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RHOXF2B Antibodies

AND RHOXF2B ELISA kits, RHOXF2B Proteins

Many biological assays use antibodies to detect RHOXF2B, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with RHOXF2B in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop RHOXF2B antibodies...

We validate the specificity of these antibodies to RHOXF2B by testing them on tissues known to express RHOXF2B positively and negatively. Browse below to find the RHOXF2B antibody that suites your experiment. We have 0 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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RHOXF2B Infographic by Boster Bio

RHOXF2B protein infographic

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RHOXF2B Overview

Facts about Rhox homeobox family member 2B.

RHOXF2B 3D structure

RHOXF2B 3D structure. Source: alphafold

Rhox homeobox family member 2B (RHOXF2B)

Transcription factor maybe involved in reproductive processes. Modulates expression of target genes encoding proteins involved in processes relevant to spermatogenesis.

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Gene Information

Human
Gene Name:	RHOXF2B
Uniprot:	P0C7M4
Entrez:	727940

Gene Information

Family

Belongs to:

paired-like homeobox family

Family

Alternative Names

Rhox homeobox family member 2B

Molecular Weight

Mass (kDA):
31.637 kDA

Molecular Weight

Genomic Context


Human

Location:	Xq24
Sequence:	X; NC_000023.11 (120072264..120077690, complement)

Tissue Specificity

Expressed in testis, mainly expressed in germ cells, but also detected in somatic cells such as Sertoli cells, Leydig cells and peritubular cells.

Subcellular Localizations

Nucleus.

Subcellular Localization

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For details, visit:
bosterbio.com/bosterbio-gene-info-cards/RHOXF2B

References

PMID: 28171660 by Borgmann J., et al. The human RHOX gene cluster: target genes and functional analysis of gene variants in infertile men.