CLIP2 monoclonal antibody (M07), clone 3H5
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More Files
- More Functions
Western Blot (Transfected lysate)
Western Blot analysis of CLIP2 expression in transfected 293T cell line by CLIP2 monoclonal antibody (M07), clone 3H5.
Lane 1: CLIP2 transfected lysate (Predicted MW: 115.06 KDa).
Lane 2: Non-transfected lysate.
Western Blot detection against Immunogen (36.85 KDa) .
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Specification
Product Description
Mouse monoclonal antibody raised against a partial recombinant CLIP2.
Immunogen
CLIP2 (NP_003379, 946 a.a. ~ 1046 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Sequence
LKDDIRGLREKLTGLDKEKSLSDQRRYSLIDRSSAPELLRLQHQLMSTEDALRDALDQAQQVEKLMEAMRSCPDKAQTIGNSGSANGIHQQDKAQKQEDKH
Host
Mouse
Reactivity
Human
Interspecies Antigen Sequence
Mouse (83)
Isotype
IgG2a Kappa
Quality Control Testing
Antibody Reactive Against Recombinant Protein.
Western Blot detection against Immunogen (36.85 KDa) .
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Transfected lysate)
Western Blot analysis of CLIP2 expression in transfected 293T cell line by CLIP2 monoclonal antibody (M07), clone 3H5.
Lane 1: CLIP2 transfected lysate (Predicted MW: 115.06 KDa).
Lane 2: Non-transfected lysate.
Western Blot (Recombinant protein)
ELISA
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Gene Info — CLIP2
Entrez GeneID
7461GeneBank Accession#
NM_003388Protein Accession#
NP_003379Gene Name
CLIP2
Gene Alias
CLIP, CLIP-115, CYLN2, KIAA0291, MGC11333, WBSCR3, WBSCR4, WSCR3, WSCR4
Gene Description
CAP-GLY domain containing linker protein 2
Omim ID
603432Gene Ontology
HyperlinkGene Summary
The protein encoded by this gene belongs to the family of cytoplasmic linker proteins, which have been proposed to mediate the interaction between specific membranous organelles and microtubules. This protein was found to associate with both microtubules and an organelle called the dendritic lamellar body. This gene is hemizygously deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq
Other Designations
OTTHUMP00000160724|Williams-Beuren syndrome chromosome region 3|Williams-Beuren syndrome chromosome region 4|cytoplasmic linker 2
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Interactome
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Disease
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