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Kallmann Syndrome 1 Sequence (KAL1) ELISA Kits

Mutations in KAL1 cause the X-linked Kallmann syndrome. Additionally we are shipping KAL1 Antibodies (60) and KAL1 Proteins (2) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
KAL1 3730 P23352
KAL1 171059  
KAL1    
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Top KAL1 ELISA Kits at antibodies-online.com

Showing 4 out of 7 products:

Catalog No. Reactivity Sensitivity Range Quantity Supplier Delivery Price Details
Human 31.25 pg/mL 125-8000 pg/mL 96 Tests Log in to see 11 to 13 Days
$910.56
Details
Chicken
96 Tests Log in to see 11 to 13 Days
$1,095.60
Details
Mouse
96 Tests Log in to see 16 to 21 Days
$999.43
Details
Rat
96 Tests Log in to see 16 to 21 Days
$999.43
Details

Top referenced KAL1 ELISA Kits

  1. Human KAL1 ELISA Kit for Sandwich ELISA - ABIN816739 : Kanda, Shimizu, Fujii, Sueoka, Tanaka, Ezaka, Takami, Tanaka, Hashimoto, Iwata, Kobayashi, Tanaka, Yamada, Nakayama, Sugimoto, Koike, Fujiwara, Kodera: Function and diagnostic value of Anosmin-1 in gastric cancer progression. in International journal of cancer. Journal international du cancer 2015 (PubMed)

More ELISA Kits for KAL1 Interaction Partners

Human Kallmann Syndrome 1 Sequence (KAL1) interaction partners

  1. two novel variants, KAL1 (c.146G>T (p.Cys49Phe)) and mitochondrial tRNAcys (m.5800A>G), were identified in a large Han Chinese family with inherited Kallmann syndrome; although two variants can't exert obvious effects on the migration of GnRH neurons, they show a synergistic effect, which can account for the occurrence of the disorder in this family

  2. FGF receptor 1-mediated anosmin-1 activity plays a crucial role in the continuous remodelling of the adult olfactory bulb.

  3. Study reports 2 new mutations in KAL1 gene from patients with septo-optic dysplasia proven to be loss-of-function.

  4. data indicated KAL1 plays potential suppressive role on OSCC initiation and progression. KAL1 gene may serve as adjuvant biomarker for identification of pathological grade.

  5. Kallmann syndrome with FGFR1 (show FGFR1 ELISA Kits) and KAL1 mutations was detected during fetal life

  6. Our analyses show that the two phenotypes in our patient are due to independent genetic defects: a genomic rearrangement involving the KAL1 gene and a point mutation of the steryl-sulfatase (show STS ELISA Kits) gene.

  7. Results indicated that KAL1 may act as a putative tumor suppressor in hepatocellular carcinoma (HCC (show FAM126A ELISA Kits)) and is inactivated by promoter hypermethylation. KAL1 may serve as a biomarker of malignant phenotype of HCC (show FAM126A ELISA Kits).

  8. No abnormalities were found in the patient group for the PROKR2 (show PROKR2 ELISA Kits) and GNRH1genes. In addition, no genomic rearrangements were identified in the healthy control individuals for the described genes

  9. Mutations were found in the following genes in one or more patients with congenital hypogonadotropic hypogonadism: KAL1, FGFR1 (show FGFR1 ELISA Kits), GNRHR (show GNRHR ELISA Kits), and CHD7 (show CHD7 ELISA Kits)

  10. anosmin-1 has been identified in other pathological scenarios both within (multiple sclerosis) and outside (cancer, atopic dermatitis) the central nerve system.

KAL1 Antigen Profile

Antigen Summary

Mutations in this gene cause the X-linked Kallmann syndrome. The encoded protein is similar in sequence to proteins known to function in neural cell adhesion and axonal migration. In addition, this cell surface protein is N-glycosylated and may have anti-protease activity.

Gene names and symbols associated with KAL1

  • Kallmann syndrome 1 sequence (KAL1) antibody
  • Kallmann syndrome 1 sequence (kal1) antibody
  • Kallmann syndrome 1 sequence (LOC100218922) antibody
  • WAP four-disulfide core domain 18 (Wfdc18) antibody
  • ADMLX antibody
  • Expi antibody
  • HH1 antibody
  • HHA antibody
  • KAL antibody
  • Kal1 antibody
  • KALIG-1 antibody
  • KMS antibody
  • WDNM1 antibody
  • WFDC19 antibody

Protein level used designations for KAL1

Kallmann syndrome 1 sequence , anosmin-1-like , Kallmann syndrome interval gene 1 , Kallmann syndrome-1 sequence (anosmin-1) , WAP four-disulfide core domain 19 , adhesion molecule-like X-linked , anosmin-1 , kallmann syndrome protein , kallmann syndrome protein homolog , WAP four-disulfide core domain protein 18 , extracellular peptidase inhibitor , extracellular proteinase inhibitor

GENE ID SPECIES
465480 Pan troglodytes
100135017 Xenopus (Silurana) tropicalis
100218922 Taeniopygia guttata
100392667 Callithrix jacchus
100440682 Pongo abelii
100559252 Anolis carolinensis
100604302 Nomascus leucogenys
3730 Homo sapiens
396395 Gallus gallus
610921 Canis lupus familiaris
100154011 Sus scrofa
171059 Rattus norvegicus
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