| Catalog No. | Size | Price (USD) |
| 201426-T08-50 | 50 µL | $147.96 |
| 201426-T08-100 | 100 µL | $251.64 |
| 201426-T08-200 | 200 µL | $355.32 |
General Information
| Product name | Anti-GALE Antibody, Rabbit Polyclonal |
| Validated applications | IHC-P (FAQ Protocol) |
| Species reactivity | Reacts with: Human |
| Specificity | Human GALE |
| Immunogen | E. coli-derived Human GALE fragment |
| Preparation | Produced in rabbits immunized with E. coli-derived Human GALE fragment, and purified by antigen affinity chromatography. |
| Source | Polyclonal Rabbit IgG |
| Purification | Protein A & Antigen Affinity |
| Formulation | 0.2 μm filtered solution in PBS |
| Conjugate | Unconjugated |
| Form | Liquid |
| Shipping | This antibody is shipped as liquid solution at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. |
| Storage | This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles. |
Synonyms: Anti-SDR1E1 Antibody; Anti-THC13 Antibody
Image / Experimental Information
| Image 1 Description | Immunochemical staining of human GALE in human liver with rabbit polyclonal antibody at 1:100 dilution, formalin-fixed paraffin embedded sections. |
| Image 1 Alt Text | Human GALE Immunohistochemistry(IHC) 35155 |
| Image 1 URL | Source image |
| Image 2 Description | Immunochemical staining of human GALE in human liver with rabbit polyclonal antibody at 1:100 dilution, formalin-fixed paraffin embedded sections. |
| Image 2 Alt Text | Human GALE Immunohistochemistry(IHC) 35156 |
| Image 2 URL | Source image |
Background Information
| Full Name | UDP-galactose-4-epimerase |
| Description | UDP galactose-4'-epimerase, also known as GALE, enables the body to process a simple sugar called galactose, which is present in small amounts in many foods. Galactose is primarily part of a larger sugar called lactose, which is found in all dairy products and many baby formulas. UDP galactose-4'-epimerase catalyzes two distinct but analogous reactions: the epimerization of UDP-glucose to UDP-galactose, and the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine. Defects in GALE causes epimerase-deficiency galactosemia (EDG), also known as galactosemia type 3. Clinical features include early-onset cataracts, liver damage, deafness and mental retardation. |
| References |
|
-HD16JU0409-100-human-liver-IHC-P.png){kind=link}
-HD16JU0409-100-human-kidney-IHC-P.png){kind=link}