AV39742
Anti-CPXCR1 antibody produced in rabbit
IgG fraction of antiserum
别名:
Anti-CPX chromosome region, candidate 1
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关于此项目
NACRES:
NA.41
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
polyclonal
Application:
WB
Citations:
1
biological source
rabbit
conjugate
unconjugated
antibody form
IgG fraction of antiserum
antibody product type
primary antibodies
clone
polyclonal
form
buffered aqueous solution
mol wt
35 kDa
species reactivity
human
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
Quality Level
Gene Information
human ... CPXCR1(53336)
General description
CPXCR1 is a candidate gene in the CPX chromosome region and is widely expressed in fetal tissues.
Rabbit Anti-CPXCR1 antibody recognizes human CPXCR1.
Rabbit Anti-CPXCR1 antibody recognizes human CPXCR1.
Immunogen
Synthetic peptide directed towards the N terminal region of human CPXCR1
Application
Rabbit Anti-CPXCR1 antibody is suitable for western blot applications at a concentration of 1.25 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: SDTAGNAHKNSENEPPNDCSTDIESPSADPNMIYQVETNPINREPGTATS
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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存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
C Braybrook et al.
Human genetics, 108(6), 537-545 (2001-08-14)
Cleft palate most commonly occurs as a sporadic multifactorial disorder with a clear but difficult to define genetic component. As a semi-dominant disorder, X-linked cleft palate (CPX) provides a useful model to investigate a congenital defect that is little influenced
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