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Mouse Anti-MAATS1 Recombinant Antibody (CBXC-3013) (CBMAB-C5478-CQ)

This product is a mouse antibody that recognizes MAATS1. The antibody CBXC-3013 can be used for immunoassay techniques such as: WB, IHC.
See all MAATS1 antibodies

Summary

Host Animal
Mouse
Specificity
Human
Clone
CBXC-3013
Antibody Isotype
IgG1
Application
WB, IHC

Basic Information

Immunogen
Recombinant protein corresponding to amino acids 1-313 of human C3orf15 (NP_203528) produced in E. coli
Specificity
Human
Antibody Isotype
IgG1
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

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

Format
Liquid
Buffer
PBS, pH 7.3, 1% BSA, 50% glycerol
Preservative
0.02% sodium azide
Concentration
1 mg/mL
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
MYCBP Associated And Testis Expressed 1
Introduction
MAATS1 (MYCBP Associated And Testis Expressed 1) is a Protein Coding gene. Gene Ontology (GO) annotations related to this gene include adenosylmethionine decarboxylase activity.
Entrez Gene ID
89876
UniProt ID
Q7Z4T9
Alternative Names
MYCBP Associated And Testis Expressed 1; AMY-1-Associating Protein Expressed In Testis 1; MYCBP/AMY-1-Associated Testis-Expressed Protein 1; MYCBP/AMY-1-Associated, Testis Expressed 1; MYCBP-Associated, Testis Expressed 1; Spermatogenesis Associated 26; MYCBP-Binding Protein; Protein MAATS1; C3orf15; CFAP91;
Function
Involved in sperm flagellum axonemal organization and function (PubMed:12223483, PubMed:32161152).
May regulate cilium motility through its role in the assembly of the axonemal radial spokes (By similarity).
Biological Process
Axonemal central apparatus assemblyManual Assertion Based On ExperimentIMP:UniProtKB
Cilium movementISS:UniProtKB
SpermatogenesisManual Assertion Based On ExperimentIMP:UniProtKB
Cellular Location
Mitochondrion
Cytoplasm
Cytoplasm, cytoskeleton, cilium axoneme
Localized in the neck of the sperm.
Isoform 7:
Cytoplasm
Involvement in disease
Spermatogenic failure 51 (SPGF51):
An autosomal recessive infertility disorder characterized by asthenoteratozoospermia. Spermatozoa exhibit multiple morphologic abnormalities, including absent, short, bent, coiled and irregular-caliber flagella. Abnormalities of the sperm head, base, and acrosome have also been observed.
PTM
Phosphorylated by PKA.
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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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