SYNC Antibody, HRP conjugated

Datasheet

Code	CSB-PA862034LB01HU
Size	US$166
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Product Details
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Target Background

Product Details

Full Product Name

Rabbit anti-Homo sapiens (Human) SYNC Polyclonal antibody

Uniprot No.

Q9H7C4

Target Names

SYNC

Alternative Names

1110057H03Rik antibody; Intermediate filament protein syncoilin antibody; MGC124230 antibody; MGC149625 antibody; MGC149626 antibody; RP23-391E6.2 antibody; SNIP4 antibody; SYNC antibody; SYNC1 antibody; SYNCI_HUMAN antibody; Syncoilin antibody; Syncoilin intermediate filament 1 antibody; Syncoilin-1 antibody

Raised in

Rabbit

Species Reactivity

Human

Immunogen

Recombinant Human Syncoilin protein (332-482AA)

Immunogen Species

Homo sapiens (Human)

Conjugate

HRP

Clonality

Polyclonal

Isotype

IgG

Purification Method

>95%, Protein G purified

Concentration

It differs from different batches. Please contact us to confirm it.

Buffer

Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4

Form

Liquid

Tested Applications

ELISA

Protocols

ELISA Protocol

Troubleshooting and FAQs

Antibody FAQs

Storage

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Lead Time

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

Usage

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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Target Background

Function

Atypical type III intermediate filament (IF) protein that may play a supportive role in the efficient coupling of mechanical stress between the myofibril and fiber exterior. May facilitate lateral force transmission during skeletal muscle contraction. Does not form homofilaments nor heterofilaments with other IF proteins.

Gene References into Functions

Syncoilin modulates peripherin filament network formation. PMID: 20587592
The differences in human syncoilin and beta-synemin mRNA ratios between Duchenne muscular dystrophy and normal muscles were not statistically significant PMID: 20199207
the result of this study raise the possibility that mutations in the gene encoding for syncoilin may underlie some forms of muscle disease. PMID: 16124004

Subcellular Location

Cytoplasm, perinuclear region.

Protein Families

Intermediate filament family

Database Links

HGNC: 28897

OMIM: 611750

KEGG: hsa:81493

STRING: 9606.ENSP00000386439

UniGene: Hs.712631

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Service

Phage Display Service

Antibody Service

Protein Service

Gene Synthesis Service

Oligo Synthesis Service

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301-363-4651 (Available 9 a.m. to 5 p.m. CST from Monday to Friday)

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Address

7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA

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