Anti-Sar1a Antibody K-44 è un monoclonale di topo IgG2b κ Sar1a antibody, citato in 1 pubblicazioni, fornito in 100 µg/ml
generato contro il ricombinante Sar1a di origine human
raccomandato per il rilevamento di Sar1a di origine mouse, rat e human in WB e IP
Contattaci per ricevere un FREE 10 µg sample di Sar1a (K-44): sc-130463.
m-IgG2b BP-HRP and m-IgGκ BP-HRP are the preferred secondary detection reagents for Sar1a Antibody (K-44) for WB applications. These reagents are now offered in bundles with Sar1a Antibody (K-44) (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
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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
Sar1a Antibody (K-44) is a high quality monoclonal Sar1a antibody (also designated Sar1a antibody) suitable for the detection of the Sar1a protein of mouse, rat and human origin. Sar1a Antibody (K-44) is available as the non-conjugated anti-Sar1a antibody. There are a number of components involved in the secretory pathway of cells. Vesicular traffic within the early secretory pathway is mediated by COPI- and COPII-coated vesicles. The COPII vesicle coat protein promotes the formation of endoplasmic reticulum (ER) derived transport vesicles that carry secretory proteins to the Golgi complex. The SAR1 gene encodes two isoforms, Sar1a and Sar1B, in mammalian cells. These proteins are low-molecular-weight GTPases, which are essential for the formation of transport vesicles from the ER. Mutations in the SAR1 gene result in Anderson′s disease (and/or chylomicron retention disease CMRD), a rare, autosomal recessive lipid malabsorption disorder characterized by chronic diarrhea, failure to thrive and hypocholesterolemia in childhood.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.