Dystrobrevin alpha (DTNA) Mouse Monoclonal Antibody [Clone ID: OTI1A2]

CAT#: TA502207

DTNA (Dystrobrevin alpha) mouse monoclonal antibody, clone OTI1A2 (formerly 1A2)

Size: 30 ul 100 ul

Formulation: Standard Carrier-Free

Conjugation: Unconjugated Biotin HRP



  View other "OTI1A2" antibodies (5)

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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

Product images

经常一起买 (5)
beta Actin Mouse Monoclonal Antibody, Clone OTI1, Loading Control
    • 30 ul

CNY 300.00
CNY 1,430.00


Recombinant protein of human dystrobrevin, alpha (DTNA), transcript variant 1, 20 µg
    • 20 ug

CNY 2,900.00
CNY 6,650.00


Transient overexpression lysate of dystrobrevin, alpha (DTNA), transcript variant 11
    • 100 ug

CNY 4,840.00


Recombinant protein of human dystrobrevin, alpha (DTNA), transcript variant 5, 100 µg
    • 100 ug

CNY 9,998.00


Transient overexpression lysate of dystrobrevin, alpha (DTNA), transcript variant 5
    • 100 ug

CNY 4,840.00

Specifications

Product Data
Clone Name OTI1A2
Applications FC, IF, WB
Recommend Dilution WB 1:2000, IF 1:100, FLOW 1:100
Reactivity Human, Mouse, Rat
Host Mouse
Clonality Monoclonal
Immunogen Full length human recombinant protein of human DTNA (NP_116761) produced in HEK293T cell.
Formulation PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Concentration 0.66 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 58.7 kDa
Gene Name dystrobrevin alpha
Background The protein encoded by this gene belongs to the dystrobrevin subfamily of the dystrophin family. This protein is a component of the dystrophin-associated protein complex (DPC), which consists of dystrophin and several integral and peripheral membrane proteins, including dystroglycans, sarcoglycans, syntrophins and alpha- and beta-dystrobrevin. The DPC localizes to the sarcolemma and its disruption is associated with various forms of muscular dystrophy. Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq]
Synonyms D18S892E; DRP3; DTN; DTN-A; LVNC1
Reference Data
Protein Families Druggable Genome
*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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