SH3TC2 Antikörper (Internal Region)
Kurzübersicht für SH3TC2 Antikörper (Internal Region) (ABIN7225084)
Target
Alle SH3TC2 Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- Internal Region
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Verwendungszweck
- SH3TC2 Polyclonal Antibody
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Spezifität
- SH3TC2 Polyclonal Antibody detects endogenous levels of SH3TC2 protein.
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Aufreinigung
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogen
- Synthesized peptide derived from the Internal region of human SH3TC2
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Isotyp
- IgG
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Applikationshinweise
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: IHC-P (1:100-1:300), ELISA (1:40000). Not yet tested in other applications.
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Kommentare
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Primary Antibody
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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Konservierungsmittel
- Sodium azide
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Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Lagerung
- -20 °C
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Informationen zur Lagerung
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- SH3TC2 (SH3 Domain and Tetratricopeptide Repeats 2 (SH3TC2))
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Andere Bezeichnung
- SH3TC2
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Hintergrund
- Rabbit Anti-SH3TC2 Polyclonal Antibody,SH3TC2, KIAA1985, PP12494, SH3 domain and tetratricopeptide repeat-containing protein 2,SH3TC2 (SH3 domain and tetratricopeptide repeats 2) encodes a protein with two N-terminal Src homology 3 (SH3) domains and 10 tetratricopeptide repeat (TPR) motifs, and is a member of a small gene family. The gene product has been proposed to be an adapter or docking molecule. Mutations in this gene result in autosomal recessive Charcot-Marie-Tooth disease type 4C, a childhood-onset neurodegenerative disease characterized by demyelination of motor and sensory neurons.,SH3 domain and tetratricopeptide repeat-containing protein 2
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Gen-ID
- 79628
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UniProt
- Q8TF17
Target
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