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anti-Solute Carrier Family 24 (Sodium/potassium/calcium Exchanger), Member 5 (SLC24A5) Antibodies

SLC24A5 is a member of the potassium-dependent sodium/calcium exchanger family and encodes an intracellular membrane protein with 2 large hydrophilic loops and 2 sets of multiple transmembrane-spanning segments.

list all antibodies Gene Name GeneID UniProt
SLC24A5 283652 Q71RS6
Anti-Rat SLC24A5 SLC24A5 311387  
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Top anti-SLC24A5 Antibodies at antibodies-online.com

Showing 7 out of 7 products:

Catalog No. Reactivity Host Conjugate Application Quantity Supplier Delivery Price Details
Human Goat Alkaline Phosphatase (AP) ELISA, WB 100 μL Log in to see 16 Days
$713.43
Details
Human Goat APC ELISA, WB 100 μL Log in to see 16 Days
$713.43
Details
Human Goat Biotin ELISA, WB 100 μL Log in to see 16 Days
$713.43
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Human Goat FITC ELISA, WB 100 μL Log in to see 16 Days
$713.43
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Human Goat PE ELISA, WB 100 μL Log in to see 16 Days
$713.43
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Human Goat Un-conjugated ELISA, WB 100 μg Log in to see 11 to 16 Days
$526.43
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Human Goat HRP ELISA, WB 100 μL Log in to see 16 Days
$713.43
Details

SLC24A5 Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality Conjugate
Human


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More Antibodies against SLC24A5 Interaction Partners

Human Solute Carrier Family 24 (Sodium/potassium/calcium Exchanger), Member 5 (SLC24A5) interaction partners

  1. a novel homozygous mutation in SLC24A5 in two patients from French Guiana strengthens the importance of screening this gene in oculocutaneous albinism patients.

  2. the SLC24A5 gene locus known to be associated with skin pigmentation was in the top selection signals in the Wolaita, and the alleles of single-nucleotide polymorphisms rs1426654 and rs1834640 (SLC24A5) associated with light skin pigmentation

  3. Polymorphisms of SLC24A5 were found to be associated with skin, hair, and eye color in a phenotypically diverse Brazilian population, considered useful in forensic science for crime investigation and facial reconstruction in unknown bodies.

  4. All chromosomes carrying the A111T allele of SLC24A5 gene share a single 78-kb haplotype indicating that all instances of this mutation in human populations share a common origin.

  5. Sequencing 11.74 kb of SLC24A5 in 95 individuals worldwide reveals that the rs1426654-A alleles in South Asian and West Eurasian populations are monophyletic and occur on the background of a common haplotype that is characterized by low genetic diversity

  6. We observed a heterogeneous phenotype among seven oculocutaneous albinism patients with SLC24A5 mutations.

  7. SLC24A5 is a previously unreported nonsyndromic oculocutaneous albinism candidate gene.

  8. NCKX5, a natural regulator of human skin colour variation, regulates the expression of key pigment genes MC1R and alpha-MSH and alters cholesterol homeostasis in normal human melanocytes.

  9. the variant allele is associated with a substantial reduction in regional heterozygosity, and correlates with lighter skin pigmentation in admixed populations, suggesting a key role for the SLC24A5 gene in human pigmentation

  10. The p.L374F allele in SLC45A2 (show SLC45A2 Antibodies) is a more specific ancestry informative marker than the p.A111T allele in SLC24A5, as it clearly distinguishes Sri (show SRI Antibodies) Lankans from Europeans.

Zebrafish Solute Carrier Family 24 (Sodium/potassium/calcium Exchanger), Member 5 (SLC24A5) interaction partners

  1. golden mutants are associated with diminished number, size and density of melanosomes; golden encodes a putative cation exchanger slc24a5 that localizes to an intracellular membrane, likely the melanosome or its precursor

SLC24A5 Antigen Profile

Protein Summary

This gene is a member of the potassium-dependent sodium/calcium exchanger family and encodes an intracellular membrane protein with 2 large hydrophilic loops and 2 sets of multiple transmembrane-spanning segments. Sequence variation in this gene has been associated with differences in skin pigmentation.

Gene names and symbols associated with SLC24A5

  • solute carrier family 24 (sodium/potassium/calcium exchanger), member 5 (SLC24A5) antibody
  • solute carrier family 24 (sodium/potassium/calcium exchanger), member 5 (Slc24a5) antibody
  • solute carrier family 24, member 5 (SLC24A5) antibody
  • solute carrier family 24, member 5 (slc24a5) antibody
  • solute carrier family 24 member 5 (slc24a5) antibody
  • JSX antibody
  • NCKX5 antibody
  • OCA6 antibody
  • SHEP4 antibody
  • slc24a5 antibody

Protein level used designations for SLC24A5

Na(+)/K(+)/Ca(2+)-exchange protein 5 , ion transporter JSX , oculocutaneous albinism 6 (autosomal recessive) , sodium/potassium/calcium exchanger 5 , solute carrier family 24, member 5 , solute carrier family 24 (sodium/potassium/calcium exchanger), member 5 , K-dependent Na,Ca exchanger 5 , gol , gol-1 , golden , golden-1 , protein golden , solute carrier family 24 member 5 , sodium/potassium/calcium exchanger 5-like

GENE ID SPECIES
283652 Homo sapiens
311387 Rattus norvegicus
415431 Gallus gallus
453408 Pan troglodytes
570312 Danio rerio
612878 Canis lupus familiaris
781411 Bos taurus
100031075 Monodelphis domestica
100055828 Equus caballus
100302013 Oryzias latipes
100349943 Oryctolagus cuniculus
100413824 Callithrix jacchus
100457520 Pongo abelii
100477207 Ailuropoda melanoleuca
100511672 Sus scrofa
100550043 Meleagris gallopavo
100603658 Nomascus leucogenys
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