GTX00807
CLCN7 antibody
Eine Lieferung in diese Region ist nicht möglich.
- SKU:
- GTX00807
- Zusätzliche Namen:
- CLC7 , CLCN7 , OPTA2 , OPTB4 , PPP1R63 , chloride voltagegated channel 7 , chloride voltage-gated channel 7
- Anwendung:
- WB, IF, ICC
- Konzentration:
- 1 mg/ml
- 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:
- PBS, 150mM NaCl, 50% Glycerol, 0.02% Sodium azide.
- Immunogen:
- A synthesized peptide derived from human CLCN7, corresponding to a region within N-terminal amino acids.
- Uniprot:
- P51798
- Synonyme:
- chloride channel 7 alpha subunit;chloride channel protein 7;chloride channel, voltage-sensitive 7;CLC-7;CLC7;H(+)/Cl(-) exchange transporter 7;HOD;OPTA2;OPTB4;PPP1R63;protein phosphatase 1, regulatory subunit 63
- Weitere Details:
- The product of this gene belongs to the CLC chloride channel family of proteins. Chloride channels play important roles in the plasma membrane and in intracellular organelles. This gene encodes chloride channel 7. Defects in this gene are the cause of osteopetrosis autosomal recessive type 4 (OPTB4), also called infantile malignant osteopetrosis type 2 as well as the cause of autosomal dominant osteopetrosis type 2 (OPTA2), also called autosomal dominant Albers-Schonberg disease or marble disease autosoml dominant. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. OPTA2 is the most common form of osteopetrosis, occurring in adolescence or adulthood. [provided by RefSeq, Jul 2008]
- Versandbedingungen:
- Blue Ice