SMNDC1 Antikörper
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- Target Alle SMNDC1 Antikörper anzeigen
- SMNDC1 (Survival Motor Neuron Domain Containing 1 (SMNDC1))
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser SMNDC1 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), ELISA
- Aufreinigung
- Antibody is purified by peptide affinity chromatography method.
- Immunogen
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SMNDC1.
- Top Product
- Discover our top product SMNDC1 Primärantikörper
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- Applikationshinweise
- SMNDC1 antibody can be used for detection of SMNDC1 by ELISA at 1:1562500. SMNDC1 antibody can be used for detection of SMNDC1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Lyophilized
- Rekonstitution
- Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
- Konzentration
- 1 mg/mL
- Buffer
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
- Handhabung
- As with any antibody avoid repeat freeze-thaw cycles.
- Lagerung
- 4 °C/-20 °C
- Informationen zur Lagerung
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store SMNDC1 antibody at -20 °C.
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- Target
- SMNDC1 (Survival Motor Neuron Domain Containing 1 (SMNDC1))
- Andere Bezeichnung
- SMNDC1 (SMNDC1 Produkte)
- Synonyme
- smnr antikoerper, spf30 antikoerper, SMNDC1 antikoerper, SMNR antikoerper, SPF30 antikoerper, TDRD16C antikoerper, wu:fb37h07 antikoerper, wu:fc23a07 antikoerper, 2410004J23Rik antikoerper, 4933440I19Rik antikoerper, survival motor neuron domain containing 1 antikoerper, smndc1 antikoerper, SMNDC1 antikoerper, Bm1_41545 antikoerper, Smndc1 antikoerper
- Hintergrund
- This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. SMNDC1 is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene. This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene.
- Molekulargewicht
- 27 kDa
- Gen-ID
- 10285
- NCBI Accession
- NP_005862
- UniProt
- O75940
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