TRAPPC2 antibody
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- Target See all TRAPPC2 Antibodies
- TRAPPC2 (Trafficking Protein Particle Complex 2 (TRAPPC2))
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Reactivity
- Human, Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This TRAPPC2 antibody is un-conjugated
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Application
- Western Blotting (WB)
- Purification
- Affinity purification
- Immunogen
- Recombinant protein of human TRAPPC2
- Isotype
- IgG
- Top Product
- Discover our top product TRAPPC2 Primary Antibody
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- Application Notes
- WB 1:500 - 1:2000
- Restrictions
- For Research Use only
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- Concentration
- 1 mg/mL
- Buffer
- Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- 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
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- TRAPPC2 (Trafficking Protein Particle Complex 2 (TRAPPC2))
- Alternative Name
- TRAPPC2 (TRAPPC2 Products)
- Synonyms
- MIP2A antibody, SEDL antibody, SEDT antibody, TRAPPC2P1 antibody, TRS20 antibody, ZNF547L antibody, hYP38334 antibody, 1110066L09Rik antibody, 1810064C02Rik antibody, AW496358 antibody, MIP-2A antibody, Sedl antibody, RGD1306925 antibody, trafficking protein particle complex 2 antibody, trafficking protein particle complex 2 S homeolog antibody, trappc2 antibody, TRAPPC2 antibody, Trappc2 antibody, trappc2.S antibody
- Background
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Synonyms: hYP38334,MBP 1 interacting protein 2A,MBP-1-interacting protein 2A,MIP 2A,MIP-2A,MIP2A,SEDL,Sedlin,SEDLP,SEDT,Spondyloepiphyseal dysplasia tarda protein,Spondyloepiphyseal dysplasia, late,TPPC2,Trafficking protein particle complex 2,Trafficking protein particle complex subunit 2,TRAPPC2P1,TRS20,ZNF547L
Background: The protein encoded by this gene is thought to be part of a large multi-subunit complex involved in the targeting and fusion of endoplasmic reticulum-to-Golgi transport vesicles with their acceptor compartment. In addition, the encoded protein can bind c-myc promoter-binding protein 1 and block its transcriptional repression capability. Mutations in this gene are a cause of spondyloepiphyseal dysplasia tarda (SEDT). A processed pseudogene of this gene is located on chromosome 19, and other pseudogenes are found on chromosomes 8 and Y. Alternatively spliced transcript variants have been found for this gene.
- Molecular Weight
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Observed_MW: 16kDa
Calculated_MW: 14kDa/16kDa/20kDa
- Gene ID
- 6399
- UniProt
- P0DI81
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