COL11A2 Antikörper
-
- Target Alle COL11A2 Antikörper anzeigen
- COL11A2 (Collagen, Type XI, alpha 2 (COL11A2))
-
Reaktivität
- Human, Maus, Ratte
-
Wirt
- Kaninchen
-
Klonalität
- Polyklonal
-
Konjugat
- Dieser COL11A2 Antikörper ist unkonjugiert
-
Applikation
- Western Blotting (WB)
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant protein of human COL11A2
- Isotyp
- IgG
- Top Product
- Discover our top product COL11A2 Primärantikörper
-
-
- Applikationshinweise
- WB 1:500 - 1:2000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
- Konzentration
- 1 mg/mL
- Buffer
- Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
-
- Target
- COL11A2 (Collagen, Type XI, alpha 2 (COL11A2))
- Andere Bezeichnung
- COL11A2 (COL11A2 Produkte)
- Synonyme
- col11a2 antikoerper, MGC89039 antikoerper, COL11A2 antikoerper, RING3 antikoerper, DFNA13 antikoerper, DFNB53 antikoerper, FBCG2 antikoerper, HKE5 antikoerper, PARP antikoerper, STL3 antikoerper, collagen, type XI, alpha 2 antikoerper, collagen type XI alpha 2 chain antikoerper, bromodomain containing 2 antikoerper, col11a2 antikoerper, COL11A2 antikoerper, BRD2 antikoerper, Col11a2 antikoerper
- Hintergrund
-
Synonyms: COBA2,COL11A2,Collagen alpha 2(XI),Collagen alpha-2(XI) chain,Collagen type XI alpha 2,Collagen XI a2,DAQB-79P13.8,DFNA13,DFNB53,FBCG2,HGNC:2187,HKE5,PARP,Pro a2 chain of collagen type XI,STL3
Background: This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. It is located on chromosome 6 very close to but separate from the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing of this type XI chain produces PARP, a proline/arginine-rich protein that is an amino terminal domain. Mutations in this gene are associated with type III Stickler syndrome, otospondylomegaepiphyseal dysplasia (OSMED syndrome), Weissenbacher-Zweymuller syndrome, autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13), and autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53). Alternative splicing results in multiple transcript variants. A related pseudogene is located nearby on chromosome 6.
- Molekulargewicht
-
Observed_MW: 150kDa
Calculated_MW: 31kDa/159-171kDa
- Gen-ID
- 1302
- UniProt
- P13942
- Pathways
- RTK Signalweg, Sensory Perception of Sound, Chromatin Binding
-