RNF152 Antibody F-4 è un monoclonale di topo IgG1 κ, citato in 1 pubblicazioni, fornito in 200 µg/ml
generato contro gli amminoacidi 65-130 mappati nella regione interna di RNF152 di origine human
raccomandato per il rilevamento di RNF152 di origine mouse, rat e human in WB, IP, IF e ELISA
m-IgG1 BP-HRP and m-IgGκ BP-HRP are the preferred secondary detection reagents for RNF152 Antibody (F-4) for WB applications. These reagents are now offered in bundles with RNF152 Antibody (F-4) (see ordering information below).
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
The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in the ubiquitination pathway of protein degradation. RNF152 (ring finger protein 152) is a 203 amino acid protein that contains one RING-type zinc finger and may be involved in protein degradation events throughout the cell. The gene encoding RNF152 maps to human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.