Code
OSA00171W
$240USD
ID Tag
Rb1773-290412-WS
Immunogen
A synthetic peptide from extracellular domain (aa region of 580-680) of human Anoctamin 5 conjugated to blue carrier protein was used as the antigen.
Accession
Also known
Gnathodiaphyseal dysplasia 1 protein, Transmembrane protein 16E, ANO5, GDD1, TMEM16E
Target
FUNCTION: May act as a calcium-activated chloride channel.
Defects in ANO5 are the cause of gnathodiaphyseal dysplasia (GDD).
Defects in ANO5 are the cause of limb-girdle muscular dystrophy type 2L (LGMD2L).
Defects in ANO5 are the cause of miyoshi muscular dystrophy type 3 (MMD3).
Subcellular location: Endoplasmic reticulum membrane; Multi-pass membrane protein.
Tissue specificity: Highly expressed in brain, heart, kidney, lung, and skeletal muscle. Weakly expressed in bone marrow, fetal liver, placenta, spleen, thymus, osteoblasts and periodontal ligament cells.
Storage
Maintain the lyophilised/reconstituted antibodies frozen at -20C for long term storage and refrigerated at 2-8C for a shorter term. When reconstituting, glycerol (1:1) may be added for an additional stability. Avoid freeze and thaw cycles.
Expiry Date
12 months after reconstitution
Shipping
This item will be shipped to you at ambient temperature in a lyophilised form.
References
1. Tsutsumi S, et al. Am. J. Hum. Genet. 74:1255-1261(2004)
Limitation
For research use only
Code
OSA00171W
$240USD
Unit size
100 ul
Conjugate
Unconjugated antibody
Host
NZ white rabbit
Purity
Whole serum
Clonality
Polyclonal
Isotype
Polyclonal, whole serum
Applications
IHC, WB (confirmed by recombinant protein). A dilution of 1 : 300 to 1 : 2000 is recommended. The optimal dilution should be determined by the end user. Not yet tested in other applications.
Specificity
Specific for Anoctamin 5.
Spcs X-react.
Human. Other species not yet tested.
Format
Lyophilised
Reconstitution
Reconstitute in 100 ul of sterile water. Centrifuge to remove any insoluble material.