GLB1L3 Antikörper (AA 51-150)
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- Target Alle GLB1L3 Produkte
- GLB1L3 (Galactosidase, beta 1-Like 3 (GLB1L3))
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Bindungsspezifität
- AA 51-150
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Reaktivität
- Maus
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser GLB1L3 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- Kreuzreaktivität
- Maus
- Homologie
- Human,Rat,Horse,Chicken
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human GLB1L3
- Isotyp
- IgG
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- Applikationshinweise
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 μg/μL
- Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- Konservierungsmittel
- ProClin
- Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Lagerung
- 4 °C,-20 °C
- Informationen zur Lagerung
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- Haltbarkeit
- 12 months
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- Target
- GLB1L3 (Galactosidase, beta 1-Like 3 (GLB1L3))
- Andere Bezeichnung
- GLB1L3 (GLB1L3 Produkte)
- Synonyme
- 4921509F24Rik antikoerper, GLB1L3 antikoerper, galactosidase, beta 1 like 3 antikoerper, galactosidase beta 1 like 2 antikoerper, galactosidase beta 1 like 3 antikoerper, galactosidase, beta 1-like 3 antikoerper, Glb1l3 antikoerper, GLB1L2 antikoerper, GLB1L3 antikoerper
- Hintergrund
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Synonyms: Beta galactosidase 1 like protein 3, Beta-galactosidase-1-like protein 3, FLJ90231, Galactosidase, beta 1 like 3, GLB1L 3, Glb1l3, GLBL3_HUMAN, LOC112937, OTTHUMP00000235427.
Background: GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
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