![EVC2 antibody [C3], C-term](https://www.genetex.com/upload/website/prouct_img/normal/GTX107725/GTX107725_39721_IFA_w_23060120_748.webp)
![EVC2 antibody [C3], C-term](https://www.genetex.com/upload/website/prouct_img/normal/GTX107725/GTX107725_WB_w_23060120_198.webp)
GTX107725
EVC2 antibody [C3], C-term
Cannot supply to this region.
- SKU:
- GTX107725
- Additional Names:
- EvC ciliary complex subunit 2 , LBN , WAD
- Application:
- WB, IF, ICC
- Concentration:
- 1 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity 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:
- Rabbit
- Reactivities:
- Human
- Buffer:
- 0.1M Tris, 0.1M Glycine, 10% Glycerol, 0.01% Thimerosal.
- Immunogen:
- Synthetic peptide encompassing a sequence within the Intracellular domain of human EVC2. The exact sequence is proprietary.
- Clone:
- C3
- Uniprot:
- Q86UK5
- Synonyms:
- Ellis van Creveld syndrome 2;ellis-van Creveld syndrome protein 2;LBN;limbin;WAD
- Extra Details:
- This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq]
- Shipping Conditions:
- Blue Ice