SHOX Antikörper (N-Term)
Kurzübersicht für SHOX Antikörper (N-Term) (ABIN2777838)
Target
Alle SHOX Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- N-Term
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Verwendungszweck
- SHOX Antibody - N-terminal region
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Sequenz
- EELTAFVSKS FDQKSKDGNG GGGGGGGKKD SITYREVLES GLARSRELGT
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Homologie
- Cow: 93%, Dog: 100%, Guinea Pig: 82%, Horse: 93%, Human: 100%, Mouse: 82%, Pig: 100%, Rat: 82%, Zebrafish: 90%
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Produktmerkmale
- This is a rabbit polyclonal antibody against SHOX. It was validated on Western Blot using a cell lysate as a positive control.
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Aufreinigung
- Affinity Purified
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Immunogen
- The immunogen is a synthetic peptide directed towards the N terminal region of human SHOX
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Applikationshinweise
- Optimal working dilution should be determined by the investigator.
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Kommentare
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP33284-100UG
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- 0.5 mg/mL
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Buffer
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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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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Handhabung
- prevent freeze-thaw cycles
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Lagerung
- 4 °C,-20 °C
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Informationen zur Lagerung
- For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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- SHOX (Short Stature Homeobox (SHOX))
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Andere Bezeichnung
- SHOX
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Hintergrund
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Background Information: This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies.This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.
Gene Name: Short stature homeobox
Alternative Symbols: SS, GCFX, PHOG, SHOXY
Protein Name: Short stature homeobox protein
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Molekulargewicht
- 32kDa
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Gen-ID
- 6473
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NCBI Accession
- NP_000442
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UniProt
- O15266
Target
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