DNAH17 Polyclonal antibody

DNAH17 Polyclonal Antibody for WB, IHC, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human and More (1)

Applications

WB, IHC, IF, ELISA

Conjugate

Unconjugated

Cat no : 24488-1-AP

Synonyms

DNAH17, DNAHL1, DNEL2



Tested Applications

Positive WB detected inmouse testis tissue, rat testis tissue
Positive IHC detected inhuman kidney tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:500-1:1000
Immunohistochemistry (IHC)IHC : 1:20-1:200
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

24488-1-AP targets DNAH17 in WB, IHC, IF, ELISA applications and shows reactivity with human samples.

Tested Reactivity human
Cited Reactivityhuman, mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen DNAH17 fusion protein Ag20033
Full Name dynein, axonemal, heavy chain 17
Calculated Molecular Weight 4485 aa, 512 kDa
Observed Molecular Weight 500-512 kDa
GenBank Accession NumberBC112284
Gene Symbol DNAH17
Gene ID (NCBI) 8632
RRIDAB_2879568
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Protocols

Product Specific Protocols
WB protocol for DNAH17 antibody 24488-1-APDownload protocol
IHC protocol for DNAH17 antibody 24488-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
IF

Elife

DNAH3 deficiency causes flagellar inner dynein arm loss and male infertility in humans and mice

Authors - Xiang Wang
humanIF

Clin Genet

Loss-of-function mutation in DNAH8 induces asthenoteratospermia associated with multiple morphological abnormalities of the sperm flagella.

Authors - Yihong Yang
human,mouseIF

Reprod Biomed Online

A novel mutation in DNAH17 is present in a patient with multiple morphological abnormalities of the flagella.

Authors - Rui Zheng
human, mouseIF

J Assist Reprod Genet

The effect of a novel LRRC6 mutation on the flagellar ultrastructure in a primary ciliary dyskinesia patient.

Authors - Yaqian Li
humanWB,IF

Ann Hum Genet

DNAH17 is associated with asthenozoospermia and multiple morphological abnormalities of sperm flagella.

Authors - Yanwei Sha
humanIF

Hum Mol Genet

Population-based genetic analysis in infertile men reveals novel mutations of ADAD family members in patients with impaired spermatogenesis

Authors - Siyu Dai