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KNDC1 Polyclonal Antibody, ALEXA FLUOR® 555 Conjugated


  • WB
  • IF(IHC-P)
  • IF(IHC-F)
  • IF(ICC)


  • Others

Predicted Reactivity

  • Human
  • Mouse
  • Rat
  • Pig
  • Chicken
Catalog # bs-10056R-A555
Product Name KNDC1 Polyclonal Antibody, ALEXA FLUOR® 555 Conjugated
Applications WB, IF(IHC-P), IF(IHC-F), IF(ICC)
Reactivity Others
Predicted Reactivity Human, Mouse, Rat, Pig, Chicken
Conjugation ALEXA FLUOR® 555
Host Rabbit
Source KLH conjugated synthetic peptide derived from human KNDC1
Immunogen Range 1601-1749/1749
Clonality Polyclonal
Isotype IgG
Concentration 1ug/ul
Purification Purified by Protein A.
Storage Buffer Aqueous buffered solution containing 0.01M TBS (pH 7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Condition Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
Gene ID 85442
Subcellular location Cytoplasm, Nucleus
Synonyms Cerebral protein 9; FLJ25027; hucep-9; KIAA1768; Kinase non-catalytic C-lobe domain-containing protein 1; KIND domain-containing protein 1; KNDC1; Protein very KIND; Ras-GEF domain-containing family member 2; RASGEF2; VKIND; VKIND_HUMAN; bB439H18.3; C10orf23.
Background KNDC1 is a 1,749 amino acid protein that contains two KIND domains and an N-terminal Ras-GEF domain. Expressed in the cerebral cortex, KNDC1 is a likely guanine nucleotide exchange factor (GEF). Existing as six alternatively spliced isoforms, the gene encoding KNDC1 maps to human chromosome 10q26.3 and mouse chromosome 7 F4. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Application Dilution
WB 1:300-5000
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200