CD59 Mouse Monoclonal Antibody [Clone ID: OTI2E11]

CAT#: TA507349

CD59 mouse monoclonal antibody, clone OTI2E11 (formerly 2E11)

Size: 30 ul 100 ul

Formulation: Standard Carrier-Free

Conjugation: Unconjugated Biotin HRP



  View other "OTI2E11" antibodies (4)

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【特别福利】购一抗正装产品,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
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Recombinant protein of human CD59 molecule, complement regulatory protein (CD59), transcript variant 2, 20 µg
    • 20 ug

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Transient overexpression lysate of CD59 molecule, complement regulatory protein (CD59), transcript variant 5
    • 100 ug

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Recombinant protein of human CD59 molecule, complement regulatory protein (CD59), transcript variant 2, 100 µg
    • 100 ug

CNY 9,998.00


Transient overexpression lysate of CD59 molecule, complement regulatory protein (CD59), transcript variant 2
    • 100 ug

CNY 3,080.00

Specifications

Product Data
Clone Name OTI2E11
Applications WB
Recommend Dilution WB 1:4000
Reactivity Human
Host Mouse
Clonality Monoclonal
Immunogen Full length human recombinant protein of human CD59(NP_000602) produced in HEK293T cell.
Formulation PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Concentration 1 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 11.6 kDa
Gene Name CD59 molecule (CD59 blood group)
Background This gene encodes a cell surface glycoprotein that regulates complement-mediated cell lysis, and it is involved in lymphocyte signal transduction. This protein is a potent inhibitor of the complement membrane attack complex, whereby it binds complement C8 and/or C9 during the assembly of this complex, thereby inhibiting the incorporation of multiple copies of C9 into the complex, which is necessary for osmolytic pore formation. This protein also plays a role in signal transduction pathways in the activation of T cells. Mutations in this gene cause CD59 deficiency, a disease resulting in hemolytic anemia and thrombosis, and which causes cerebral infarction. Multiple alternatively spliced transcript variants, which encode the same protein, have been identified for this gene. [provided by RefSeq, Jul 2008]
Synonyms 1F5; 16.3A5; EJ16; EJ30; EL32; G344; HRF-20; HRF20; MAC-IP; MACIF; MEM43; MIC11; MIN1; MIN2
Reference Data
Protein Families Druggable Genome
Protein Pathways Complement and coagulation cascades, Hematopoietic cell lineage
*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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