Stearoyl-CoA desaturase 5 Antibodies

AND SCD5 ELISA kits, Stearoyl-CoA desaturase 5 Proteins

Many biological assays use antibodies to detect Stearoyl-CoA desaturase 5, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Stearoyl-CoA desaturase 5 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Stearoyl-CoA desaturase 5 antibodies...

We validate the specificity of these antibodies to Stearoyl-CoA desaturase 5 by testing them on tissues known to express SCD5 positively and negatively. Browse below to find the SCD5 antibody that suites your experiment. We have 1 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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SCD5 Infographic by Boster Bio

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SCD5 (NM_001037582) Human Over-expression Lysate

SCD5 Human Over-expression Lysates NM_001037582

Human

$628
Cat # LS079966
20 µg, 100 µg

SCD5 Overview

Facts about Stearoyl-CoA desaturase 5.

SCD5 3D structure. Source: alphafold

Stearoyl-CoA desaturase 5 (SCD5)

Stearyl-CoA desaturase that utilizes O(2) and electrons from reduced cytochrome b5 to introduce the first double bond to saturated fatty acyl-CoA substrates. Catalyzes the insertion of a cis double bond in the delta-9 place into fatty acyl-CoA substrates including palmitoyl-CoA and stearoyl-CoA (PubMed:15907797, PubMed:15610069).

Gives rise to a mixture of 16:1 and 18:1 unsaturated fatty acids. .

Gene Information

Human
Gene Name:	SCD5
Uniprot:	Q86SK9
Entrez:	79966

Family

Belongs to:

fatty acid desaturase type 1 family

Alternative Names

ACOD4Acyl-CoA-desaturase 4; FADS4; FLJ21032; HSCD5Stearoyl-CoA 9-desaturase; SCD2; SCD4EC 1.14.19.1; stearoyl-CoA desaturase 4; stearoyl-CoA desaturase 5

Molecular Weight

Mass (kDA):
37.61 kDA

Genomic Context


Human

Location:	4q21.22
Sequence:	4; NC_000004.12 (82629539..82798857, complement)

Tissue Specificity

Detected in fetal brain, and at lower levels in fetal kidney. Detected in adult brain and pancreas, and at lower levels in kidney and lung.

Subcellular Localizations

Endoplasmic reticulum membrane; Multi-pass membrane protein.

Diseases

Malignant Neoplasms
Neoplasms
Patient Dependence On
Malignant Neoplasm Of Stomach
Obesity
Nervousness
Depressive Disorder
Malignant Neoplasm Of Breast

Medication Reaction
Endoplasmic Reticulum Stress

Pathways

Endocytosis
Cell Growth
Lactation
Secretory Pathway
Localization
Meiosis
Transport
Receptor-mediated Endocytosis
Actin Cytoskeleton Organization
Cell Proliferation
Induction Of Apoptosis
Dna Repair
Metaphase

Oocyte Maturation
Sporulation
Nuclear Export
Myelination
Cell Division
Drug Resistance
Cytoskeleton Organization

PTMs

Phosphorylation

Glycosylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/SCD5

References

PMID: 12727354 by Beiraghi S., et al. Identification and characterization of a novel gene disrupted by a pericentric inversion inv(4)(p13.1q21.1) in a family with cleft lip.

PMID: 15907797 by Wang J., et al. Characterization of HSCD5, a novel human stearoyl-CoA desaturase unique to primates.