Thermo Fisher Scientific CCDC22 Polyclonal Antibody
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Applications
Tested Dilution
Publications
Western Blot (WB)
0.04-0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC (P))
1:500-1:1,000
Immunocytochemistry (ICC/IF)
0.25-2 µg/mL
Product Specifications
Species Reactivity
Human, Mouse, Rat
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant protein corresponding to Human CCDC22. Recombinant protein control fragment (Product #RP-91924). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
CCDC22,
uniProtId:
O60826-1,
ncbiNodeId:
9606,
antigenRange:
86-204,
antigenLength:
627,
antigenImageFileName:
PA5-51477_CCDC22_O60826-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-51477_CCDC22_O60826-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.3 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
PBS, pH 7.2, with 40% glycerol
Contains
0.02% sodium azide
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Wet ice
RRID
AB_2639440
Product Specific Information
Immunogen sequence: YQNFLYPSEP DLRDLLLFLA ERLPTDASED ADQPAGDSAI LLRAIGSQIR DQLALPWVPP HLRTPKLQHL QGSALQKPFH ASRLVVPELS SRGEPREFQA SPLLLPVPTQ VPQPVGRVA
Highest antigen sequence identity to the following orthologs: Mouse - 87%, Rat - 87%.
Target Information
CCDC22 is a recently identified coiled-coil domain-containing protein that has been shown to bind copines, which are calcium-dependent, membrane-binding proteins that may function in calcium signaling. In rat, CCDC22 has been observed to localize in multiple regions of the brain, including the prefrontal and somatosensory cortex, dentate gyrus and thalamus, and in the ipsilateral motor neurons of the spinal cord after sciatic nerve transection suggesting that it may play a role in neuronal injury response. The human CCDC22 gene has been identified as a novel candidate gene for syndromic X-linked intellectual disability (XLID).
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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