Every item is shipped based on the best shipping method assessed for the temperature requirements of that specific item. Items are grouped and shipped together whenever
possible, and a separate shipping charge will be included for each shipping method required. Shipping charges listed below are from our US warehouses to the Contiguous US,
Alaska, Hawaii, Canada and Puerto Rico. Shipping charges for countries outside the US and Canada will be determined once order has been received
Please note: We can not ship to PO boxes
Express Blue Ice
Express Dry Ice
Animal Health Prescription Item
SHIPPING METHODS & CHARGES
Ships via FedEx Ground to Contiguous US, Alaska, Canada, Monday through Friday. This method is used for less temperature sensitive items such as lab ware and animal
health products, bulky and/or heavy items
Labware ships FedEx Ground free of charge to the contiguous US
FOXL2 Antibody (262C1a) is a high quality monoclonal FOXL2 antibody (also designated FOXL2 antibody) suitable for the detection of the FOXL2 protein of human origin. FOXL2 Antibody (262C1a) is available as the non-conjugated anti-FOXL2 antibody. FOXL2 is a 376 amino acid protein encoded by the human gene FOXL2. FOXL2 is found in the nucleus and is believed to be a transcriptional regulator. Defects in FOXL2 are a cause of blepharophimosis, ptosis and epicanthus inversus syndrome (BPES), also known as blepharophimosis syndrome. BPES is an autosomal dominant disorder characterized by eyelid dysplasia, small palpebral fissures, drooping eyelids and a skin fold running inward and upward from the lower lid. In type I BPSE (BPES1) eyelid abnormalities are associated with female infertility. Affected females show an ovarian deficit due to primary amenorrhea or to premature ovarian failure (POF). In type II BPSE (BPES2) affected individuals show only the eyelid defects. There is a mutational hotspot in the region coding for the poly-Ala domain, since 30% of all mutations in the ORF lead to poly-Ala expansions, resulting mainly in BPES type II. Defects in FOXL2 are also a cause of premature ovarian failure 3 (POF3). POF is a defect of ovarian development and is characterized by hypoestrogenism, primary or secondary amenorrhea, elevated levels of serum gonadotropins or early menopause. POF is defined as the cessation of ovarian function under the age of 40 years.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.