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About This Item
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
polyclonal
Application:
WB
Citations:
3
biological source
rabbit
conjugate
unconjugated
antibody form
IgG fraction of antiserum
antibody product type
primary antibodies
clone
polyclonal
form
buffered aqueous solution
mol wt
34 kDa
species reactivity
pig, human, rat, bovine, mouse
concentration
0.5 mg - 1 mg/mL
technique(s)
western blot: suitable
NCBI accession no.
UniProt accession no.
shipped in
wet ice
storage temp.
−20°C
target post-translational modification
unmodified
Gene Information
human ... LZTFL1(54585)
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General description
Leucine zipper transcription factor-like 1 (LZTFL1) is a cytoplasmic protein that interacts with Bardet-Biedl Syndrome (BBS) proteins and regulates their ciliary trafficking. Mutations in this leucine zipper gene have been linked to mesoxial polydactyly in BBS patients. It is also involved in the attenuation of cognitive impairment.
Rabbit Anti-LZTFL1 antibody recognizes human, mouse, rat, canine, zebrafish, and bovine LZTFL1.
Rabbit Anti-LZTFL1 antibody recognizes human, mouse, rat, canine, zebrafish, and bovine LZTFL1.
Immunogen
Synthetic peptide directed towards the C terminal region of human LZTFL1
Application
Rabbit Anti-LZTFL1 antibody is suitable for western blot applications at a concentration of 2.5 μg/ml.
Physical form
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Other Notes
Synthetic peptide located within the following region: VQEQLHMAEKELEKKFQQTAAYRNMKEILTKKNDQIKDLRKRLAQYEPED
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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Storage Class
12 - Non Combustible Liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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E Schaefer et al.
Clinical genetics, 85(5), 476-481 (2013-05-23)
Ciliopathies are heterogeneous disorders sharing different clinical signs due to a defect at the level of the primary cilia/centrosome complex. Postaxial polydactyly is frequently reported in ciliopathies, especially in Bardet-Biedl syndrome (BBS). Clinical features and genetic results observed in a
Takuya Sakurai et al.
Biochemical and biophysical research communications, 416(1-2), 125-129 (2011-11-19)
It is well known that exercise prevents and reduces cognitive impairment. In the present study, we focused on exercise training as a tool to prevent cognitive impairment, and searched for novel molecules that may relate to the prevention of cognitive
Seongjin Seo et al.
PLoS genetics, 7(11), e1002358-e1002358 (2011-11-11)
Many signaling proteins including G protein-coupled receptors localize to primary cilia, regulating cellular processes including differentiation, proliferation, organogenesis, and tumorigenesis. Bardet-Biedl Syndrome (BBS) proteins are involved in maintaining ciliary function by mediating protein trafficking to the cilia. However, the mechanisms
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