Description
Antibody Name: | CLIP2 Antibody (PACO06358) |
Antibody SKU: | PACO06358 |
Size: | 50ug |
Host Species: | Rabbit |
Tested Applications: | ELISA, WB |
Recommended Dilutions: | ELISA:1:5000, WB:1:500-1:2000 |
Species Reactivity: | Human, Mouse, Rat |
Immunogen: | Synthesized peptide derived from the C-terminal region of human CLIP-115. |
Form: | Liquid |
Storage Buffer: | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
Purification Method: | The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. |
Clonality: | Polyclonal |
Isotype: | IgG |
Conjugate: | Non-conjugated |
![]() | Western Blot analysis of NIH-3T3 LOVO cells using CLIP-115 Polyclonal Antibody. |
![]() | Western Blot analysis of A549 cells using CLIP-115 Polyclonal Antibody. |
Synonyms: | CLIP2; CYLN2; KIAA0291; WBSCR3; WBSCR4; WSCR4; CAP-Gly domain-containing linker protein 2; Cytoplasmic linker protein 115; CLIP-115; Cytoplasmic linker protein 2; Williams-Beuren syndrome chromosomal region 3 protein; Williams-Beuren syndro |
UniProt Protein Function: | CYLN2: Seems to link microtubules to dendritic lamellar body (DLB), a membranous organelle predominantly present in bulbous dendritic appendages of neurons linked by dendrodendritic gap junctions. May operate in the control of brain-specific organelle translocations. CLIP2 is located in the Williams-Beuren syndrome (WBS) critical region. WBS results from a hemizygous deletion of several genes on chromosome 7q11.23, thought to arise as a consequence of unequal crossing over between highly homologous low-copy repeat sequences flanking the deleted region. Haploinsufficiency of CLIP2 may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in the disease. 2 isoforms of the human protein are produced by alternative splicing.Protein type: Motility/polarity/chemotaxis; CytoskeletalChromosomal Location of Human Ortholog: 7q11.23Cellular Component: microtubule associated complex |
UniProt Protein Details: | |
NCBI 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, Jul 2008] |
UniProt Code: | Q9UDT6 |
NCBI GenInfo Identifier: | 74753268 |
NCBI Gene ID: | 7461 |
NCBI Accession: | Q9UDT6.1 |
UniProt Secondary Accession: | Q9UDT6,O14527, O43611 |
UniProt Related Accession: | Q9UDT6 |
Molecular Weight: | 111,782 Da |
NCBI Full Name: | CAP-Gly domain-containing linker protein 2 |
NCBI Synonym Full Names: | CAP-Gly domain containing linker protein 2 |
NCBI Official Symbol: | CLIP2 |
NCBI Official Synonym Symbols: | CLIP; CYLN2; WSCR3; WSCR4; WBSCR3; WBSCR4; CLIP-115 |
NCBI Protein Information: | CAP-Gly domain-containing linker protein 2 |
UniProt Protein Name: | CAP-Gly domain-containing linker protein 2 |
UniProt Synonym Protein Names: | Cytoplasmic linker protein 115; CLIP-115; Cytoplasmic linker protein 2; Williams-Beuren syndrome chromosomal region 3 protein; Williams-Beuren syndrome chromosomal region 4 protein |
Protein Family: | CAP-Gly domain-containing linker protein |
UniProt Gene Name: | CLIP2 |
UniProt Entry Name: | CLIP2_HUMAN |