GTX55177
CYLN2 antibody
Eine Lieferung in diese Region ist nicht möglich.
- SKU:
- GTX55177
- Zusätzliche Namen:
- CAP-Gly domain containing linker protein 2 , CLIP , CLIP-115 , CYLN2 , WBSCR3 , WBSCR4 , WSCR3 , WSCR4
- Anwendung:
- WB
- Physischer Zustand:
- Liquid
- Spezies-Reaktivität:
- Human
- Aufreinigung:
- Affinity Purified
- Lagerbedingungen:
- -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.
- Hersteller:
- Genetex
- Host:
- Rabbit
- Reaktivitäten:
- Human
- Buffer:
- 0.42% Potassium Phosphate, 0.87% NaCl, 30% Glycerol, 0.01% Sodium azide.
- Immunogen:
- KLH-conjugated synthetic peptide encompassing a sequence within the C-term region of CYLN2. The exact sequence is proprietary.
- Uniprot:
- Q9UDT6
- Synonyme:
- CAP-Gly domain-containing linker protein 2;CLIP;CLIP-115;CYLN2;cytoplasmic linker 2;cytoplasmic linker protein 115;cytoplasmic linker protein 2;testicular tissue protein Li 40;WBSCR3;WBSCR4;williams-Beuren syndrome chromosomal region 3 protein;williams-Beuren syndrome chromosomal region 4 protein;Williams-Beuren syndrome chromosome region 3;Williams-Beuren syndrome chromosome region 4;WSCR3;WSCR4
- Weitere Details:
- The protein encoded by this gene belongs to the family of cytoplasmic linker proteins, which have been proposed to mediate the interaction between specific membranous organelles and microtubules. This protein was found to associate with both microtubules and an organelle called the dendritic lamellar body. This gene is hemizygously deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq, Jul 2008]
- Versandbedingungen:
- Blue Ice