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Mouse Anti-SEMA3A Recombinant Antibody (CBT3595) (V2LY-0625-LY182)

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Tested Data

Summary

Host Animal
Mouse
Specificity
Human
Clone
CBT3595
Antibody Isotype
IgG1
Application
FC

Basic Information

Immunogen
Synthesized peptide of human SEMAPHORIN-3A (AA: 359-372).
Host Species
Mouse
Specificity
Human
Antibody Isotype
IgG1
Clonality
Monoclonal Antibody
Application Notes
ApplicationNote
FC1:200-1:400
ELISA1:10,000

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
PBS
Preservative
Sodium azide
Concentration
Batch dependent
Purity
> 95% Purity determined by SDS-PAGE.
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.

Target

Entrez Gene ID
Function
Involved in the development of the olfactory system and in neuronal control of puberty. Induces the collapse and paralysis of neuronal growth cones. Could serve as a ligand that guides specific growth cones by a motility-inhibiting mechanism. Binds to the complex neuropilin-1/plexin-1.
Biological Process
Biological Process apoptotic processIEA:Ensembl
Biological Process axon extension involved in axon guidanceISS:BHF-UCL
Biological Process axon guidanceManual Assertion Based On ExperimentIBA:GO_Central
Biological Process axonogenesis involved in innervationISS:BHF-UCL
Biological Process basal dendrite arborizationBy SimilarityISS:ARUK-UCL
Biological Process motor neuron axon guidanceManual Assertion Based On ExperimentIBA:GO_Central
Biological Process negative chemotaxisManual Assertion Based On ExperimentIBA:GO_Central
Biological Process negative regulation of axon extension involved in axon guidanceManual Assertion Based On ExperimentIBA:GO_Central
Biological Process negative regulation of neuron projection developmentManual Assertion Based On ExperimentIMP:ParkinsonsUK-UCL
Biological Process nerve developmentISS:BHF-UCL
Biological Process neural crest cell migrationManual Assertion Based On ExperimentIBA:GO_Central
Biological Process neural crest cell migration involved in autonomic nervous system developmentISS:BHF-UCL
Biological Process neuron migrationISS:BHF-UCL
Biological Process olfactory bulb developmentManual Assertion Based On ExperimentIMP:UniProtKB
Biological Process positive regulation of cell migrationManual Assertion Based On ExperimentIBA:GO_Central
Biological Process positive regulation of JNK cascadeManual Assertion Based On ExperimentTAS:ARUK-UCL
Biological Process positive regulation of neuron migrationManual Assertion Based On ExperimentIBA:GO_Central
Biological Process regulation of axon extension involved in axon guidanceManual Assertion Based On ExperimentIDA:UniProtKB
Biological Process semaphorin-plexin signaling pathwayManual Assertion Based On ExperimentIBA:GO_Central
Biological Process semaphorin-plexin signaling pathway involved in neuron projection guidanceISS:BHF-UCL
Biological Process sensory system developmentManual Assertion Based On ExperimentTAS:BHF-UCL
Biological Process sympathetic ganglion developmentISS:BHF-UCL
Biological Process sympathetic nervous system developmentManual Assertion Based On ExperimentTAS:BHF-UCL
Biological Process sympathetic neuron projection extensionISS:BHF-UCL
Biological Process sympathetic neuron projection guidanceISS:BHF-UCL
Cellular Location
Secreted
Involvement in disease
Hypogonadotropic hypogonadism 16 with or without anosmia (HH16):
A disorder characterized by absent or incomplete sexual maturation by the age of 18 years, in conjunction with low levels of circulating gonadotropins and testosterone and no other abnormalities of the hypothalamic-pituitary axis. In some cases, it is associated with non-reproductive phenotypes, such as anosmia, cleft palate, and sensorineural hearing loss. Anosmia or hyposmia is related to the absence or hypoplasia of the olfactory bulbs and tracts. Hypogonadism is due to deficiency in gonadotropin-releasing hormone and probably results from a failure of embryonic migration of gonadotropin-releasing hormone-synthesizing neurons. In the presence of anosmia, idiopathic hypogonadotropic hypogonadism is referred to as Kallmann syndrome, whereas in the presence of a normal sense of smell, it has been termed normosmic idiopathic hypogonadotropic hypogonadism (nIHH).
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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