Comparison

Laminin Rhodamine (mouse tumor)

Item no. LMN01-B
Manufacturer Cytoskeleton
Amount 20 x 20 ug
Quantity options 5 x 20 ug 20 x 20 ug
Category
Type Proteins
Specific against Mouse (Murine, Mus musculus)
Purity Purity is determined by scanning densitometry of proteins on SDS-PAGE gels. Samples are >90% pure. <br />Legend: 20 ?g of unlabeled laminin (Lane 1) and 20 ?g of rhodamine laminin (Lane 2) was separated by electrophoresis in a 4-20% SDS-PAGE system. The u
Citations 1. Kelly T. et al. 1994. Invadopodia promote proteolysis of a wide variety of extracellular matrix proteins. J. Cellular Physiol.158: 299-308.
2. Tronchin G. et al. 1997. Expression and identification of a laminin-binding protein in Aspergillus fumigates conidia. Infection & Immunity65: 9-15.
ECLASS 10.1 32160409
ECLASS 11.0 32160409
UNSPSC 12352202
Alias Laminin, rhodamine laminin, red laminin, fluorescent laminin
Similar products Laminin, rhodamine laminin, red laminin, fluorescent laminin
Shipping Condition Room temperature
Available
Shipping Temperature
AT
Storage Conditions
On Arrival: 4°C
Delivery Time
1-2 Weeks
FAQs

Question 1: What is the optimal excitation and emission filter settings to visualize the rhodamine fluorescence?


Answer 1: Rhodamine-labeled laminin can be detected using a filter set of 535 nm excitation and 585 nm emission.



Question 2: What is the labeling stoichiometry?


Answer 2: Rhodamine labeling stoichiometry was calculated to be 2-5 dyes per laminin protein using the absorbancy maximum for rhodamine at 565 nm and the Beer-Lambert law. Dye extinction coefficient when protein bound is 70, 000 M-1cm-1.

Weight (grams)
60
Product Uses
Cell invasion assays (1)
FACS analysis of laminin binding cells (2)
Cell invasion assays (1)
FACS analysis of laminin binding cells (2)
Cell invasion assays (1)
FACS analysis of laminin binding cells (2)
Material
Laminin-1 is purified from EHS tumor tissue and is free of the laminin binding protein entactin which is a common contaminant in some laminin preparations (150 kDa). Protein purity is determined by scanning densitometry of Coomassie Blue stained protein on a 4-20% polyacrylamide gel. The laminin is >90% pure (Figure 1).
The protein is modified to contain covalently linked rhodamines at random surface lysines. An activated ester of rhodamine (5-(and 6)-carboxytetramethylrhodamine succinimidyl ester is used to label the protein. Labeling stoichiometry is determined by spectroscopic measurement of protein and dye concentrations. Final labeling stoichiometry is 2-5 dyes per protein molecule (Figure 2). The material is guaranteed to contain <15% of free dye and >85% of dye conjugated to laminin. Rhodamine laminin can be detected using a filter set of 535 nm excitation and 585 nm emission.
Laminin runs as individual subunits on SDS-PAGE with an apparent molecular weight of 400 and 225 kDa (Figure 1). LMN01 is supplied as a pale pink lyophilized powder. Each vial of LMN01 contains 20 ?g protein.
Figure 1 Legend
Legend: LMN01 was diluted with Milli-Q water and its absorbance spectrum was scanned between 250 and 750 nm. In this example, rhodamine labeling stoichiometry was calculated to be 2.7 dyes per laminin protein using the absorbancy maximum for rhodamine at 565 nm and the Beer-Lambert law. Dye extinction coefficientWhen protein bound is 70, 000M-1cm-1

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 20 x 20 ug
Available: In stock
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