Background:PROM1, also named as PROML1, CD133 and AC133, belongs to the prominin family。 PROM1 interacts with PCDH21 and with actin filaments。 CD133 is a cance stem cell marker。 Defects in PROM1 are the cause of retinitis pigmentosa type 41 (RP41)which also known as retinal degeneration autosomal recessive prominin-related。 Defects in PROM1 are the cause of cone-rod dystrophy type 12 (CORD12)。 Defects in PROM1 are the cause of Stargardt disease type 4 (STGD4)。 Defects in PROM1 are the cause of retinal macular dys trophy type 2 (MCDR2)。 The antibody recognizes transcript variant 1,6,7 of PROM1。
幸运飞艇官网Storage/Stability:Store at 4°C or -20°C (with 50% glycerol); Minimize freeze-thaw cycles; Non-hazardous.
幸运飞艇官网Limitation:For research use only and are not intended for diagnostic or therapeutic use.
Recommended Dilutions:WB: 1:500-1000.
Applications:WB, ELISA。 Other applications have not been tested。
Formulation:Each vial at least contains 0。1 mg IgG in 0。1 ml (1 mg/ml) of PBS pH7。4 with 0。1% sodium azide。