MKKS Antikörper
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- Target Alle MKKS Antikörper anzeigen
- MKKS (McKusick-Kaufman Syndrome (MKKS))
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Reaktivität
- Human, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser MKKS Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB)
- Kreuzreaktivität
- Human, Ratte
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant protein corresponding to Mouse MKKS
- Top Product
- Discover our top product MKKS Primärantikörper
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anti-McKusick-Kaufman Syndrome (MKKS) (AA 1-570) antibody
MKKS Reaktivität: Human WB, IP Wirt: Kaninchen Polyclonal unconjugated
anti-McKusick-Kaufman Syndrome (MKKS) antibodyMKKS Reaktivität: Human ELISA, IHC Wirt: Kaninchen Polyclonal unconjugated
anti-McKusick-Kaufman Syndrome (MKKS) (AA 1-570) antibodyMKKS Reaktivität: Human WB Wirt: Maus Polyclonal unconjugated
anti-McKusick-Kaufman Syndrome (MKKS) (AA 221-570) antibodyMKKS Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
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- Applikationshinweise
- WB (H,R) 1:1000-1:2000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Buffer
- PBS, pH 7.4, 0.02 % sodium azide
- 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
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- Target
- MKKS (McKusick-Kaufman Syndrome (MKKS))
- Andere Bezeichnung
- MKKS (MKKS Produkte)
- Synonyme
- bbs6 antikoerper, zgc:55608 antikoerper, MKKS antikoerper, kms antikoerper, mks antikoerper, hmcs antikoerper, DKFZp459L0833 antikoerper, BBS6 antikoerper, HMCS antikoerper, KMS antikoerper, MKS antikoerper, 1300013E18Rik antikoerper, AI463362 antikoerper, AI957237 antikoerper, Bbs6 antikoerper, McKusick-Kaufman syndrome antikoerper, Mkks antikoerper, mkks antikoerper, MKKS antikoerper
- Hintergrund
- MKKS also known as BBS6 is a probable chaperone given to the amino acid similarity to the chaperonin family of proteins and may play a role in protein processing in limb, cardiac and reproductive system development. The mutations in BBS6 have been linked to Bardet-Biedl syndrome (BBS) which is a genetically heterogeneous, autosomal recessive disorder characterized by usually severe pigmentary retinopathy, early onset obesity, polydactyly, hypogenitalism, renal malformation and mental retardation. It may also get involved in cellular organization processes, in particular relating to ciliary/flagellar and centrosomal activities.
- Molekulargewicht
- 62 kDa
- Gen-ID
- 59030
- NCBI Accession
- NP_001135418
- UniProt
- Q9JI70
- Pathways
- Sensory Perception of Sound
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