TCTN2 Polyklonale Antilichaam, RBITC Vervoeging
Kwaliteit
ISO Gecertificeerd
Levering
24-48 uur
Technische Specificaties
Defects in TCTN2 are the cause of Meckel syndrome type 8 (MKS8) [MIM:613885]. A disorder characterized by a combination of renal cysts and variably associated features including developmental anomalies of the central nervous system (typically encephalocele), hepatic ductal dysplasia and cysts, and polydactyly.
C12orf38; FLJ12975; MKS8; OTTHUMP00000239215; OTTHUMP00000239216; Tctn2; TECT2; TECT2_HUMAN; Tectonic family member 2; Tectonic-2.
Cytoplasm, Cell membrane
• Rabbit
Mouse
61-160/697
TCTN2
• Polyclonal
• IgG
RBITC
KLH conjugated synthetic peptide derived from human TCTN2
WB, IF (IHC-P), IF (IHC-F), IF (ICC)
Purified by Protein A.
570nm/595nm
1µg/µl
WB (1:300-5000), IF (IHC-P) (1:50-200), IF (IHC-F) (1:50-200), IF (ICC) (1:50-200)
Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Unmodified
Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
Human, Rat
Beschrijving
TCTN2 Polyklonale Antilichaam, RBITC Vervoeging Beschikbaar in 100 µL. Bestel eenvoudig online met snelle levering.
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