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Mouse Anti-DAZ1 Recombinant Antibody (3G10) (CBMAB-D0270-YC)

Provided herein is a Mouse monoclonal antibody, which binds to Deleted In Azoospermia 1 (DAZ1). The antibody can be used for immunoassay techniques, such as ELISA, WB, IHC, IF.
See all DAZ1 antibodies

Summary

Host Animal
Mouse
Specificity
Human
Clone
3G10
Antibody Isotype
IgG1, κ
Application
ELISA, WB, IHC, IF

Basic Information

Immunogen
DAZ1 (-, 21 a.a. ~ 121 a.a) partial recombinant protein with GST tag.
Specificity
Human
Antibody Isotype
IgG1, κ
Clonality
Monoclonal
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!]

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
deleted in azoospermia 1
Introduction
DAZ1 is a member of the DAZ gene family and is a candidate for the human Y-chromosomal azoospermia factor (AZF). Its expression is restricted to premeiotic germ cells, particularly in spermatogonia. It encodes an RNA-binding protein that is important for spermatogenesis.
Entrez Gene ID
1617
UniProt ID
Q9NQZ3
Alternative Names
Deleted In Azoospermia 1; SPGY; DAZ; Deleted In Azoospermia Protein 1; Testicular Tissue Protein Li 49; Deleted In Azoospermia;
Function
RNA-binding protein that plays an essential role in spermatogenesis. May act by binding to the 3'-UTR of mRNAs and regulating their translation. Promotes germ-cell progression to meiosis and formation of haploid germ cells.
Biological Process
3'-UTR-mediated mRNA stabilization Source: GO_Central
Cell differentiation Source: UniProtKB-KW
Multicellular organism development Source: UniProtKB-KW
Positive regulation of translational initiation Source: UniProtKB
Spermatogenesis Source: UniProtKB-KW
Cellular Location
Nucleus; Cytoplasm. Predominantly cytoplasmic. Nuclear at some stages of spermatozoide development. Localizes both to the nuclei and cytoplasm of spermatozoide differentiation. Nuclear in fetal gonocytes and in spermatogonial nuclei. It then relocates to the cytoplasm during male meiosis.
Involvement in disease
Spermatogenic failure Y-linked 2 (SPGFY2):
The disease may be caused by variants affecting the gene represented in this entry. AZFc deletions in the Yq11.23 region including the DAZ genes are the most common known genetic cause of human male infertility. A disorder resulting in the absence (azoospermia) or reduction (oligozoospermia) of sperm in the semen, leading to male infertility.
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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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