MANSC1 Antikörper
Kurzübersicht für MANSC1 Antikörper (ABIN7247171)
Target
Alle MANSC1 Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Produktmerkmale
- Polyclonal Antibody
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Aufreinigung
- Antigen affinity purification
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Immunogen
- Fusion protein of human MANSC1
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Isotyp
- IgG
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anti-MANSC Domain Containing 1 (MANSC1) (AA 27-130) antibody
MANSC1 Reaktivität: Maus WB, ELISA, IF (cc), IF (p), IHC (p), IHC (fro), ICC Wirt: Kaninchen Polyclonal unconjugated
anti-MANSC Domain Containing 1 (MANSC1) (Internal Region) antibodyMANSC1 Reaktivität: Human, Ratte WB, ELISA, IHC Wirt: Kaninchen Polyclonal unconjugated
anti-MANSC Domain Containing 1 (MANSC1) (N-Term) antibodyMANSC1 Reaktivität: Human, Rind (Kuh) WB, IHC, IHC (p) Wirt: Kaninchen Polyclonal unconjugated
anti-MANSC Domain Containing 1 (MANSC1) (AA 391-419), (C-Term) antibodyMANSC1 Reaktivität: Human WB Wirt: Kaninchen Polyclonal RB40891 unconjugated
anti-MANSC Domain Containing 1 (MANSC1) (N-Term) antibodyMANSC1 Reaktivität: Human, Maus, Rind (Kuh), Ratte, Hund, Pferd, Kaninchen WB, IHC Wirt: Kaninchen Polyclonal unconjugated
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Applikationshinweise
- IHC 1:50-1:300, ELISA 1:5000-1:10000
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- 1.8 mg/mL
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Buffer
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
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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
- Store at -20°C. Avoid freeze / thaw cycles.
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- MANSC1 (MANSC Domain Containing 1 (MANSC1))
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Andere Bezeichnung
- MANSC1
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Hintergrund
- MANSC1 (MANSC domain-containing protein 1), also known as LOH12CR3 (Loss of heterozygosity 12 chromosomal region 3 protein), is a 414 amino acid single-pass membrane protein. Expressed throughout the body, MANSC1 contains one MANSC domain and is encoded by a gene that is located on chromosome 12. Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction.
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UniProt
- Q9H8J5
Target
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