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Rabbit anti-Human SLC35C1 Polyclonal Antibody | anti-SLC35C1 antibody

SLC35C1 Antibody, Biotin conjugated

Gene Names
SLC35C1; CDG2C; FUCT1
Reactivity
Human
Applications
ELISA
Purity
>95%, Protein G Purified
Synonyms
SLC35C1; Polyclonal Antibody; SLC35C1 Antibody; Biotin conjugated; GDP-fucose transporter 1; FUCT1; Solute carrier family 35 member C1; anti-SLC35C1 antibody
Ordering
For Research Use Only!
Host
Rabbit
Reactivity
Human
Clonality
Polyclonal
Isotype
IgG
Purity/Purification
>95%, Protein G Purified
Sequence Length
351
Applicable Applications for anti-SLC35C1 antibody
ELISA (EIA)
Storage Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
Conjugate
Biotin
Immunogen
Recombinant human GDP-fucose transporter 1 protein
Santa Cruz Alternative
Potential replacement for Santa Cruz Biotechnology antibody catalog# sc-132832 / sc-102113
Preparation and Storage
Shipped at 4 degree C. Upon delivery aliquot and store at -20 degree C or -80 degree C. Avoid repeated freeze.
Related Product Information for anti-SLC35C1 antibody
Involved in GDP-fucose import from the cytoplasm into the Golgi lumen.

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Accession #
Molecular Weight
38,235 Da
NCBI Official Full Name
GDP-fucose transporter 1 isoform b
NCBI Official Synonym Full Names
solute carrier family 35 (GDP-fucose transporter), member C1
NCBI Official Symbol
SLC35C1
NCBI Official Synonym Symbols
CDG2C; FUCT1
NCBI Protein Information
GDP-fucose transporter 1
UniProt Protein Name
GDP-fucose transporter 1
UniProt Gene Name
SLC35C1
UniProt Synonym Gene Names
FUCT1
UniProt Entry Name
FUCT1_HUMAN

NCBI Description

This gene encodes a GDP-fucose transporter that is found in the Golgi apparatus. Mutations in this gene result in congenital disorder of glycosylation type IIc. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009]

Uniprot Description

SLC35C1: Involved in GDP-fucose import from the cytoplasm into the Golgi lumen. Defects in SLC35C1 are the cause of congenital disorder of glycosylation type 2C (CDG2C); also known as leukocyte adhesion deficiency type II (LAD2). CDGs are a family of severe inherited diseases caused by a defect in protein N- glycosylation. They are characterized by under-glycosylated serum proteins. These multisystem disorders present with a wide variety of clinical features, such as disorders of the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions. The clinical features of CDG2C include mental retardation, short stature, facial stigmata, and recurrent bacterial peripheral infections with persistently elevated peripheral leukocytes. Biochemically, CDG2C is characterized by a lack of fucosylated glycoconjugates, including selectin ligands. Belongs to the TPT transporter family. SLC35C subfamily.

Protein type: Transporter; Transporter, SLC family; Membrane protein, integral; Membrane protein, multi-pass

Chromosomal Location of Human Ortholog: 11p11.2

Cellular Component: Golgi apparatus; Golgi membrane; integral to membrane

Biological Process: carbohydrate transport; cellular protein metabolic process; dolichol-linked oligosaccharide biosynthetic process; lipid glycosylation; negative regulation of Notch signaling pathway; positive regulation of defense response to virus by host; post-translational protein modification; protein amino acid N-linked glycosylation via asparagine; transmembrane transport

Disease: Congenital Disorder Of Glycosylation, Type Iic

Research Articles on SLC35C1

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Product Notes

The SLC35C1 slc35c1 (Catalog #AAA1498207) is an Antibody produced from Rabbit and is intended for research purposes only. The product is available for immediate purchase. The SLC35C1 Antibody, Biotin conjugated reacts with Human and may cross-react with other species as described in the data sheet. AAA Biotech's SLC35C1 can be used in a range of immunoassay formats including, but not limited to, ELISA (EIA). Researchers should empirically determine the suitability of the SLC35C1 slc35c1 for an application not listed in the data sheet. Researchers commonly develop new applications and it is an integral, important part of the investigative research process. It is sometimes possible for the material contained within the vial of "SLC35C1, Polyclonal Antibody" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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