![VWF antibody [VWF635]](https://www.genetex.com/upload/website/prouct_img/normal/GTX35166/GTX35166_20200115_IHC-P_321_w_23060819_354.webp)
![VWF antibody [VWF635]](https://www.genetex.com/upload/website/prouct_img/normal/GTX35166/GTX35166_IHC-P_1_w_23060819_467.webp)
GTX35166
VWF antibody [VWF635]
Cannot supply to this region.
- SKU:
- GTX35166
- Additional Names:
- F8VWF , VWD , VWF , von Willebrand factor , von Willebrand Factor
- Application:
- IHC-P
- Concentration:
- 0.2 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- protein a/g purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Mouse
- Reactivities:
- Human
- Buffer:
- PBS, 0.05% BSA, 0.05% Sodium azide.
- Immunogen:
- Recombinant human vWF fragment spanning around aa 845-949 (exact sequence is proprietary)
- Clone:
- VWF635
- Uniprot:
- P04275
- Synonyms:
- coagulation factor VIII VWF;F8VWF;von Willebrand factor;VWD
- Extra Details:
- This gene encodes a glycoprotein involved in hemostasis. The encoded preproprotein is proteolytically processed following assembly into large multimeric complexes. These complexes function in the adhesion of platelets to sites of vascular injury and the transport of various proteins in the blood. Mutations in this gene result in von Willebrand disease, an inherited bleeding disorder. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq, Oct 2015]
- Shipping Conditions:
- Blue Ice