SEARCH OUR PRODUCT CATALOG

F13A1 Break Apart FISH Probe

Empire Genomics’ F13A1 Break Apart FISH Probe is designed to flank the F13A1 gene and is typically used for detecting F13A1 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in green and orange by default, but may be customized to meet your needs.

** This product is for in vitro and research use only. This product is not intended for diagnostic use.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
F13A1BA-20-GROR  (Standard Design) 20 (40 μL) 200 μL
F13A1BA-20-AQOR 20 (40 μL) 200 μL
F13A1BA-20-GOGR 20 (40 μL) 200 μL
F13A1BA-20-GORE 20 (40 μL) 200 μL
F13A1BA-20-GRGO 20 (40 μL) 200 μL
F13A1BA-20-GRRE 20 (40 μL) 200 μL
F13A1BA-20-ORGR 20 (40 μL) 200 μL
F13A1BA-20-REGO 20 (40 μL) 200 μL
F13A1BA-20-REGR 20 (40 μL) 200 μL

Gene Summary

This gene encodes the coagulation factor XIII A subunit. Coagulation factor XIII is the last zymogen to become activated in the blood coagulation cascade. Plasma factor XIII is a heterotetramer composed of 2 A subunits and 2 B subunits. The A subunits have catalytic function, and the B subunits do not have enzymatic activity and may serve as plasma carrier molecules. Platelet factor XIII is comprised only of 2 A subunits, which are identical to those of plasma origin. Upon cleavage of the activation peptide by thrombin and in the presence of calcium ion, the plasma factor XIII dissociates its B subunits and yields the same active enzyme, factor XIIIa, as platelet factor XIII. This enzyme acts as a transglutaminase to catalyze the formation of gamma-glutamyl-epsilon-lysine crosslinking between fibrin molecules, thus stabilizing the fibrin clot. It also crosslinks alpha-2-plasmin inhibitor, or fibronectin, to the alpha chains of fibrin. Factor XIII deficiency is classified into two categories: type I deficiency, characterized by the lack of both the A and B subunits; and type II deficiency, characterized by the lack of the A subunit alone. These defects can result in a lifelong bleeding tendency, defective wound healing, and habitual abortion. [provided by RefSeq, Jul 2008]

Gene Details

Gene Symbol: F13A1

Gene Name: Coagulation Factor XIII A Chain

Chromosome: CHR6: 6144310-6320924

Locus: 6p25.1

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this gene.

Product Details

Product: F13A1 FISH Probe

Test Kits: 20 (40 μL)

ISH Buffer: 200 μL

SKU: F13A1-20-OR

Material Safety Data Sheet: MSDS.pdf

Turnaround Time: 7-10 Business Days

Shipping Time: 1-2 Day Expedited Shipping