EPM2AIP1 Mouse Monoclonal Antibody [Clone ID: OTI2A2]

CAT#: TA501790

EPM2AIP1 mouse monoclonal antibody, clone OTI2A2 (formerly 2A2)

Size: 30 ul 100 ul

Formulation: Standard Carrier-Free

Conjugation: Unconjugated Biotin HRP



  View other "OTI2A2" antibodies (4)

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【特别福利】购一抗正装产品(≥50ul或≥50ug),免费领10ul抗体试用装

CNY 1,999.00

CNY 2,700.00


货期*
现货

规格
    • 100 ul

经常一起买 (4)
Transient overexpression lysate of EPM2A (laforin) interacting protein 1 (EPM2AIP1)
    • 100 ug

CNY 3,080.00


beta Actin Mouse Monoclonal Antibody, Clone OTI1, Loading Control
    • 30 ul

CNY 300.00
CNY 1,430.00


Recombinant protein of human EPM2A (laforin) interacting protein 1 (EPM2AIP1), 20 µg
    • 20 ug

CNY 2,900.00
CNY 6,650.00


Recombinant protein of human EPM2A (laforin) interacting protein 1 (EPM2AIP1), 100 µg
    • 100 ug

CNY 9,998.00

Specifications

Product Data
Clone Name OTI2A2
Applications FC, IHC, WB
Recommend Dilution WB 1:2000, IHC 1:150, FLOW 1:100
Reactivity Human, Mouse, Rat
Host Mouse
Clonality Monoclonal
Immunogen Full length human recombinant protein of human EPM2AIP1(NP_055620) produced in HEK293T cell.
Formulation PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Concentration 1.3 mg/ml
Purification Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
Conjugation Unconjugated
Storage Condition Store at -20°C as received.
Predicted Protein Size 70.2 kDa
Gene Name EPM2A interacting protein 1
Background The EPM2A gene, which encodes laforin, is mutated in an autosomal recessive form of adolescent progressive myoclonus epilepsy. The protein encoded by this gene binds to laforin, but its function is not known. This gene is intronless. [provided by RefSeq]. COMPLETENESS: complete on the 3' end.
Synonyms FLJ11207; KIAA0766
Reference Data
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

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