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Home Antibody All anti-ALX4 antibodies

Anti-ALX4 TRUEMAB Antibody Clone OTI6B3

TrueMAB™ Antibodies - Made against Authentic Protein Antigens

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Specifications Citations (0) Related Products Product Documents
SKU Description Amount Price Availability*  
TA505173 ALX4 mouse monoclonal antibody, clone OTI6B3 (formerly 6B3) 100ul $379 In Stock
LC411892 ALX4 HEK293T cell transient overexpression lysate (as WB positive control) 20ug $50 In Stock
CF505173 Carrier-free (BSA/glycerol-free) ALX4 mouse monoclonal antibody, clone OTI6B3 (formerly 6B3) 100ug $450 3 Days
Conjugation is available for this antibody: choose conjugation type

Buy any antibody of 100ul or more, get a free package of 3 loading control antibody samples. View Details Add to Shopping Cart

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WB(1)
IHC(2)
IF(1)

OriGene Data

ImmunogenFull length human recombinant protein of human ALX4(NP_068745) produced in HEK293T cell.
Clone NameClone OTI6B3 IsotypeIgG1
Species ReactivityHuman Concentration1 mg/ml
Guaranteed Application *WB, IHC, IF Suggested Dilutions WB 1:2000, IHC 1:150, IF 1:100,
Predicted MW Explanation 44.1 kDa
BufferPBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Purification Purified from mouse ascites fluids by affinity chromatography

Reference Data

Target NameHomo sapiens ALX homeobox 4 (ALX4)
Alternative NameCRS5; FND2
Database LinkNP_068745
Entrez Gene 60529 Human
FunctionThis gene encodes a paired-like homeodomain transcription factor expressed in the mesenchyme of developing bones, limbs, hair, teeth, and mammary tissue. Mutations in this gene cause parietal foramina 2 (PFM2); an autosomal dominant disease characterized by deficient ossification of the parietal bones. Mutations in this gene also cause a form of frontonasal dysplasia with alopecia and hypogonadism; suggesting a role for this gene in craniofacial development, mesenchymal-epithelial communication, and hair follicle development. Deletion of a segment of chromosome 11 containing this gene, del(11)(p11p12), causes Potocki-Shaffer syndrome (PSS); a syndrome characterized by craniofacial anomalies, mental retardation, multiple exostoses, and genital abnormalities in males. In mouse, this gene has been shown to use dual translation initiation sites located 16 codons apart. [provided by RefSeq].
Related PathwayDruggable Genome

* Availability is in business days
* OriGene provides validated application data and protocol, with money back guarantee.

HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY ALX4 (RC224459, Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-ALX4.
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Immunohistochemical staining of paraffin-embedded Human colon tissue within the normal limits using anti-ALX4 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 100C for 10min, TA505173)
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Immunohistochemical staining of paraffin-embedded Adenocarcinoma of Human endometrium tissue using anti-ALX4 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 100C for 10min, TA505173)
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Anti-ALX4 mouse monoclonal antibody (TA505173) immunofluorescent staining of COS7 cells transiently transfected by pCMV6-ENTRY ALX4(RC224459).
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