DTNA antibody
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- Target See all DTNA Antibodies
- DTNA (Dystrobrevin alpha (DTNA))
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Reactivity
- Human
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Host
- Mouse
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Clonality
- Monoclonal
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Conjugate
- This DTNA antibody is un-conjugated
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Application
- Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS)
- Characteristics
- Homo sapiens dystrobrevin, alpha (DTNA), transcript variant 5
- Purification
- Purified from mouse ascites fluids by affinity chromatography
- Immunogen
- Full length human recombinant protein of human DTNA (NP_116761) produced in HEK293T cell.
- Clone
- 1B2
- Isotype
- IgG2a
- Top Product
- Discover our top product DTNA Primary Antibody
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- Application Notes
- WB 1:500~2000, IF 1:100, FLOW 1:100
- Comment
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The concentration of the product may vary between diferrent lots.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.5-1.0 mg/mL
- Buffer
- PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.
- Preservative
- Sodium azide
- Precaution of Use
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
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- Target
- DTNA (Dystrobrevin alpha (DTNA))
- Alternative Name
- DTNA (DTNA Products)
- Synonyms
- adtn antibody, atnb antibody, MGC146484 antibody, 2210407P21Rik antibody, A0 antibody, Dtn antibody, a-DB-1 antibody, adbn antibody, D18S892E antibody, DRP3 antibody, DTN antibody, DTN-A antibody, LVNC1 antibody, Dtna-ps1 antibody, RGD1561985 antibody, dystrobrevin alpha antibody, dystrobrevin, alpha antibody, DTNA antibody, dtna antibody, LOC100195747 antibody, Dtna antibody
- 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.
- Molecular Weight
- 58.7 kDa
- Gene ID
- 1837
- NCBI Accession
- NM_032979
- HGNC
- 1837
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