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AV39742

Sigma-Aldrich

Anti-CPXCR1 antibody produced in rabbit

IgG fraction of antiserum

Synonym(s):

Anti-CPX chromosome region, candidate 1

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41

biological source

rabbit

Quality Level

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

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.

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.

Sequence

Synthetic peptide located within the following region: SDTAGNAHKNSENEPPNDCSTDIESPSADPNMIYQVETNPINREPGTATS

Physical form

Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.

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 Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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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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