GTX89771
CMG1 antibody, C-term
Cannot supply to this region.
- SKU:
- GTX89771
- Additional Names:
- intraflagellar transport 74 , BBS20 , CCDC2 , CMG-1 , CMG1
- Application:
- WB, IHC-P, IF, ICC
- Concentration:
- 0.50 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Ammonium Sulfate Precipitated; 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:
- Goat
- Reactivities:
- Human, Rat
- Buffer:
- TBS, 0.5% BSA, 0.02% Sodium azide.
- Immunogen:
- Peptide with sequence C-KTIVDALHSTSGN, from the C Terminus of the protein sequence according to NP_001092692.1; NP_001092693.1; NP_079379.2; AAK77221.1.
- Uniprot:
- Q96LB3
- Synonyms:
- BBS22;capillary morphogenesis gene 1 protein;capillary morphogenesis protein 1;CCDC2;CMG-1;CMG1;coiled-coil domain containing 2;coiled-coil domain-containing protein 2;intraflagellar transport 74 homolog;intraflagellar transport protein 74 homolog
- Extra Details:
- This gene encodes a core intraflagellar transport (IFT) protein which belongs to a multi-protein complex involved in the transport of ciliary proteins along axonemal microtubules. IFT proteins are found at the base of the cilium as well as inside the cilium, where they assemble into long arrays between the ciliary base and tip. This protein, together with intraflagellar transport protein 81, binds and transports tubulin within cilia and is required for ciliogenesis. Naturally occurring mutations in this gene are associated with amyotrophic lateral sclerosis--frontotemporal dementia and Bardet-Biedl Syndrome. [provided by RefSeq, Mar 2017]
- Shipping Conditions:
- Blue Ice