NME8 Antibody

Code CSB-PA889073
Size US$166
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Image
  • The image on the left is immunohistochemistry of paraffin-embedded Human liver cancer tissue using CSB-PA889073(NME8 Antibody) at dilution 1/25, on the right is treated with fusion protein. (Original magnification: ×200)
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Product Details

Uniprot No.
Target Names
NME8
Alternative Names
NME8 antibody; SPTRX2 antibody; TXNDC3 antibody; Thioredoxin domain-containing protein 3 antibody; NM23-H8 antibody; NME/NM23 family member 8 antibody; Spermatid-specific thioredoxin-2 antibody; Sptrx-2 antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Fusion protein of Human NME8
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Isotype
IgG
Purification Method
Antigen affinity purification
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
Form
Liquid
Tested Applications
ELISA,IHC
Recommended Dilution
Application Recommended Dilution
ELISA 1:2000-1:5000
IHC 1:25-1:100
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Function
Probably required during the final stages of sperm tail maturation in the testis and/or epididymis, where extensive disulfide bonding of fibrous sheath (FS) proteins occurs. May be involved in the reduction of disulfide bonds within the sperm FS components. In vitro, it has neither NDP kinase nor reducing activity on disulfide bonds.
Gene References into Functions
  1. Studies suggest that the rs2718058 near gene NME8 on chromosome 7p14.1 might not play a major role in the genetic predisposition to late-onset Alzheimer's disease (LOAD) in the North Han Chinese. PMID: 27144521
  2. Addition of the minor allele for rs670139 (MS4A4E), rs9331896 (CLU), and rs12155159 (NME8) was nominally associated with change on the DWRT, DSST, and WFT, respectively, in whites. PMID: 27781389
  3. NME8 locus polymorphism is associated with cognitive decline, cerebrospinal fluid and neuroimaging biomarkers in Alzheimer's disease. PMID: 25486118
  4. GPR141-NME8 locus had strong genetic effect on the susceptibility to generalized periodontitis in Japanese individuals with history of smoking. identified 2 suggestive loci for periodontitis in a Japanese population. PMID: 25672891
  5. Our approach yielded 26 candidate genes differentially expressed between patients (Osteoarthritis) and controls. The presence of allelic imbalances confirms cis-regulatory mechanisms for RHOB and TXNDC3. PMID: 16642435
  6. genetic association of RHOB and TXNDC3 with osteoarthritis was detected PMID: 17304710
  7. Primary ciliary dyskinesia is caused by an SNP-induced modification of the ratio of two physiological isoforms of TXNDC3 generated by alternative splicing. PMID: 17360648
  8. The minor allele frequencies of TXNDC3 in East Asian individuals are significantly different from those in United Kingdom control individuals. PMID: 18471322

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Involvement in disease
Ciliary dyskinesia, primary, 6 (CILD6)
Subcellular Location
Cytoplasm.
Protein Families
NDK family
Tissue Specificity
Testis-specific. Expressed only in primary spermatocytes and round spermatids.
Database Links

HGNC: 16473

OMIM: 607421

KEGG: hsa:51314

STRING: 9606.ENSP00000199447

UniGene: Hs.723454

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