin beta 3(OAGA00253) antibody at 1:250 dilution.

Immunofluorescence analysis of methanol-fixed HeLa, using Laminin beta 3(OAGA00253) antibody at 1:200 dilution.

Product Info

• Predicted Species Reactivity: Human, Mouse
• Product Format: Liquid. 0.1M Tris, 0.1M Glycine, 10% Glycerol (pH7). 0.01% Thimerosal was added as a preservative.
• Clonality: Polyclonal
• Isotype: IgG
• Host: Rabbit
• Application: ICC, IF, IHC-P, WB
  Cellular Localization: Secreted , extracellular space , extracellular matrix , basement membrane.
  Positive Controls: A431 , H1299 , HeLa , HepG2 , NIH-3T3
  
• Reconstitution and Storage: Keep as concentrated solution. Aliquot and store at -20C or below. Avoid multiple freeze-thaw cycles.
• Immunogen: Recombinant protein encompassing a sequence within the center region of human Laminin beta 3. The exact sequence is proprietary.
• Purification: Purified by antigen-affinity chromatography.
• Predicted Homology Based on Immunogen Sequence: Human; Mouse; Bovine
• Concentration: 0.73 mg/ml
• Intended Use: For in vitro laboratory use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.
• Application Info: ICC/IF: 1:100~1000
  IHC-P: 1:100~1000
  WB: 1:500~3000
  

Target Info

• Gene Symbol: LAMB3
• Gene Full Name: Laminin subunit beta-3
• Alias Symbols: AI1A, LAM5, LAMNB1, BM600-125KDA
• NCBI Gene Id: 3914
• Protein Name: Laminin subunit beta-3
• Description of Target: The product encoded by this gene is a laminin that belongs to a family of basement membrane proteins. This protein is a beta subunit laminin, which together with an alpha and a gamma subunit, forms laminin-5. Mutations in this gene cause epidermolysis bullosa junctional Herlitz type, and generalized atrophic benign epidermolysis bullosa, diseases that are characterized by blistering of the skin. Multiple alternatively spliced transcript variants that encode the same protein have been found for this gene.
• Uniprot ID: Q13751
• Protein Accession #: NP_000219.2
• Molecular Weight: 130 kDa