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AB15360

Sigma-Aldrich

Anti-Calcitonin Gene Related Peptide Antibody

serum, Chemicon®

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Synonym(s):
CGRP
eCl@ss:
32160702
NACRES:
NA.41

biological source

rabbit

Quality Level

antibody form

serum

antibody product type

primary antibodies

clone

polyclonal

species reactivity

rat

manufacturer/tradename

Chemicon®

technique(s)

immunohistochemistry: suitable

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Gene Information

human ... CALCA(796)

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AB5705MAB317C8198
biological source

rabbit

biological source

chicken

biological source

mouse

biological source

rabbit

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

200

technique(s)

immunohistochemistry: suitable

technique(s)

immunohistochemistry: suitable

technique(s)

ELISA: suitable, immunohistochemistry: suitable

technique(s)

-

species reactivity

rat

species reactivity

rat

species reactivity

guinea pig, human

species reactivity

rat

shipped in

wet ice

shipped in

dry ice

shipped in

wet ice

shipped in

dry ice

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Specificity

Recognizes Calcitonin Gene Related Peptide (CGRP).

Immunogen

Synthetic calcitonin gene related peptide.

Application

Anti-Calcitonin Gene Related Peptide Antibody detects level of Calcitonin Gene Related Peptide & has been published & validated for use in IH.
Immunohistochemistry on frozen rat spinal cord: 1:2,000-1:4,000 using the Chemicon IHC-Select Kit with HRP-DAB detection system.

Optimal working dilutions must be determined by the end user.
Research Category
Neuroscience
Research Sub Category
CNS Control of Metabolism

Hormones & Receptors

Linkage

Replaces: AB1971

Physical form

Rabbit serum. Liquid.
Serum

Storage and Stability

Maintain at -20°C in undiluted aliquots for up to 12 months after date of receipt. Avoid repeated freeze/thaw cycles.

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

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.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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Andrea M Sartori et al.
Experimental neurology, 348, 113937-113937 (2021-11-27)
Neurogenic lower urinary tract dysfunction typically develops after spinal cord injury. We investigated the time course and the anatomical changes in the spinal cord that may be causing lower urinary tract symptoms following injury. Rats were implanted with a bladder
Andrew H Cooper et al.
Pain reports, 5(6), e872-e872 (2020-12-05)
Inflammation during the neonatal period can exacerbate pain severity following reinjury in adulthood. This is driven by alterations in the postnatal development of spinal and supraspinal nociceptive circuitry. However, the contribution of alterations in peripheral nociceptor function remains underexplored. We
Michał Bulc et al.
Journal of diabetes research, 2018, 4735659-4735659 (2018-08-25)
One of the most frequently reported disorders associated with diabetes is gastrointestinal (GI) disturbance. Although pathogenesis of these complications is multifactorial, the complicity of the enteric nervous system (ENS) in this respect has significant importance. Therefore, this paper analysed changes
A virus-like particle-based anti-nerve growth factor vaccine reduces inflammatory hyperalgesia: potential long-term therapy for chronic pain.
Rohn, TA; Ralvenius, WT; Paul, J; Borter, P; Hernandez, M; Witschi, R; Grest et al.
Journal of immunology (Baltimore, Md. : 1950) (1950)
Devin M Barry et al.
Molecular pain, 12 (2016-04-14)
There are substantial disagreements about the expression of gastrin-releasing peptide (GRP) in sensory neurons and whether GRP antibody cross-reacts with substance P (SP). These concerns necessitate a critical revaluation of GRP expression using additional approaches. Here, we show that a

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